Are you an accomplished QA Auditor with extensive experience of working within a GLP/GCP regulated facility? If so, this could be the role for you! Working in a dynamic and friendly laboratory you will be responsible for conducting study and process audits for a busy QA department. As a key member of the team you will ensure compliance to quality systems, undertaking regular audits of the facility and laboratory conduct. You will be fundamental in approving laboratory SOP's, protocols and reports, reviewing any changes and investigating any deviations. As a Senior member of the team you will hold additional responsibilities including staff supervision, maintenance of the current QA program and the development of quality management systems. You will also train staff on quality procedures and regulations. Applications are invited from accomplished Quality Auditors who have experience within a GLP/GCP regulated facility. If this sounds like the opportunity for you then apply to VRS today! Key words: Quality Manager, Quality Assurance, QA, GLP, GCP, GxP, Audit, analytical chemistry, Good Laboratory Practice, Dundee, VRS6331CR Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website.
18/06/2019
Are you an accomplished QA Auditor with extensive experience of working within a GLP/GCP regulated facility? If so, this could be the role for you! Working in a dynamic and friendly laboratory you will be responsible for conducting study and process audits for a busy QA department. As a key member of the team you will ensure compliance to quality systems, undertaking regular audits of the facility and laboratory conduct. You will be fundamental in approving laboratory SOP's, protocols and reports, reviewing any changes and investigating any deviations. As a Senior member of the team you will hold additional responsibilities including staff supervision, maintenance of the current QA program and the development of quality management systems. You will also train staff on quality procedures and regulations. Applications are invited from accomplished Quality Auditors who have experience within a GLP/GCP regulated facility. If this sounds like the opportunity for you then apply to VRS today! Key words: Quality Manager, Quality Assurance, QA, GLP, GCP, GxP, Audit, analytical chemistry, Good Laboratory Practice, Dundee, VRS6331CR Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website.
Are you a Computer Sceince Graduate already or graduating this year? Are you looking to springboard your career and utilise all you have learnt in a forward thinking, client facing environment? Research and Development could be the career path for you The company is looking to employ computer science graduates with a keen interest in industrial developments and technologies to work as junior consultants in R&D Incentives. The successful candidates will be joining a team of positive and driven R&D incentive specialists with diverse backgrounds in science, engineering, software and tax. Industry experience is a bonus but not essential. The role provides you with the opportunity to explore and write reports about evolving and applied technologies across an extremely wide range of industries with the overlaid challenge of ensuring that the reports are robust and satisfy the appropriate Legislation, Guidelines and in-turn the expectations of HMRC, who oversees the R&D incentive claims. At the same time you will have an opportunity to travel and meet with both large and small companies very early in your employment, which gives you first-hand experience of operations across many industries. The company values the development of employees and pays particular attention to their continual training and growth with a flexible approach to accommodating each individual's personal needs in the work place. Senior team members will actively take part in the training and mentoring of new employees. The role will build your skills in professional services associated with project management, formal and informal communication, people management, report writing and cost analysis. Some of the day-to-day activities and duties will include: Attend client R&D incentive meetings, communicate qualifying criteria and taking coherent and relevant notes Build and develop working relationships with colleagues, clients and other third parties to develop further opportunities and business Identification and analysis of qualifying R&D projects, activities and expenditure ensuring R&D claims meet the requirements of relevant tax Legislation and Guidelines Apply R&D tax Legislation and BEIS Guidelines in assessing a diverse range of industries and fields Writing science and engineering technical descriptions and claim reports to present in a suitable format for HMRC Prepare R&D claim cost calculations and associated summaries of the method of assessment Liaise with internal and external finance and technical teams to ensure incentive claims are delivered accurately and on time Where enquiries are opened by HMRC, contribute to achieving a resolution Continuously develop own knowledge & skills and keep up to date on technical and financial knowledge Qualifications and skills Degree in computer science/software or related Highly motivated Excellent verbal and written communication skills Ability to learn quickly and independently Comfortable with excel for an informal chat please forward your CV
18/06/2019
Are you a Computer Sceince Graduate already or graduating this year? Are you looking to springboard your career and utilise all you have learnt in a forward thinking, client facing environment? Research and Development could be the career path for you The company is looking to employ computer science graduates with a keen interest in industrial developments and technologies to work as junior consultants in R&D Incentives. The successful candidates will be joining a team of positive and driven R&D incentive specialists with diverse backgrounds in science, engineering, software and tax. Industry experience is a bonus but not essential. The role provides you with the opportunity to explore and write reports about evolving and applied technologies across an extremely wide range of industries with the overlaid challenge of ensuring that the reports are robust and satisfy the appropriate Legislation, Guidelines and in-turn the expectations of HMRC, who oversees the R&D incentive claims. At the same time you will have an opportunity to travel and meet with both large and small companies very early in your employment, which gives you first-hand experience of operations across many industries. The company values the development of employees and pays particular attention to their continual training and growth with a flexible approach to accommodating each individual's personal needs in the work place. Senior team members will actively take part in the training and mentoring of new employees. The role will build your skills in professional services associated with project management, formal and informal communication, people management, report writing and cost analysis. Some of the day-to-day activities and duties will include: Attend client R&D incentive meetings, communicate qualifying criteria and taking coherent and relevant notes Build and develop working relationships with colleagues, clients and other third parties to develop further opportunities and business Identification and analysis of qualifying R&D projects, activities and expenditure ensuring R&D claims meet the requirements of relevant tax Legislation and Guidelines Apply R&D tax Legislation and BEIS Guidelines in assessing a diverse range of industries and fields Writing science and engineering technical descriptions and claim reports to present in a suitable format for HMRC Prepare R&D claim cost calculations and associated summaries of the method of assessment Liaise with internal and external finance and technical teams to ensure incentive claims are delivered accurately and on time Where enquiries are opened by HMRC, contribute to achieving a resolution Continuously develop own knowledge & skills and keep up to date on technical and financial knowledge Qualifications and skills Degree in computer science/software or related Highly motivated Excellent verbal and written communication skills Ability to learn quickly and independently Comfortable with excel for an informal chat please forward your CV
International Pharmaceutical Manufacturer seeks a Sterility Assurance Support Officer. About the role: A Sterility Assurance Support Officer is responsible for trending and reviewing microbiological out-of-limits data; for coordinating the MEMR and sterility assurance meetings; for raising and assessing CAPA action items; for raising and tracking process impact assessments; and for tracking investigation responses. Occasional visits to process areas, including aseptic processing facilities is required. Duties may include: To operate a system for trending all microbiology investigations and deviations and to report out this information on a weekly basis. This involves using Trackwise, designing spreadsheets and producing trend charts. To organise, schedule, draw up agendas, minute, raise corrective and preventative actions for the microbiological data review meeting and the sterility assurance governance committee. To oversee CAPAs pertaining to sterility assurance and to support the closure of items. To use Trackwise and other electronic document systems. To devise and operate spreadsheets. To type and collate reports. To undertake scanning and archiving. To review and raise process impact events relating to production activities, by following pre-defined schematics. To offer support to the Sterility Assurance team with investigations. To occasionally visit process areas to assist the Sterility Assurance Team with investigations (e.g. taking notes at meetings, taking digital images). To write summary reports relating to sterility assurance issues. To manage the Sterility Assurance documentation, files and directories. To produce data trend reports in graphical and statistical formats. To assist in overseeing the upkeep of staff competencies and training To input and export data, through the use of spreadsheets, databased and LIMS. To update documents and SOPs as required. To input into continuous improvement initiatives. To perform any other tasks requested by the Sterility Assurance Manager. Skills and experience: Understanding of GMP and Quality Assurance. Understanding of pharmaceutical microbiology. Understanding of pharmaceutical processing. Creating and revising documentation Degree in scientific subject Competency in data management Certification in MS office
18/06/2019
International Pharmaceutical Manufacturer seeks a Sterility Assurance Support Officer. About the role: A Sterility Assurance Support Officer is responsible for trending and reviewing microbiological out-of-limits data; for coordinating the MEMR and sterility assurance meetings; for raising and assessing CAPA action items; for raising and tracking process impact assessments; and for tracking investigation responses. Occasional visits to process areas, including aseptic processing facilities is required. Duties may include: To operate a system for trending all microbiology investigations and deviations and to report out this information on a weekly basis. This involves using Trackwise, designing spreadsheets and producing trend charts. To organise, schedule, draw up agendas, minute, raise corrective and preventative actions for the microbiological data review meeting and the sterility assurance governance committee. To oversee CAPAs pertaining to sterility assurance and to support the closure of items. To use Trackwise and other electronic document systems. To devise and operate spreadsheets. To type and collate reports. To undertake scanning and archiving. To review and raise process impact events relating to production activities, by following pre-defined schematics. To offer support to the Sterility Assurance team with investigations. To occasionally visit process areas to assist the Sterility Assurance Team with investigations (e.g. taking notes at meetings, taking digital images). To write summary reports relating to sterility assurance issues. To manage the Sterility Assurance documentation, files and directories. To produce data trend reports in graphical and statistical formats. To assist in overseeing the upkeep of staff competencies and training To input and export data, through the use of spreadsheets, databased and LIMS. To update documents and SOPs as required. To input into continuous improvement initiatives. To perform any other tasks requested by the Sterility Assurance Manager. Skills and experience: Understanding of GMP and Quality Assurance. Understanding of pharmaceutical microbiology. Understanding of pharmaceutical processing. Creating and revising documentation Degree in scientific subject Competency in data management Certification in MS office
Machine Learning Engineer Pioneering Medical Devices business. Central Bristol offices with excellent transport links. Work on patented technology that will change the lives of millions. Would you like to join an innovative company, using cutting-edge technology with the aim to make a real difference in people's lives? If that sounds like the role for you, I'm currently working with a Medical Devices company based in Bristol who'd be keen to speak with you. What you'll be doing The company is at the forefront of their field and in the process of developing a product that will revolutionise disease screening. This role will primarily involve the creation and deployment of Machine Learning models to help support the development of the company's applications. You'll be able to get involved in a wide range of activities and give you the opportunity to learn a great deal working with colleagues who are experts in their field. This is a broad role with the chance to get stuck in with a range to tools and technologies. What experience you'll need to apply A Masters or PhD in a technology related field (e.g. Computer Science, STEM or Engineering etc.) Experience building deep learning models and scalable machine learning systems. Programming skills in Python, Matlab or R. Experience with either Ultrasound, MRI or CT imaging would be very beneficial. Communication skills are key in this one as you'll be interacting with people across the business as well as stakeholders outside of it. What you'll get in return for your experience The salary on this one is between £40K - £50K alongside a great working environment with a supportive and knowledgeable team. You'll also be working at the forefront of some truly novel technology that will change the lives of millions. There will also be the opportunity to really grow into the role with clear career progression opportunities. What next? If this sounds like the role for you, get in touch with Adam with your updated CV and we'll handle the rest.
18/06/2019
Machine Learning Engineer Pioneering Medical Devices business. Central Bristol offices with excellent transport links. Work on patented technology that will change the lives of millions. Would you like to join an innovative company, using cutting-edge technology with the aim to make a real difference in people's lives? If that sounds like the role for you, I'm currently working with a Medical Devices company based in Bristol who'd be keen to speak with you. What you'll be doing The company is at the forefront of their field and in the process of developing a product that will revolutionise disease screening. This role will primarily involve the creation and deployment of Machine Learning models to help support the development of the company's applications. You'll be able to get involved in a wide range of activities and give you the opportunity to learn a great deal working with colleagues who are experts in their field. This is a broad role with the chance to get stuck in with a range to tools and technologies. What experience you'll need to apply A Masters or PhD in a technology related field (e.g. Computer Science, STEM or Engineering etc.) Experience building deep learning models and scalable machine learning systems. Programming skills in Python, Matlab or R. Experience with either Ultrasound, MRI or CT imaging would be very beneficial. Communication skills are key in this one as you'll be interacting with people across the business as well as stakeholders outside of it. What you'll get in return for your experience The salary on this one is between £40K - £50K alongside a great working environment with a supportive and knowledgeable team. You'll also be working at the forefront of some truly novel technology that will change the lives of millions. There will also be the opportunity to really grow into the role with clear career progression opportunities. What next? If this sounds like the role for you, get in touch with Adam with your updated CV and we'll handle the rest.
Our client is a development and commercialisation organisation that specialises in materials technologies and processes. They looking for an experienced Analytical Chemist to lead the day to day running of their Organic Chemistry lab and be responsible for the running of routine samples. A degree in Chemistry (or equivalent) along with at least 5 years' experience working in an analytical laboratory is essential. Key responsibilities will include: Deputising for the Chemistry Delivery Manager (for organic lab) as required Routine gas analysis using a GC thermal desorption system Maintenance of QC charts for the gas analysis Authorising of results Development of gas analysis methods, re-writing/updating methods and further validation as required Accurate production of calibration standards for GCMS analysis Calibration of equipment GCMS maintenance and supervision of engineers Reviewing quotations Writing and reviewing reports Skills/experience required: Ability to follow scientific methods accurately and offer ideas for improvements Experience of GC-MS, GC-FID, HPLC, GPC Experience of supervising junior members of staff Experience of analytical method development and validation Experience of working in an ISO 17025 or Mcerts accredited laboratory Some experience of the analysis of medical devices, toys or materials for organic residues would be desirable Will have previously worked in a laboratory using quality control charts and will know how to maintain the QC charts if required Ability to work well as part of a team We will endeavour to respond to your contact/application within 48 hours, but due to the volume of applications we receive on a daily basis, if you haven't heard from us within 4 working days, please consider your application unsuccessful. This advert has been posted by a recruitment agency acting on behalf of a client.
18/06/2019
Our client is a development and commercialisation organisation that specialises in materials technologies and processes. They looking for an experienced Analytical Chemist to lead the day to day running of their Organic Chemistry lab and be responsible for the running of routine samples. A degree in Chemistry (or equivalent) along with at least 5 years' experience working in an analytical laboratory is essential. Key responsibilities will include: Deputising for the Chemistry Delivery Manager (for organic lab) as required Routine gas analysis using a GC thermal desorption system Maintenance of QC charts for the gas analysis Authorising of results Development of gas analysis methods, re-writing/updating methods and further validation as required Accurate production of calibration standards for GCMS analysis Calibration of equipment GCMS maintenance and supervision of engineers Reviewing quotations Writing and reviewing reports Skills/experience required: Ability to follow scientific methods accurately and offer ideas for improvements Experience of GC-MS, GC-FID, HPLC, GPC Experience of supervising junior members of staff Experience of analytical method development and validation Experience of working in an ISO 17025 or Mcerts accredited laboratory Some experience of the analysis of medical devices, toys or materials for organic residues would be desirable Will have previously worked in a laboratory using quality control charts and will know how to maintain the QC charts if required Ability to work well as part of a team We will endeavour to respond to your contact/application within 48 hours, but due to the volume of applications we receive on a daily basis, if you haven't heard from us within 4 working days, please consider your application unsuccessful. This advert has been posted by a recruitment agency acting on behalf of a client.
Future Select Ltd
33 Windsor Pl, Cardiff CF10 3BZ, UK
An asbestos consultancy that offers professional advice and support services on a wide range of asbestos and environmental disciplines presently requires a tenacious and self-motivated Asbestos Lab Analyst to join their busy team/laboratory in South Wales and will include applications from Caerphilly, Newport, Cardiff and the surrounding areas. Qualifications & Experience: The applicant must possess the Asbestos P401 certificate and at the same must have prior and relevant experience working within the laboratory environment and within the asbestos industry. Must have excellent communication skills, both written and verbal and proficient in using the Microsoft Office Package. The main focus of the role is to analyze and report on the fibre content of both of samples submitted by clients. Specific Aspects of the Role: Receiving and appropriately logging samples received by the laboratory, preparing samples for analysis, carrying out analysis of samples for fibre content and reporting analytical findings. Completing analysis test sheets as and when required and ensuring every effort to complete workload within required time frame. Getting involved with other laboratory and ad-hoc duties. The successful applicant must be articulate, flexible, have good attention to detail and have the ability to carry out the work within time frame. A good salary, depending on expertise and along with many other benefits awaits the right candidate. Future Select are the leading market supplier for recruitment in the Asbestos industry, we work with the best clients & candidates and supply the majority of permanent jobs in the asbestos market. We have a large dedicated team, with over 25 years combined industry experience within Asbestos recruitment specifically geared to dealing with Asbestos Surveyors/Analysts/Lab Technicians, Administrators, Project/Regional /Technical/Quality/Training/Sales Managers through to Director level for both Consultancy & Removal. We have intrinsic knowledge of the market place, as well as respecting candidates/clients confidentiality in this close knit market sector. We are also interested in anyone with p401/p402/p403/p404/p404 or s301 CCP. We are inundated with applications, we will endeavour to get back in touch, however if you have applied to Future Select and you have not heard from us after a week, on this occasion, you will not have been successful. Your details will be saved on our system and you will be contacted in the future if a vacancy matches your skills. Future Select Copyright 2019.
18/06/2019
An asbestos consultancy that offers professional advice and support services on a wide range of asbestos and environmental disciplines presently requires a tenacious and self-motivated Asbestos Lab Analyst to join their busy team/laboratory in South Wales and will include applications from Caerphilly, Newport, Cardiff and the surrounding areas. Qualifications & Experience: The applicant must possess the Asbestos P401 certificate and at the same must have prior and relevant experience working within the laboratory environment and within the asbestos industry. Must have excellent communication skills, both written and verbal and proficient in using the Microsoft Office Package. The main focus of the role is to analyze and report on the fibre content of both of samples submitted by clients. Specific Aspects of the Role: Receiving and appropriately logging samples received by the laboratory, preparing samples for analysis, carrying out analysis of samples for fibre content and reporting analytical findings. Completing analysis test sheets as and when required and ensuring every effort to complete workload within required time frame. Getting involved with other laboratory and ad-hoc duties. The successful applicant must be articulate, flexible, have good attention to detail and have the ability to carry out the work within time frame. A good salary, depending on expertise and along with many other benefits awaits the right candidate. Future Select are the leading market supplier for recruitment in the Asbestos industry, we work with the best clients & candidates and supply the majority of permanent jobs in the asbestos market. We have a large dedicated team, with over 25 years combined industry experience within Asbestos recruitment specifically geared to dealing with Asbestos Surveyors/Analysts/Lab Technicians, Administrators, Project/Regional /Technical/Quality/Training/Sales Managers through to Director level for both Consultancy & Removal. We have intrinsic knowledge of the market place, as well as respecting candidates/clients confidentiality in this close knit market sector. We are also interested in anyone with p401/p402/p403/p404/p404 or s301 CCP. We are inundated with applications, we will endeavour to get back in touch, however if you have applied to Future Select and you have not heard from us after a week, on this occasion, you will not have been successful. Your details will be saved on our system and you will be contacted in the future if a vacancy matches your skills. Future Select Copyright 2019.
Pharmaceutical Project Manager Location: Oxfordshire Sector: Pharmaceutical Our client is a leading Pharmaceutical CRO based in Oxfordshire and is now seeking an experienced Project Manager to support with the leadership and management of projects while promoting continuous improvement and a high level service to clients. The role: As a Project Manager you will be responsible for continuous communication and project co-ordination across a range of business departments. Working closely with clients you will provide a high standard of service and act as the liaison between the client and the relevant departments. The role will require active involvement in project proposals, monitoring of timelines & project progress, establishing budgets, drive project communication between client & technical team, facilitate necessary project meetings and overcome and resolve project challenges. Experience expectations: Suitable applicants will have; Previous experience working in a Project Management role within the Pharmaceutical sector. Experience working with project proposals and management of project timelines Educated to degree level (or equivalent experience) in a relevant Chemistry discipline Experience working within a GMP environment Excellent communication skills and attention to detail Good knowledge of MS Office programs The Package: Our client offers an opportunity to work for a leading Pharmaceutical company on a permanent basis with a competitive annual salary and benefits package.
18/06/2019
Pharmaceutical Project Manager Location: Oxfordshire Sector: Pharmaceutical Our client is a leading Pharmaceutical CRO based in Oxfordshire and is now seeking an experienced Project Manager to support with the leadership and management of projects while promoting continuous improvement and a high level service to clients. The role: As a Project Manager you will be responsible for continuous communication and project co-ordination across a range of business departments. Working closely with clients you will provide a high standard of service and act as the liaison between the client and the relevant departments. The role will require active involvement in project proposals, monitoring of timelines & project progress, establishing budgets, drive project communication between client & technical team, facilitate necessary project meetings and overcome and resolve project challenges. Experience expectations: Suitable applicants will have; Previous experience working in a Project Management role within the Pharmaceutical sector. Experience working with project proposals and management of project timelines Educated to degree level (or equivalent experience) in a relevant Chemistry discipline Experience working within a GMP environment Excellent communication skills and attention to detail Good knowledge of MS Office programs The Package: Our client offers an opportunity to work for a leading Pharmaceutical company on a permanent basis with a competitive annual salary and benefits package.
This is a new permanent job opportunity for an Information Scientist, to be based in Gloucestershire. You will join an existing Library, Information and Research team in providing a range of information services. This will include answering enquiries, research, literature searching and business intelligence. You will support clients and work to build the technical knowledge base. You will be happy dealing directly with clients regarding either subscription services or running webex demonstrations, etc. This job role will also help to monitor the latest technical information management applications that support information provision. Key job requirements include: A degree qualification in Information Science or similar, accredited by CILIP An understanding of database, search and content management systems The ability to search and disseminate technical information Excellent IT skills and an awareness of the latest techniques and technologies being used to provide information Strong communication and client skills Strong report writing and presentation skills Ideally you will have some experience of information provision in a commercial organisation, but applications are also welcomed from new Library/Information graduates. This is a great opportunity to join an Information Services team in a specialist sector, and to be based in Gloucestershire (a driver) and happy to travel to the Surrey office. To be considered for this and other Information Management job opportunities please apply with your CV to
18/06/2019
This is a new permanent job opportunity for an Information Scientist, to be based in Gloucestershire. You will join an existing Library, Information and Research team in providing a range of information services. This will include answering enquiries, research, literature searching and business intelligence. You will support clients and work to build the technical knowledge base. You will be happy dealing directly with clients regarding either subscription services or running webex demonstrations, etc. This job role will also help to monitor the latest technical information management applications that support information provision. Key job requirements include: A degree qualification in Information Science or similar, accredited by CILIP An understanding of database, search and content management systems The ability to search and disseminate technical information Excellent IT skills and an awareness of the latest techniques and technologies being used to provide information Strong communication and client skills Strong report writing and presentation skills Ideally you will have some experience of information provision in a commercial organisation, but applications are also welcomed from new Library/Information graduates. This is a great opportunity to join an Information Services team in a specialist sector, and to be based in Gloucestershire (a driver) and happy to travel to the Surrey office. To be considered for this and other Information Management job opportunities please apply with your CV to
Robotics and Automation Consultant - Client Facing - Cambridge A growing Robotics and Automation team, based in Cambridge, are currently looking for a Robotics and Automation Consultant to help with client facing meetings where you will have technical discussions on new robotics an automation application of technology. As mentioned, your discussions will be from a technical viewpoint, due to this you will need to have developed into a client facing role from a pervious technical role. Ideally, you will need to have been an electronics engineer, mechanical engineer, machine learning, physicist or other hands on technical role that involved developing robotic, automation or another complex field closely linked. It is expected that you would hold a degree within a relevant technical field. As robotics and automation is quite a new technology, we are not expecting you to have had years and years of experience in the field, however the last few years of your career would be essential. If you also hold a PhD this would be advantageous, but not essential. After meeting with clients and finding out their requirements, you will need to relay this information back to the technical teams who will implement the projects. Your role will essentially continue into the project management of complex projects. Your industry experience, over the last few years, will help you identify key stakeholders in 3rd party organisations. We are open to applications from experienced Robotics or Automation Consultants, experienced Business Development experts from the field of Robotics/Automation and a technical background and we will also look at a technical individual who has the ambition of moving into a client facing role. This is a very unique role in a very exciting field, due to this I expect quite a lot of interest. If you are interested, I'd suggest making an application now or risk missing out. For more information, please feel free to call Andrew Welsh, Director of Medical Devices recruitment and Scientific recruitment specialists Newton Colmore Consulting, on + or make an application and one of our team at Newton Colmore Consulting will contact you. Newton Colmore Consulting is a specialist recruitment company within the Medical Devices, Scientific Engineering, Data Science, Machine Learning, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance and Field Service Engineering sectors.
18/06/2019
Robotics and Automation Consultant - Client Facing - Cambridge A growing Robotics and Automation team, based in Cambridge, are currently looking for a Robotics and Automation Consultant to help with client facing meetings where you will have technical discussions on new robotics an automation application of technology. As mentioned, your discussions will be from a technical viewpoint, due to this you will need to have developed into a client facing role from a pervious technical role. Ideally, you will need to have been an electronics engineer, mechanical engineer, machine learning, physicist or other hands on technical role that involved developing robotic, automation or another complex field closely linked. It is expected that you would hold a degree within a relevant technical field. As robotics and automation is quite a new technology, we are not expecting you to have had years and years of experience in the field, however the last few years of your career would be essential. If you also hold a PhD this would be advantageous, but not essential. After meeting with clients and finding out their requirements, you will need to relay this information back to the technical teams who will implement the projects. Your role will essentially continue into the project management of complex projects. Your industry experience, over the last few years, will help you identify key stakeholders in 3rd party organisations. We are open to applications from experienced Robotics or Automation Consultants, experienced Business Development experts from the field of Robotics/Automation and a technical background and we will also look at a technical individual who has the ambition of moving into a client facing role. This is a very unique role in a very exciting field, due to this I expect quite a lot of interest. If you are interested, I'd suggest making an application now or risk missing out. For more information, please feel free to call Andrew Welsh, Director of Medical Devices recruitment and Scientific recruitment specialists Newton Colmore Consulting, on + or make an application and one of our team at Newton Colmore Consulting will contact you. Newton Colmore Consulting is a specialist recruitment company within the Medical Devices, Scientific Engineering, Data Science, Machine Learning, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance and Field Service Engineering sectors.
Job t itle: Customer Segmentation Manager Location: London Salary: Circa £55'000 - £60'000 (Poss more for the right person) Contract: Full time, Permanent Overview: Customer Management Resourcing (CMR) is a boutique recruitment consultancy that specialise in mid & executive level roles within 'Customer Management'. This includes all management or analytical roles surrounding Contact Centres, Customer Experience & A.I. We are proud to be working with a leading, well established international travel organisation based in London in their search for a new Customer Segmentation Manager. Scope of the role: The Customer Segmentation Manager will develop the customer segmentation efforts at both a macro and micro level; enabling the core business areas to utilise this and better understand customer behaviours. You will be responsible for progressing and leading the organisation's efforts around understanding and segmenting our customers in order to optimise products and experiences to be tailored to each customer's needs. This is an exciting new role based in central London reporting to the Head of Data, Insight & Analytics. It will support departments across the business with questions they have around our customers. Main Responsibilities: Develop the organisation's customer understanding at a macro and micro level as well as segment the customer base in different ways to meet business needs. Utilise behavioural, demographic, geographical & attitudinal / psychographic data to design, build, develop and maintain segmentations and other statistical models to analyse customer audiences and behaviours. Ensure that segments are relevant, distinguishable, sizeable and locatable and work with the IS team to make this data available to wider systems to act as triggers and identifiers to drive customer targeting and contact strategies. Develop processes to capture customer related data from both internal and external sources so we build up as detailed a profile as practical on each customer. Produce best in class visualisations and self-service dashboards in Tableau to help stakeholders understand customer behaviours and patterns. Provide analytical support to business teams for questions around customer data, identifying the best way to provide these answers and enabling self-service to elements where regular reporting is required. Person Specification: A degree in statistics, mathematics, science or similar. A proven track record of analysing data sets and providing clear recommendations back to stakeholders. A minimum of three years' experience in a similar analytical role, including previous working experience using different statistical models to segment customers. Proficiency with using SQL (advanced joins, string functions, regex) and experience dealing with large, complex datasets of different varieties (e.g. transactional data, digital data, survey response data, marketing data). Significant experience of applying statistical, analytical, modelling and segmentation techniques (including packages such as R, Python, SAS or SPSS). The ability to present complex information in a simple and effective way. Benefits/ Remuneration: Salary range of circa £55k - £60k (negotiable for the right person) Travel benefits for work and play A great pension Exclusive discounts and perks How to apply: To be considered for this opportunity or for more information, you will need to email an updated CV to Nichola We do endeavour to respond to as many applications as possible, however due to the high volume of applications we tend to receive we cannot always advise each individual unsuccessful applicant. If you haven't heard from us within 14 days of submitting your application, please assume that on this occasion you have been unsuccessful.
18/06/2019
Job t itle: Customer Segmentation Manager Location: London Salary: Circa £55'000 - £60'000 (Poss more for the right person) Contract: Full time, Permanent Overview: Customer Management Resourcing (CMR) is a boutique recruitment consultancy that specialise in mid & executive level roles within 'Customer Management'. This includes all management or analytical roles surrounding Contact Centres, Customer Experience & A.I. We are proud to be working with a leading, well established international travel organisation based in London in their search for a new Customer Segmentation Manager. Scope of the role: The Customer Segmentation Manager will develop the customer segmentation efforts at both a macro and micro level; enabling the core business areas to utilise this and better understand customer behaviours. You will be responsible for progressing and leading the organisation's efforts around understanding and segmenting our customers in order to optimise products and experiences to be tailored to each customer's needs. This is an exciting new role based in central London reporting to the Head of Data, Insight & Analytics. It will support departments across the business with questions they have around our customers. Main Responsibilities: Develop the organisation's customer understanding at a macro and micro level as well as segment the customer base in different ways to meet business needs. Utilise behavioural, demographic, geographical & attitudinal / psychographic data to design, build, develop and maintain segmentations and other statistical models to analyse customer audiences and behaviours. Ensure that segments are relevant, distinguishable, sizeable and locatable and work with the IS team to make this data available to wider systems to act as triggers and identifiers to drive customer targeting and contact strategies. Develop processes to capture customer related data from both internal and external sources so we build up as detailed a profile as practical on each customer. Produce best in class visualisations and self-service dashboards in Tableau to help stakeholders understand customer behaviours and patterns. Provide analytical support to business teams for questions around customer data, identifying the best way to provide these answers and enabling self-service to elements where regular reporting is required. Person Specification: A degree in statistics, mathematics, science or similar. A proven track record of analysing data sets and providing clear recommendations back to stakeholders. A minimum of three years' experience in a similar analytical role, including previous working experience using different statistical models to segment customers. Proficiency with using SQL (advanced joins, string functions, regex) and experience dealing with large, complex datasets of different varieties (e.g. transactional data, digital data, survey response data, marketing data). Significant experience of applying statistical, analytical, modelling and segmentation techniques (including packages such as R, Python, SAS or SPSS). The ability to present complex information in a simple and effective way. Benefits/ Remuneration: Salary range of circa £55k - £60k (negotiable for the right person) Travel benefits for work and play A great pension Exclusive discounts and perks How to apply: To be considered for this opportunity or for more information, you will need to email an updated CV to Nichola We do endeavour to respond to as many applications as possible, however due to the high volume of applications we tend to receive we cannot always advise each individual unsuccessful applicant. If you haven't heard from us within 14 days of submitting your application, please assume that on this occasion you have been unsuccessful.
A multi-national and leading speciality chemical business based in Berkshire is currently seeking a Toxicologist to join their EHS department on a permanent basis. As Toxicologist, you will play a key role in developing, interpreting and communicating toxicological data to provide product stewardship support and ensure strict compliances are met. Toxicologist Responsibilities Develop, implement, and lead process to identify and classify human health and/or environmental hazards of chemicals associated with chemical products. Qualify and manage contracts with outside toxicology test labs. Customise protocols to accommodate the properties of the material. Prepare design, review, evaluate, and interpret toxicology test results (mammalian and eco-tox) related to substances of interest to the company. Prepare toxicological summaries and calculations for substance and product registration globally. Interact with regulatory agencies on toxicology matters related to new regulation and product registration. Assemble, review and interpret data from literature, testing, chemical grouping, and modelling used as a basis for development of our SDS toxicity and classification statements. Monitor on an on-going basis. Participate on industry trade associations, technical workgroups, and scientific/regulatory advocacy committees that address toxicology issues of interest to the company. Toxicologist Requirements You must possess a degree level qualification in Toxicology, pharmacology, chemistry or life sciences. To possess experience in the toxicology field or equivalent combination of education and experience. If you demonstrate an understanding with both ecotoxicology and mammalian toxicology - this will be highly desirable. Strong communicator with the ability to translate complex scientific data and information into understandable language that facilitates business decision making. Ability to collaborate with internal and external stakeholders. Possesses sound judgment, excellent analytical and problem-solving skills and has the inner confidence to take risks and make tough calls. £ Competitive Salary + Excellent Benefits Package (Incl. Final Salary Pension Scheme, Healthcare etc.)
18/06/2019
A multi-national and leading speciality chemical business based in Berkshire is currently seeking a Toxicologist to join their EHS department on a permanent basis. As Toxicologist, you will play a key role in developing, interpreting and communicating toxicological data to provide product stewardship support and ensure strict compliances are met. Toxicologist Responsibilities Develop, implement, and lead process to identify and classify human health and/or environmental hazards of chemicals associated with chemical products. Qualify and manage contracts with outside toxicology test labs. Customise protocols to accommodate the properties of the material. Prepare design, review, evaluate, and interpret toxicology test results (mammalian and eco-tox) related to substances of interest to the company. Prepare toxicological summaries and calculations for substance and product registration globally. Interact with regulatory agencies on toxicology matters related to new regulation and product registration. Assemble, review and interpret data from literature, testing, chemical grouping, and modelling used as a basis for development of our SDS toxicity and classification statements. Monitor on an on-going basis. Participate on industry trade associations, technical workgroups, and scientific/regulatory advocacy committees that address toxicology issues of interest to the company. Toxicologist Requirements You must possess a degree level qualification in Toxicology, pharmacology, chemistry or life sciences. To possess experience in the toxicology field or equivalent combination of education and experience. If you demonstrate an understanding with both ecotoxicology and mammalian toxicology - this will be highly desirable. Strong communicator with the ability to translate complex scientific data and information into understandable language that facilitates business decision making. Ability to collaborate with internal and external stakeholders. Possesses sound judgment, excellent analytical and problem-solving skills and has the inner confidence to take risks and make tough calls. £ Competitive Salary + Excellent Benefits Package (Incl. Final Salary Pension Scheme, Healthcare etc.)
Experiment Preforming Physicist - Cambridge A truly exciting role has become available for an established spin-out company. Your role as a Physicist will involve creating and preforming experiments to help with the development of new technologies and the improvement of current generation technologies. Due to the hands-on nature of this work you will ideally have been working in industry or on a successful product development during your PhD and post-doc work. We are open to you having worked on a wide range of different technologies, however the easiest transferable technologies would include microfluidics, semiconductors, printed electronics, microfabrication, electrostatic or other fluidic based technologies. It is just as important to find someone who would fit into the culture of the organisation, ideally you will have a pro-active approach and enjoy working on challenging problems. Ideally, you will hold a PhD however is you do not hold a degree but have a number of years of successful experience as a Physicist we are still interested to hear from you. As this is a vital role for the company, we are open to people who have just finished their PhD or people with a number of years of industry experience. This will be a challenging role for you that will also offer you the chance to continually improve on your knowledge and skills. When successful in this role, you will be rewarded with an excellent salary and benefits package. Relocation allowance could also be available for the right person. Apart from the physical work as a Physicist, it would also be ideal if you have strong MATLAB exposure. I expect a lot of interest in this role, so if you are interested please make an application now or risk missing out. For more information, please feel free to call Andrew Welsh, Director of Medical Devices recruitment and Scientific recruitment specialists Newton Colmore Consulting, on + or make an application and one of our team at Newton Colmore Consulting will contact you. Newton Colmore Consulting is a specialist recruitment company within the Medical Devices, Scientific Engineering, Data Science, Machine Learning, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance and Field Service Engineering sectors.
18/06/2019
Experiment Preforming Physicist - Cambridge A truly exciting role has become available for an established spin-out company. Your role as a Physicist will involve creating and preforming experiments to help with the development of new technologies and the improvement of current generation technologies. Due to the hands-on nature of this work you will ideally have been working in industry or on a successful product development during your PhD and post-doc work. We are open to you having worked on a wide range of different technologies, however the easiest transferable technologies would include microfluidics, semiconductors, printed electronics, microfabrication, electrostatic or other fluidic based technologies. It is just as important to find someone who would fit into the culture of the organisation, ideally you will have a pro-active approach and enjoy working on challenging problems. Ideally, you will hold a PhD however is you do not hold a degree but have a number of years of successful experience as a Physicist we are still interested to hear from you. As this is a vital role for the company, we are open to people who have just finished their PhD or people with a number of years of industry experience. This will be a challenging role for you that will also offer you the chance to continually improve on your knowledge and skills. When successful in this role, you will be rewarded with an excellent salary and benefits package. Relocation allowance could also be available for the right person. Apart from the physical work as a Physicist, it would also be ideal if you have strong MATLAB exposure. I expect a lot of interest in this role, so if you are interested please make an application now or risk missing out. For more information, please feel free to call Andrew Welsh, Director of Medical Devices recruitment and Scientific recruitment specialists Newton Colmore Consulting, on + or make an application and one of our team at Newton Colmore Consulting will contact you. Newton Colmore Consulting is a specialist recruitment company within the Medical Devices, Scientific Engineering, Data Science, Machine Learning, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance and Field Service Engineering sectors.
Information Scientist £25,000 - £30,000 Evesham or Redhill This established science and technology organisation is seeking an Information Scientist to join their team. This is a great opportunity for someone who has experience of information management and is looking to step into a role where they can put their stamp on the services offered. Duties will include: Work on projects to improve information gathering, dissemination and compilation. Help to develop new information services internally and externally. Use intelligence tools to extract information from a range of media and databases. Recommend and implement changes in services and products. Help to promote department services. Be a subject matter expert. Skills and Experience Required: Graduate or Postgraduate qualification in Information Science or similar, accredited by CILIP or similar. Excellent awareness of current information science practice and technology. Practical experience of database, search and information management/ Ability to search, extract and summarise technical information. Good communicator. For immediate consideration, please send your CV to today. We like to speak to every application, but due to the current climate this is not always possible. To ensure your application is not overlooked it is important that you emphasize any skills or work experience relevant to this position. If you have not heard from us within 5 working days please assume that you have been unsuccessful in this instance. i2i Recruitment Ltd is a leading independent employment agency providing staffing solutions across specialist areas. We are dedicated to provide a professional quality of service to clients and candidates alike.
18/06/2019
Information Scientist £25,000 - £30,000 Evesham or Redhill This established science and technology organisation is seeking an Information Scientist to join their team. This is a great opportunity for someone who has experience of information management and is looking to step into a role where they can put their stamp on the services offered. Duties will include: Work on projects to improve information gathering, dissemination and compilation. Help to develop new information services internally and externally. Use intelligence tools to extract information from a range of media and databases. Recommend and implement changes in services and products. Help to promote department services. Be a subject matter expert. Skills and Experience Required: Graduate or Postgraduate qualification in Information Science or similar, accredited by CILIP or similar. Excellent awareness of current information science practice and technology. Practical experience of database, search and information management/ Ability to search, extract and summarise technical information. Good communicator. For immediate consideration, please send your CV to today. We like to speak to every application, but due to the current climate this is not always possible. To ensure your application is not overlooked it is important that you emphasize any skills or work experience relevant to this position. If you have not heard from us within 5 working days please assume that you have been unsuccessful in this instance. i2i Recruitment Ltd is a leading independent employment agency providing staffing solutions across specialist areas. We are dedicated to provide a professional quality of service to clients and candidates alike.
Recruitment Consultant Life Sciences Salary: £18,000.00 to £60,000.00 /year 1 OTE Location: Redhill, Surrey Albion Rye Associates are an independent and privately owned recruitment agency based in smart quirky offices in Redhill town center. Having recently completed a successful first year of trading, we are seeking a motivated and driven consultant to become team member number 3. Offering an excellent work life balance, good working environment, table tennis table and an office dog (if that's what you look for)... but more importantly a blank canvass We are currently recruiting solely in Healthcare Communications, Medical Affairs and some Commercial roles, all other areas are untouched (no reputation smashes a poor one all day long). Looking for knowledge and expertise in: Regulatory Affairs / Quality Assurance Medical Devices Commercial Scientific / Laboratory Medical Affairs Clinical Research You will have: LinkedIn recruiter Job boards Freedom to meet clients and candidates Attendance to events where possible Free reign to build your own mini empire Globally recruiting freedom (US, ASIA, EUROPE) Excellent commission structure and a chance to really work SMART in a way. If you want to know more, drop me a note on LinkedIn, JAKE BYRNE or send your CV (let's face it, we all look at CV's enough to not bother sometimes with our own). Let's grab a beer and see what the future holds. Job Type: Full-time Salary: £18,000.00 to £60,000.00 /year 1 OTE
18/06/2019
Recruitment Consultant Life Sciences Salary: £18,000.00 to £60,000.00 /year 1 OTE Location: Redhill, Surrey Albion Rye Associates are an independent and privately owned recruitment agency based in smart quirky offices in Redhill town center. Having recently completed a successful first year of trading, we are seeking a motivated and driven consultant to become team member number 3. Offering an excellent work life balance, good working environment, table tennis table and an office dog (if that's what you look for)... but more importantly a blank canvass We are currently recruiting solely in Healthcare Communications, Medical Affairs and some Commercial roles, all other areas are untouched (no reputation smashes a poor one all day long). Looking for knowledge and expertise in: Regulatory Affairs / Quality Assurance Medical Devices Commercial Scientific / Laboratory Medical Affairs Clinical Research You will have: LinkedIn recruiter Job boards Freedom to meet clients and candidates Attendance to events where possible Free reign to build your own mini empire Globally recruiting freedom (US, ASIA, EUROPE) Excellent commission structure and a chance to really work SMART in a way. If you want to know more, drop me a note on LinkedIn, JAKE BYRNE or send your CV (let's face it, we all look at CV's enough to not bother sometimes with our own). Let's grab a beer and see what the future holds. Job Type: Full-time Salary: £18,000.00 to £60,000.00 /year 1 OTE
Hyper Recruitment Solutions Ltd
Cambridgeshire, UK
Hyper Recruitment Solutions are working with a Leading Regulatory Consultancy based in the Cambridgeshire area to identify an experience Client Manager to join them as their Regulatory Services Manager. In this position you will be responsible for customer satisfaction through ensuring project time lines and budgets are adhered to as well as through effective development of client relationships. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Regulatory Services Manager will be varied however the key duties and responsibilities are as follows: 1. Strategy - You will work with the company's leadership team to develop regulatory business strategy. You will focus on maximising revenues and ensure business processes are followed. You will ensure that team members are aware of changes to company strategy and provide strategic advise as required. 2. Operational - Ensure that processes are designed to help both technical experts and regulatory team members perform to the highest standard. You will be responsible for group Profit & Loss including budgeting and forecast and revenue claims. You will have the opportunity to suggest process improvements and will be able to contribute to design of projects. 3. Regulatory Project Lead - Manage workloads and resources to ensure revenue targets are met to maintain customer quality. Plan and monitor the progress of programmes to ensure time lines are achieved as well as managing performance initiatives (appraisals, grade/salary adjustments, disciplinary matters). 4. Customer Facing - Your aim will be to achieve high levels of customer satisfaction by ensuring all of the above is maintained. You will help promote the Regulatory Services Group by assisting sales teams and play an integral role in developing and maintaining client relationships including relationships with Regulatory agencies. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Regulatory Services Manager we are looking to identify the following on your profile and past history: 1. Relevant degree in a Life Sciences discipline or relevant industry experience. Ideally experience in a Scientific field would benefit your application. 2. Proven industry experience in of running a Regulatory Service is desirable but not essential. However experience with managing projects, ensuring time lines are maintained and managing resources and budgets is vital in your application 3. Experience of line managing staff including ensuring KPIs are achieved and develop staff members careers. Key Words: Regulatory Affairs | Consultant | Consultancy | Regulatory Services | Contract Manager | Client Management | Project Manager | Programme Management | Budgeting | Operations | Strategy | Line Management Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.
18/06/2019
Hyper Recruitment Solutions are working with a Leading Regulatory Consultancy based in the Cambridgeshire area to identify an experience Client Manager to join them as their Regulatory Services Manager. In this position you will be responsible for customer satisfaction through ensuring project time lines and budgets are adhered to as well as through effective development of client relationships. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Regulatory Services Manager will be varied however the key duties and responsibilities are as follows: 1. Strategy - You will work with the company's leadership team to develop regulatory business strategy. You will focus on maximising revenues and ensure business processes are followed. You will ensure that team members are aware of changes to company strategy and provide strategic advise as required. 2. Operational - Ensure that processes are designed to help both technical experts and regulatory team members perform to the highest standard. You will be responsible for group Profit & Loss including budgeting and forecast and revenue claims. You will have the opportunity to suggest process improvements and will be able to contribute to design of projects. 3. Regulatory Project Lead - Manage workloads and resources to ensure revenue targets are met to maintain customer quality. Plan and monitor the progress of programmes to ensure time lines are achieved as well as managing performance initiatives (appraisals, grade/salary adjustments, disciplinary matters). 4. Customer Facing - Your aim will be to achieve high levels of customer satisfaction by ensuring all of the above is maintained. You will help promote the Regulatory Services Group by assisting sales teams and play an integral role in developing and maintaining client relationships including relationships with Regulatory agencies. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Regulatory Services Manager we are looking to identify the following on your profile and past history: 1. Relevant degree in a Life Sciences discipline or relevant industry experience. Ideally experience in a Scientific field would benefit your application. 2. Proven industry experience in of running a Regulatory Service is desirable but not essential. However experience with managing projects, ensuring time lines are maintained and managing resources and budgets is vital in your application 3. Experience of line managing staff including ensuring KPIs are achieved and develop staff members careers. Key Words: Regulatory Affairs | Consultant | Consultancy | Regulatory Services | Contract Manager | Client Management | Project Manager | Programme Management | Budgeting | Operations | Strategy | Line Management Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.
HRM Senior Associate Our global pharmaceutical client based in Hoddesdon is recruiting a HRM Senior Associate to join their Regulatory team based in Hoddesdon. This is contract role is to start ASAP for approx. 6 months with a possible extension and the pay rate £20.00 to £34.25 per hour depending on experience. Position Overview : This role will be dealing with Brexit; Under the direction of the Health Registration Management (HRM) Regional Lead, the HRM Senior Associate you will be responsible for: Planning and executing updates to the HRM system in support of business operations relating to the United Kingdom leaving the European Union Ensuring the entry of accurate, complete and timely Regulatory Information into the HRM system Provide detailed updates at key milestones to ensure all activities are completed on time and within the project plan Education /Skills Bachelor's degree with 2 years of industry experience in a regulatory/compliance industry with emphasis on system support Required General global regulatory knowledge Knowledge of EU regulatory procedures e.g. MRP/DCP, CP Ability to follow instructions and work independently Broad organizational awareness and knowledge of touch points/interdependencies Demonstrated problem-solving skills Proven experience analysing information in support of data entry activities Excel, Word and PowerPoint Personal: Ability to be flexible within their daily work obligations Ability to communicate effectively at all levels Ability to work on their own initiative and within a team Ability to manage multiple tasks
18/06/2019
HRM Senior Associate Our global pharmaceutical client based in Hoddesdon is recruiting a HRM Senior Associate to join their Regulatory team based in Hoddesdon. This is contract role is to start ASAP for approx. 6 months with a possible extension and the pay rate £20.00 to £34.25 per hour depending on experience. Position Overview : This role will be dealing with Brexit; Under the direction of the Health Registration Management (HRM) Regional Lead, the HRM Senior Associate you will be responsible for: Planning and executing updates to the HRM system in support of business operations relating to the United Kingdom leaving the European Union Ensuring the entry of accurate, complete and timely Regulatory Information into the HRM system Provide detailed updates at key milestones to ensure all activities are completed on time and within the project plan Education /Skills Bachelor's degree with 2 years of industry experience in a regulatory/compliance industry with emphasis on system support Required General global regulatory knowledge Knowledge of EU regulatory procedures e.g. MRP/DCP, CP Ability to follow instructions and work independently Broad organizational awareness and knowledge of touch points/interdependencies Demonstrated problem-solving skills Proven experience analysing information in support of data entry activities Excel, Word and PowerPoint Personal: Ability to be flexible within their daily work obligations Ability to communicate effectively at all levels Ability to work on their own initiative and within a team Ability to manage multiple tasks
My client are a revolutionary tech company who are using Data Science and Machine learning to transform drug discovery. Currently, it takes 15 years and an average of $2.9bn to bring a drug to market- their software and quantum physics simulates that molecules and enables companies to make better informed decisions with drug development to ultimately improve patient outcomes. Their company is currently 15 people strong, they are a bright bunch- the majority of people having PhDs in related disciplines so you will be in amongst passionate and dedicated people. A recipe for success. You will be supported and nurtured and encouraged to maintain a positive work life balance whilst bringing your 'A game' and creative ideas to the table. They are looking for a DevOps Engineer to join their team, you will be tasked with setting up the infrastructure for the business using Python, Kubernetes, Docker, AWS. Working closely with the Data Scientists and Machine Learning Engineers you will be learning and picking up all sorts of data science knowledge and be given lots of opportunity for growth and learning. Competitive salary and benefits, get in touch if you would like to find out more about this exciting role.
18/06/2019
My client are a revolutionary tech company who are using Data Science and Machine learning to transform drug discovery. Currently, it takes 15 years and an average of $2.9bn to bring a drug to market- their software and quantum physics simulates that molecules and enables companies to make better informed decisions with drug development to ultimately improve patient outcomes. Their company is currently 15 people strong, they are a bright bunch- the majority of people having PhDs in related disciplines so you will be in amongst passionate and dedicated people. A recipe for success. You will be supported and nurtured and encouraged to maintain a positive work life balance whilst bringing your 'A game' and creative ideas to the table. They are looking for a DevOps Engineer to join their team, you will be tasked with setting up the infrastructure for the business using Python, Kubernetes, Docker, AWS. Working closely with the Data Scientists and Machine Learning Engineers you will be learning and picking up all sorts of data science knowledge and be given lots of opportunity for growth and learning. Competitive salary and benefits, get in touch if you would like to find out more about this exciting role.
Scantec Personnel
9 Stanley St, Liverpool L1 6AA, UK
QA Administrator - Document Control £25 - 28,000 plus 8% bonus, 10% pension, 36 days holiday Permanent Based in Liverpool Pharmaceutical industry An expanding multinational pharmaceutical company based in Liverpool are looking to appoint a QA Administrator to their team on a permanent basis. Details: The successful candidate will be responsible for the Document Control of documents on site across all functions including QA, Method Development, Manufacturing, Supply Chain and QC as they move to a new electronic based system. Working as part of a team of 3 within the wider QA group the successful QA Administrator will be helping to proof read new SOPs for new methods, managing the change control of GMP documentation, assisting in creating documentation for new projects and procedures. Qualifications and Experience: The role holder will ideally have QA experience of working with documentation systems within a pharmaceutical cGMP environment. Candidates from other heavily regulated industries i.e. Power Generation or Nuclear are also encouraged to apply Competent user of Microsoft Word and Excel. A Life Science Qualification is highly desirable e.g., HNC / HND minimum Good interpersonal, communication and team working skills are required. Good organisational skills with good attention to detail Time management, diplomacy, assertiveness, leadership and the ability to work under pressure are also essential. A positive, flexible and pro-active approach to work is required Keenness and ability to learn new skills. Good knowledge of IT systems. Ability to understand and work to written systems, and a methodical approach to performing duties. Helpful attitude, highly motivated team worker. For further details and to apply please contact Johnathan Miller at Scantec on 0151._ 666._ 8925 and johnathanm (at) scantec. co. uk Scantec Personnel Limited is acting as an employment business and an employment agency. For contract or interim roles (and unless otherwise stated), all pay rates stated are on a Limited Company basis. Due to the high volume of applications Scantec receives it is not always possible to acknowledge every application. Shortlisted applicants will be contacted within 28 days. If you don't hear from us within 28 days your application has not been shortlisted at this time, to be considered for future vacancies please register with us on our website.
18/06/2019
QA Administrator - Document Control £25 - 28,000 plus 8% bonus, 10% pension, 36 days holiday Permanent Based in Liverpool Pharmaceutical industry An expanding multinational pharmaceutical company based in Liverpool are looking to appoint a QA Administrator to their team on a permanent basis. Details: The successful candidate will be responsible for the Document Control of documents on site across all functions including QA, Method Development, Manufacturing, Supply Chain and QC as they move to a new electronic based system. Working as part of a team of 3 within the wider QA group the successful QA Administrator will be helping to proof read new SOPs for new methods, managing the change control of GMP documentation, assisting in creating documentation for new projects and procedures. Qualifications and Experience: The role holder will ideally have QA experience of working with documentation systems within a pharmaceutical cGMP environment. Candidates from other heavily regulated industries i.e. Power Generation or Nuclear are also encouraged to apply Competent user of Microsoft Word and Excel. A Life Science Qualification is highly desirable e.g., HNC / HND minimum Good interpersonal, communication and team working skills are required. Good organisational skills with good attention to detail Time management, diplomacy, assertiveness, leadership and the ability to work under pressure are also essential. A positive, flexible and pro-active approach to work is required Keenness and ability to learn new skills. Good knowledge of IT systems. Ability to understand and work to written systems, and a methodical approach to performing duties. Helpful attitude, highly motivated team worker. For further details and to apply please contact Johnathan Miller at Scantec on 0151._ 666._ 8925 and johnathanm (at) scantec. co. uk Scantec Personnel Limited is acting as an employment business and an employment agency. For contract or interim roles (and unless otherwise stated), all pay rates stated are on a Limited Company basis. Due to the high volume of applications Scantec receives it is not always possible to acknowledge every application. Shortlisted applicants will be contacted within 28 days. If you don't hear from us within 28 days your application has not been shortlisted at this time, to be considered for future vacancies please register with us on our website.
Technical Reviewer/Scientist - Analytical Services Role Purpose: A technical reviewer is required to support the flawless execution of scientific projects. They will be responsible for technically reviewing and signing off analytical data to a high-quality standard and in compliance with GMP principles in accordance with project timelines and internal delivery metrics. Key Accountabilities and Duties Performs technical review of assays for stability, evaluation, method transfer and characterisation studies against standard operating procedures, protocols and GMP principles. Communicates with operators, study directors and managers to close-out technical review of assays and provides feedback for the recognition / development of scientists and to train staff to reinforce best practice Interprets data against study specifications, identifies atypical results / trends within data and supports and leads discussions for process improvements Provides support for the progress of quality records such as atypical / out of specification investigations and deviations, and for department activities such as protocol / report writing and archiving The incumbent performs a variety of routine work within established policies and procedures and receives detailed instructions on new projects and assignments. Minimum Required Qualifications/Skills Education HND/BSc in relevant scientific discipline or relevant previous experience Preferred area of study: Biochemistry / Biotechnology Experience: Essential: Demonstrated experience / knowledge in a range of analytical methods Demonstrated experience / knowledge of reviewing data generated from analytical methods Desired: Experience of working in a contract research / laboratory environment Demonstrated knowledge of regulatory and GMP processes Skills: Good communication, organisation and prioritisation skills An ability to effectively plan and complete assigned tasks within the required timeframe Competent writing skills and proficient in the use of Microsoft Word and Excel Qualities & Attitude: Able to make quality decisions based on the best available scientific data Desire to learn and willing to impart knowledge Confident and resilient enough to thrive in a challenging environment Willing to undertake a range of tasks for the effective running of the department.
18/06/2019
Technical Reviewer/Scientist - Analytical Services Role Purpose: A technical reviewer is required to support the flawless execution of scientific projects. They will be responsible for technically reviewing and signing off analytical data to a high-quality standard and in compliance with GMP principles in accordance with project timelines and internal delivery metrics. Key Accountabilities and Duties Performs technical review of assays for stability, evaluation, method transfer and characterisation studies against standard operating procedures, protocols and GMP principles. Communicates with operators, study directors and managers to close-out technical review of assays and provides feedback for the recognition / development of scientists and to train staff to reinforce best practice Interprets data against study specifications, identifies atypical results / trends within data and supports and leads discussions for process improvements Provides support for the progress of quality records such as atypical / out of specification investigations and deviations, and for department activities such as protocol / report writing and archiving The incumbent performs a variety of routine work within established policies and procedures and receives detailed instructions on new projects and assignments. Minimum Required Qualifications/Skills Education HND/BSc in relevant scientific discipline or relevant previous experience Preferred area of study: Biochemistry / Biotechnology Experience: Essential: Demonstrated experience / knowledge in a range of analytical methods Demonstrated experience / knowledge of reviewing data generated from analytical methods Desired: Experience of working in a contract research / laboratory environment Demonstrated knowledge of regulatory and GMP processes Skills: Good communication, organisation and prioritisation skills An ability to effectively plan and complete assigned tasks within the required timeframe Competent writing skills and proficient in the use of Microsoft Word and Excel Qualities & Attitude: Able to make quality decisions based on the best available scientific data Desire to learn and willing to impart knowledge Confident and resilient enough to thrive in a challenging environment Willing to undertake a range of tasks for the effective running of the department.
Here is a new research role for an electrochemist looking for their next position at a materials science firm in the Oxford area. This Electrochemist role is ideal for a PhD graduate looking for a new product development. The successful appointment will enjoy excellent career progression potential as an integral team member as the company transitions to full launch. Your day to day duties as an Electrochemist will be: Managing your own R&D projects, from the lab through to external site trials Liaison across the business, particularly with field engineers as they launch product on customer sites Development of novel formulations and testing methods You will be an ideal candidate with this background: A degree (or higher) in chemistry or similar Electrochemistry knowledge General curiosity to develop brand new offerings in the marketplace A track record in material or chemical product development A good team-working approach This client is currently shortlisting for the role so please apply immediately with a CV (Word document format, 2 pages maximum). Note my client is unable to sponsor visas for those without eligibility to work in the UK. Why should you work with Dr Paul Mears as your scientific specialist recruiter at Science Solutions? I focus solely on matching scientists to positions in the UK speciality chemical industry, which is where my own experience and network position me best given a background working in the speciality chemicals and fragrance and flavours sectors. I completed academic studies with a PhD in organic chemistry at the University of Manchester, which followed a BSc in the University of Leeds' famous Colour & Polymer Chemistry department. Following a short post-doctoral research post I built up three years' experience in recruiting scientists into new jobs. Full references and testimonials of successful assignments such as Technical Directors, Heads of Operations and quick turnarounds for urgent laboratory needs can be found on my LinkedIn profile - search Paul Mears.
18/06/2019
Here is a new research role for an electrochemist looking for their next position at a materials science firm in the Oxford area. This Electrochemist role is ideal for a PhD graduate looking for a new product development. The successful appointment will enjoy excellent career progression potential as an integral team member as the company transitions to full launch. Your day to day duties as an Electrochemist will be: Managing your own R&D projects, from the lab through to external site trials Liaison across the business, particularly with field engineers as they launch product on customer sites Development of novel formulations and testing methods You will be an ideal candidate with this background: A degree (or higher) in chemistry or similar Electrochemistry knowledge General curiosity to develop brand new offerings in the marketplace A track record in material or chemical product development A good team-working approach This client is currently shortlisting for the role so please apply immediately with a CV (Word document format, 2 pages maximum). Note my client is unable to sponsor visas for those without eligibility to work in the UK. Why should you work with Dr Paul Mears as your scientific specialist recruiter at Science Solutions? I focus solely on matching scientists to positions in the UK speciality chemical industry, which is where my own experience and network position me best given a background working in the speciality chemicals and fragrance and flavours sectors. I completed academic studies with a PhD in organic chemistry at the University of Manchester, which followed a BSc in the University of Leeds' famous Colour & Polymer Chemistry department. Following a short post-doctoral research post I built up three years' experience in recruiting scientists into new jobs. Full references and testimonials of successful assignments such as Technical Directors, Heads of Operations and quick turnarounds for urgent laboratory needs can be found on my LinkedIn profile - search Paul Mears.
