Biophysical Characterisation Analyst Annual Salary: 32k - 36k DOE Location: Greater Manchester Job Type: Permanent, Full Time Reed Scientific is excited to announce an opportunity for a Biophysical Characterisation Analyst to join our client's GMP/GLP laboratories. Due to year-on-year success and business growth, we are seeking experienced scientists who are proficient in techniques such as c-IEF, CE-SDS, SDS-PAGE, mRNA analysis techniques, and ELISA/Plate based residual impurity analysis, primarily for the analysis of Biopharmaceutical products. Day-to-day of the role: Support a wide array of projects involving routine analysis, method development, method validations, and troubleshooting across varying scales, scopes, and timelines. Plan and perform analytical work, generating and interpreting data, and writing reports when required. Liaise proactively and reactively with others inside and outside the department to provide or obtain information, ensuring effective completion of work. Build relationships and contacts to facilitate future exchange of information. Required Skills & Qualifications: BSc / MSc/ PhD in Biochemistry/Chemistry or a related scientific discipline is essential. In-depth knowledge of Biological Characterisation with extensive experience using Biophysical and Chromatography techniques for the analysis of biopharmaceuticals, such as UV, CD, NMR, FTIR, fluorescence, SEC-MALS, AUC, DLS, and DSC. Comprehensive experience working in a GxP regulatory laboratory with a strong understanding of GLP/GMP principles. Strong method development and validation experience. Experience working with large molecules and proteins. Experience in Oligonucleotide & mRNA analysis would be very advantageous. Demonstrable experience in training, supervising, and coordinating the work of more junior scientists. Good practical laboratory and problem-solving skills. Good IT literacy skills. Clear written and verbal communication skills with the ability to clearly convey processes, results, and key messages and able to build rapport quickly and effectively. Benefits: Competitive salary and benefits package. Opportunities for professional growth and development. Supportive team environment. How to Apply: If you are interested in the Biophysical Characterisation Analyst role and meet the qualifications, please submit your CV detailing your relevant experience and why you are interested in this position. We regret to inform that we cannot provide sponsorship to work in the UK.
May 22, 2026
Full time
Biophysical Characterisation Analyst Annual Salary: 32k - 36k DOE Location: Greater Manchester Job Type: Permanent, Full Time Reed Scientific is excited to announce an opportunity for a Biophysical Characterisation Analyst to join our client's GMP/GLP laboratories. Due to year-on-year success and business growth, we are seeking experienced scientists who are proficient in techniques such as c-IEF, CE-SDS, SDS-PAGE, mRNA analysis techniques, and ELISA/Plate based residual impurity analysis, primarily for the analysis of Biopharmaceutical products. Day-to-day of the role: Support a wide array of projects involving routine analysis, method development, method validations, and troubleshooting across varying scales, scopes, and timelines. Plan and perform analytical work, generating and interpreting data, and writing reports when required. Liaise proactively and reactively with others inside and outside the department to provide or obtain information, ensuring effective completion of work. Build relationships and contacts to facilitate future exchange of information. Required Skills & Qualifications: BSc / MSc/ PhD in Biochemistry/Chemistry or a related scientific discipline is essential. In-depth knowledge of Biological Characterisation with extensive experience using Biophysical and Chromatography techniques for the analysis of biopharmaceuticals, such as UV, CD, NMR, FTIR, fluorescence, SEC-MALS, AUC, DLS, and DSC. Comprehensive experience working in a GxP regulatory laboratory with a strong understanding of GLP/GMP principles. Strong method development and validation experience. Experience working with large molecules and proteins. Experience in Oligonucleotide & mRNA analysis would be very advantageous. Demonstrable experience in training, supervising, and coordinating the work of more junior scientists. Good practical laboratory and problem-solving skills. Good IT literacy skills. Clear written and verbal communication skills with the ability to clearly convey processes, results, and key messages and able to build rapport quickly and effectively. Benefits: Competitive salary and benefits package. Opportunities for professional growth and development. Supportive team environment. How to Apply: If you are interested in the Biophysical Characterisation Analyst role and meet the qualifications, please submit your CV detailing your relevant experience and why you are interested in this position. We regret to inform that we cannot provide sponsorship to work in the UK.
Product Development Scientist Working Hours: Monday to Friday (8:00am - 4:00pm) Salary: 30,000 - 32,000 + 5% bonus Benefits: Private Healthcare 25 days annual leave, with the option to buy or sell up to 5 additional days Income Protection Insurance Life Assurance Pension scheme with employer contributions up to 12% Benefits platform Job Scope As part of assigned projects, the Product Development Scientist will contribute to the development of new In Vitro Diagnostics (IVD) products and/or the improvement of existing technologies. This role spans the full product lifecycle, from feasibility through to launch, ensuring compliance with design requirements and quality system procedures. Key Responsibilities Participate in all stages of the product development process, following direction from the Team Manager Provide regular updates to the Team Manager and Technical Experts on project progress, including technical performance and timelines Ensure accurate completion and availability of documentation related to assigned activities Support technical investigations into complaints and non-conforming performance trends Contribute to the evaluation and testing of new raw materials and technological innovations Troubleshoot issues associated with existing products Assist in developing process design specifications and conduct studies to confirm processes meet defined requirements Analyse and interpret experimental data, preparing clear and concise reports Carry out project activities in accordance with applicable regulations, SOPs, and quality standards Prepare and support GMP manufacturing campaigns in line with project timelines Respond to technical queries as needed Work closely with Health & Safety and Operations teams to ensure COSHH and risk assessments are completed for new product scale-up Experience, Knowledge & Skills Degree (Honours) in Biology, Chemistry, Biochemistry, Biomedical Science, Biomolecular Science, or a related life sciences discipline (essential) Previous laboratory experience is advantageous but not essential Strong communication and interpersonal skills Flexible and adaptable approach to work Ability to work both independently and collaboratively within a team Proficient IT skills, particularly in Microsoft Office Apply now to be considered for this opportunity. Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website.
May 22, 2026
Full time
Product Development Scientist Working Hours: Monday to Friday (8:00am - 4:00pm) Salary: 30,000 - 32,000 + 5% bonus Benefits: Private Healthcare 25 days annual leave, with the option to buy or sell up to 5 additional days Income Protection Insurance Life Assurance Pension scheme with employer contributions up to 12% Benefits platform Job Scope As part of assigned projects, the Product Development Scientist will contribute to the development of new In Vitro Diagnostics (IVD) products and/or the improvement of existing technologies. This role spans the full product lifecycle, from feasibility through to launch, ensuring compliance with design requirements and quality system procedures. Key Responsibilities Participate in all stages of the product development process, following direction from the Team Manager Provide regular updates to the Team Manager and Technical Experts on project progress, including technical performance and timelines Ensure accurate completion and availability of documentation related to assigned activities Support technical investigations into complaints and non-conforming performance trends Contribute to the evaluation and testing of new raw materials and technological innovations Troubleshoot issues associated with existing products Assist in developing process design specifications and conduct studies to confirm processes meet defined requirements Analyse and interpret experimental data, preparing clear and concise reports Carry out project activities in accordance with applicable regulations, SOPs, and quality standards Prepare and support GMP manufacturing campaigns in line with project timelines Respond to technical queries as needed Work closely with Health & Safety and Operations teams to ensure COSHH and risk assessments are completed for new product scale-up Experience, Knowledge & Skills Degree (Honours) in Biology, Chemistry, Biochemistry, Biomedical Science, Biomolecular Science, or a related life sciences discipline (essential) Previous laboratory experience is advantageous but not essential Strong communication and interpersonal skills Flexible and adaptable approach to work Ability to work both independently and collaboratively within a team Proficient IT skills, particularly in Microsoft Office Apply now to be considered for this opportunity. Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website.
Walker Cole International is searching for a Senior R&D Scientist - E&L and Nitrosamine Method Development - to join a global pharmaceutical company at their R&D and GMP-regulated site in the UK. As the Senior Scientist, you will play a key role in developing and validating analytical methods to support Extractables, Leachables, and Nitrosamine testing across pharmaceutical products and materials. Your responsibilities will include: Leading and supporting risk assessments and analytical method development for E&L and Nitrosamines. Developing, validating, and transferring LC-MS and GC-MS methods in compliance with GMP and regulatory guidelines. Performing data interpretation, troubleshooting, and technical investigations to resolve analytical issues. Preparing technical reports and regulatory documentation to support product filings and submissions. Collaborating with QC, QA, and Regulatory Affairs teams to ensure analytical compliance and product quality. Contributing to continuous improvement within analytical R&D and supporting method optimisation projects. To be successful, you will have: Proven experience in Extractables & Leachables and/or Nitrosamine analysis within a GMP-regulated laboratory. Hands-on experience with LC-MS or GC-MS and method validation techniques. Strong problem-solving, communication, and documentation skills. Analytical Chemistry Extractables & Leachables Nitrosamines LC-MS GC-MS Method Development Validation GMP Pharmaceuticals R&D
Oct 06, 2025
Full time
Walker Cole International is searching for a Senior R&D Scientist - E&L and Nitrosamine Method Development - to join a global pharmaceutical company at their R&D and GMP-regulated site in the UK. As the Senior Scientist, you will play a key role in developing and validating analytical methods to support Extractables, Leachables, and Nitrosamine testing across pharmaceutical products and materials. Your responsibilities will include: Leading and supporting risk assessments and analytical method development for E&L and Nitrosamines. Developing, validating, and transferring LC-MS and GC-MS methods in compliance with GMP and regulatory guidelines. Performing data interpretation, troubleshooting, and technical investigations to resolve analytical issues. Preparing technical reports and regulatory documentation to support product filings and submissions. Collaborating with QC, QA, and Regulatory Affairs teams to ensure analytical compliance and product quality. Contributing to continuous improvement within analytical R&D and supporting method optimisation projects. To be successful, you will have: Proven experience in Extractables & Leachables and/or Nitrosamine analysis within a GMP-regulated laboratory. Hands-on experience with LC-MS or GC-MS and method validation techniques. Strong problem-solving, communication, and documentation skills. Analytical Chemistry Extractables & Leachables Nitrosamines LC-MS GC-MS Method Development Validation GMP Pharmaceuticals R&D
