Job Opportunity: Senior LCMS Scientist Salary : 30,000 - 38,000 Location : Cheshire, UK Type : Permanent Overview Join our team as a Senior LCMS Scientist, making key contributions to pharmaceutical product development through analytical excellence using Liquid Chromatography-Mass Spectrometry (LCMS). Key Responsibilities Lead LCMS activities across drug development stages. Develop, optimize, and validate LCMS methods. Resolve complex LCMS challenges. Collaborate with multidisciplinary teams to achieve project goals. Ensure compliance with regulatory standards for method validation. Analyze LCMS data, create reports, and present findings. Innovate and improve LCMS methodologies. Qualifications Degree (BSc, MSc, PhD) in Analytical Chemistry, Chemistry, or related field. Extensive LCMS experience, preferably in pharmaceutical analysis. Proven expertise in developing and troubleshooting LCMS methods for APIs and raw materials. Strong communication skills to convey complex data effectively. Proficiency with software like Empower or UNIFI (advantageous). Benefits Salary: 30,000 - 38,000 Company pension scheme Health and life insurance Apply Now Note : Applicants must have the right to work in the UK. Visa sponsorship not available. We are an Equal Opportunities Employer committed to fostering inclusivity.
Nov 10, 2026
Full time
Job Opportunity: Senior LCMS Scientist Salary : 30,000 - 38,000 Location : Cheshire, UK Type : Permanent Overview Join our team as a Senior LCMS Scientist, making key contributions to pharmaceutical product development through analytical excellence using Liquid Chromatography-Mass Spectrometry (LCMS). Key Responsibilities Lead LCMS activities across drug development stages. Develop, optimize, and validate LCMS methods. Resolve complex LCMS challenges. Collaborate with multidisciplinary teams to achieve project goals. Ensure compliance with regulatory standards for method validation. Analyze LCMS data, create reports, and present findings. Innovate and improve LCMS methodologies. Qualifications Degree (BSc, MSc, PhD) in Analytical Chemistry, Chemistry, or related field. Extensive LCMS experience, preferably in pharmaceutical analysis. Proven expertise in developing and troubleshooting LCMS methods for APIs and raw materials. Strong communication skills to convey complex data effectively. Proficiency with software like Empower or UNIFI (advantageous). Benefits Salary: 30,000 - 38,000 Company pension scheme Health and life insurance Apply Now Note : Applicants must have the right to work in the UK. Visa sponsorship not available. We are an Equal Opportunities Employer committed to fostering inclusivity.
Principal Scientist - Analytical Overview A global pharmaceutical organisation are seeking a Principal Scientist to join their analytical development team in a state-of-the-art facility supporting cutting-edge API development. This is an excellent opportunity for an individual looking to advance their career in analytical chemistry with broad responsibilties across AD, project management and commercial activites. Responsibilities Collaborate with cross-functional teams to support drug substance process research and development. Develop and implement innovative analytical strategies to enhance operational efficiency and deliver high-quality results. Ensure compliance with industry standards, regulations, and company policies specific to analytical methodologies and practices. Provide scientific leadership and mentorship to team members, fostering a culture of technical excellence and continuous learning. Analyse complex datasets and generate comprehensive reports to support decision-making processes. Identify opportunities for growth, innovation, and process improvement within the analytical sciences space. Qualifications Proven experience as a Principal Scientist or in a similar scientific role, demonstrating a strong track record of success in analytical sciences. Strong expertise in analytical techniques, problem-solving, and method development. Excellent communication, leadership, and collaboration skills. Ability to independently manage complex projects and collaborate effectively with multidisciplinary teams. Proficiency in advanced analytical tools and relevant software. A degree (PhD preferred) in chemistry, biochemistry, analytical sciences, or a related field is required. Benefits Competitive salary of up to 57K. Opportunities for professional development and career progression in advanced analytical sciences. A supportive and inclusive work environment that values innovation and excellence. Access to a state-of-the-art facility equipped with the latest technology to facilitate your work. Comprehensive benefits package, including pension contributions and health coverage. Flexible working arrangements to promote work-life balance. If you are an experienced and results-driven professional specialising in analytical sciences, we encourage you to apply for this exciting opportunity. Join us to contribute your expertise, work in a modern research environment, and take the next significant step in your career.
Nov 10, 2026
Full time
Principal Scientist - Analytical Overview A global pharmaceutical organisation are seeking a Principal Scientist to join their analytical development team in a state-of-the-art facility supporting cutting-edge API development. This is an excellent opportunity for an individual looking to advance their career in analytical chemistry with broad responsibilties across AD, project management and commercial activites. Responsibilities Collaborate with cross-functional teams to support drug substance process research and development. Develop and implement innovative analytical strategies to enhance operational efficiency and deliver high-quality results. Ensure compliance with industry standards, regulations, and company policies specific to analytical methodologies and practices. Provide scientific leadership and mentorship to team members, fostering a culture of technical excellence and continuous learning. Analyse complex datasets and generate comprehensive reports to support decision-making processes. Identify opportunities for growth, innovation, and process improvement within the analytical sciences space. Qualifications Proven experience as a Principal Scientist or in a similar scientific role, demonstrating a strong track record of success in analytical sciences. Strong expertise in analytical techniques, problem-solving, and method development. Excellent communication, leadership, and collaboration skills. Ability to independently manage complex projects and collaborate effectively with multidisciplinary teams. Proficiency in advanced analytical tools and relevant software. A degree (PhD preferred) in chemistry, biochemistry, analytical sciences, or a related field is required. Benefits Competitive salary of up to 57K. Opportunities for professional development and career progression in advanced analytical sciences. A supportive and inclusive work environment that values innovation and excellence. Access to a state-of-the-art facility equipped with the latest technology to facilitate your work. Comprehensive benefits package, including pension contributions and health coverage. Flexible working arrangements to promote work-life balance. If you are an experienced and results-driven professional specialising in analytical sciences, we encourage you to apply for this exciting opportunity. Join us to contribute your expertise, work in a modern research environment, and take the next significant step in your career.
Job Advertisement: Senior QC Analyst (6-Month FTC Contract Role) Overview Salary 30,000 - 35,000 pro rata We are seeking a highly skilled and experienced Senior QC Analyst for a 6-month fixed-term contract to join a pharmaceutical manufacturing organisation. Reporting directly to the QC Manager, this role is integral to ensuring the quality and compliance of pharmaceutical products. If you are a detail-oriented professional with a strong background in Quality Control and a passion for excellence, we encourage you to apply. Responsibilities As a Senior QC Analyst, your key responsibilities will include: Supervising and leading a team of analysts in the Quality Control laboratory, ensuring compliance with Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP). Reviewing Batch Manufacturing Documents and analytical test results to facilitate product release. Performing analytical testing of manufactured product samples for release, stability studies, and validation using techniques such as HPLC and GC. Assigning duties to analysts based on production release requirements, ensuring efficient laboratory operations. Reviewing and approving product labels for use by the Production Department. Preparing and reviewing Standard Operating Procedures, Raw Material Documents, Analytical Test Reports, Validation Protocols, and Reports. Providing technical support, troubleshooting analytical methods, and maintaining laboratory equipment. Ensuring laboratory housekeeping is maintained to appropriate standards. Supporting inspection readiness and promoting a culture of continuous improvement. Collaborating with Quality Assurance and Production teams to ensure seamless operations. Reviewing analytical data against pharmacopeial and registered specifications. Qualifications To be successful in this role, you will need: A degree in Chemical Sciences or equivalent practical experience. A minimum of 5 years of Quality Control/Analytical experience within a GMP environment. Proficiency in analytical techniques, including IR and NIR spectroscopy, High-Performance Liquid Chromatography (HPLC), and Gas Chromatography (GC). Strong analytical thinking, problem-solving, and troubleshooting skills. Excellent communication skills, both verbal and written, with a keen eye for detail. Good computer literacy and familiarity with laboratory systems. A commitment to health and safety practices, including ensuring team members are adequately trained in safety protocols and the use of PPE. Benefits Competitive compensation for the duration of the 6-month fixed-term contract. Opportunity to work in a dynamic and well-established pharmaceutical manufacturing environment. Gain valuable experience in a leadership role within a Quality Control function. Contribute to the production of high-quality pharmaceutical products that make a difference in people's lives. If you are ready to take on this exciting 6-month fixed-term opportunity and bring your expertise to our team, we look forward to receiving your application. Note: No sponsorship is available for this position
Nov 10, 2026
Full time
Job Advertisement: Senior QC Analyst (6-Month FTC Contract Role) Overview Salary 30,000 - 35,000 pro rata We are seeking a highly skilled and experienced Senior QC Analyst for a 6-month fixed-term contract to join a pharmaceutical manufacturing organisation. Reporting directly to the QC Manager, this role is integral to ensuring the quality and compliance of pharmaceutical products. If you are a detail-oriented professional with a strong background in Quality Control and a passion for excellence, we encourage you to apply. Responsibilities As a Senior QC Analyst, your key responsibilities will include: Supervising and leading a team of analysts in the Quality Control laboratory, ensuring compliance with Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP). Reviewing Batch Manufacturing Documents and analytical test results to facilitate product release. Performing analytical testing of manufactured product samples for release, stability studies, and validation using techniques such as HPLC and GC. Assigning duties to analysts based on production release requirements, ensuring efficient laboratory operations. Reviewing and approving product labels for use by the Production Department. Preparing and reviewing Standard Operating Procedures, Raw Material Documents, Analytical Test Reports, Validation Protocols, and Reports. Providing technical support, troubleshooting analytical methods, and maintaining laboratory equipment. Ensuring laboratory housekeeping is maintained to appropriate standards. Supporting inspection readiness and promoting a culture of continuous improvement. Collaborating with Quality Assurance and Production teams to ensure seamless operations. Reviewing analytical data against pharmacopeial and registered specifications. Qualifications To be successful in this role, you will need: A degree in Chemical Sciences or equivalent practical experience. A minimum of 5 years of Quality Control/Analytical experience within a GMP environment. Proficiency in analytical techniques, including IR and NIR spectroscopy, High-Performance Liquid Chromatography (HPLC), and Gas Chromatography (GC). Strong analytical thinking, problem-solving, and troubleshooting skills. Excellent communication skills, both verbal and written, with a keen eye for detail. Good computer literacy and familiarity with laboratory systems. A commitment to health and safety practices, including ensuring team members are adequately trained in safety protocols and the use of PPE. Benefits Competitive compensation for the duration of the 6-month fixed-term contract. Opportunity to work in a dynamic and well-established pharmaceutical manufacturing environment. Gain valuable experience in a leadership role within a Quality Control function. Contribute to the production of high-quality pharmaceutical products that make a difference in people's lives. If you are ready to take on this exciting 6-month fixed-term opportunity and bring your expertise to our team, we look forward to receiving your application. Note: No sponsorship is available for this position
