Method Validation - 27+ job offers

Role Overview We are seeking a Responsible Scientist to lead LC-MS/MS bioanalytical studies, ensuring scientific integrity, regulatory compliance, and successful study delivery. Key Responsibilities Act as scientific lead for LC-MS/MS bioanalytical studies conducted under GLP and GCP Oversee method

Role Overview We are seeking a Principal Scientist to act as a subject matter expert across LC-MS/MS bioanalytical programmes supporting PK and PD studies. This role provides scientific leadership across multiple studies, focusing on complex problem-solving, assay strategy, and client engagement. Ke

Job title: Analytical Scientist Location: Hamble, United Kingdom Department: Global Technical Innovation Group (GTIG) Working Hours - Mon-Fri, 37.5 hours per week A brighter future awaits you. CooperVision is one of the world’s leading manufacturers of soft contact lenses with a presence in over 100

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life scie

Associate Principal Scientist – Analytical Project Lead Macclesfield, UK About AstraZeneca Join the team where everyone feels a personal connection to the people that we impact. From our science labs to manufacturing at scale, we are committed to delivering at the highest quality. It’s inspiring and

*This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.** *Work Schedule** Standard (Mon-Fri) *Environmental Conditions** Adherence to all Good Manufacturi

A leading pharmaceutical company in Scotland seeks an Analytical Development Scientist to support method development, validation, and technical transfer in a GMP-compliant setting. You will lead and manage analytical projects that impact quality and compliance, working cross-functionally with teams

A leading life sciences company is seeking a QC Associate for their Bristol, PA location. The role involves critical technical review, method qualification, and execution of laboratory testing for GMP manufacturing. The ideal candidate has a strong background in GMP analytical testing, a scientific

A leading analytical testing services provider in Livingston, UK, is seeking a candidate to support the Chemistry department. Responsibilities include conducting chemistry testing, overseeing method validation, and client communications. Candidates should have a solid understanding of GMP and releva

A well-established pharmaceutical organisation in the North East is seeking a Method Validation Chemist. You will develop, validate, and transfer analytical methods while ensuring compliance with GMP standards. The ideal candidate has a degree in Chemistry or Pharmaceutical Science and experience in

Method Validation Chemist As a Method Validation Chemist, you will be responsible for developing, validating and transferring analytical methods used to support pharmaceutical products and raw materials. Working within a GMP-regulated laboratory, you will play a key role in ensuring analytical metho

Job Description Do you have the right skills and experience for this role Read on to find out, and make your application. Analytical Development Scientist Location: Huddersfield Rate: £18.91 per hour Contract Length: 6 Months Role Purpose Provide measurement science to generate and improve manufactu

ABOUT YOU This role is ideal for an experienced scientist with a strong foundation in biophysics and large-molecule analysis, who enjoys working independently, applying technical expertise to complex analytical challenges, and collaborating closely with colleagues and clients. You will bring strong

Method Validation Chemist As a Method Validation Chemist , you will be responsible for developing, validating and transferring analytical methods used to support pharmaceutical products and raw materials. Working within a GMP-regulated laboratory, you will play a key role in ensuring analytical meth

Introduction to role: Are you ready to lead API analytics that accelerate novel oncology medicines from concept to candidate selection and ultimately to reach patients? Do you thrive at the interface of LC-MS science, digital enablement, and cross-functional decision-making to unlock clearer, faster

Join a business on an impressive trajectory of growth Great routes forward for progression About Our Client Our client is an established Pharmaceutical Manufacturer with an impressive on site R&D facility Job Description Manage and execute method validation activities in alignment with regulatory re

Method Validation Chemist As a Method Validation Chemist , you will be responsible for developing, validating and transferring analytical methods used to support pharmaceutical products and raw materials. Working within a GMP-regulated laboratory, you will play a key role in ensuring analytical meth

Quality Control Lead Application Deadline: 31 May 2026 Department: Quality Employment Type: Full Time Location: Newmarket, Suffolk Reporting To: QHSE Manager Description Wychem, an Ascensus Specialties Company, is seeking a Quality Control (QC) Lead to join our operations team. Reporting directly to

We Are Rosemont For over 50 years, Rosemont Pharmaceuticals has been a trusted name in the development and manufacture of oral liquid medicines. With a portfolio of over 130 products — including 70 licensed medicines — we’re proud to support healthcare professionals and patients, especially those wi

Company Overview At Labcorp, we believe in the power of science to change lives. We are nearly 70,000 people across 100 countries who are harnessing science for human good. Our work combines unparalleled diagnostic laboratories, drug development capabilities and commercial innovations. Together, we