Analytical Product Development Scientist

Analytical Product Development Scientist

Eurofins

Macclesfield, United Kingdom

As an Analytical Product Development Scientist you will support in the analysis of pharmaceutical Oral Drug Products and New Modalities with accurate results within an acceptable timeframe.

Job Responsibilities that you be covering

• As an Analytical Product Development Scientist, you will perform routine and non‑routine analysis using both traditional and modern analytical techniques and ensure all work is completed in line with GMP expectations and project requirements.
• You will apply your experience in chromatography, ideally including the use of Empower CDS, to conduct analytical testing and technical reviews, ensuring data accuracy, compliance, and scientific integrity throughout the development lifecycle.
• You will contribute to the development and validation of analytical procedures used for oral drug products and emerging new modalities,
• You will prepare and approve analytical results for tests in which you are trained and deemed competent, and you will support the training of Eurofins or client employees in analytical techniques and electronic systems where you hold demonstrable expertise.
• You will review analytical data for GMP compliance and initiate or follow up on OOS results and action limits when required.

Qualifications

• What skills, qualifications and experiences you will hold as an Analytical Product Development Scientist
• To succeed in this role, you will have a degree in Chemistry or a related discipline, supported by proven experience in pharmaceutical analysis within a development laboratory or equivalent environment.
• You will be experienced and competent in the use of traditional analytical techniques and modern instrumental methods, including HPLC, Karl Fischer, Dissolution, Mass Spectroscopy, and other spectroscopic techniques, with the ability to interpret raw data and troubleshoot analytical methods and instrumentation.
• You will have a thorough understanding of chromatographic techniques, including troubleshooting capabilities that support method robustness, data integrity, and scientific reliability.
• You will have a strong understanding of GMP expectations and their application in day‑to‑day laboratory operations, ensuring all analytical work meets regulatory and quality standards.
• You will be able to learn new processes quickly, work proactively to improve existing workflows, and contribute ideas that support continuous improvement in analytical development and laboratory efficiency.