Unfortunately, we are unable to offer visa sponsorship for this role.
This is a full time, permanent position working a flexible 36.5 hour week, Monday – Friday.
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 coordinate sample analysis activities, support stability studies conducted at CROs, and generate high‑quality reports that meet regulatory, scientific, and client standards.
- 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.