Job Description This is a fulltime, permanent position, working a flexible 36.5 hour week, Monday – Friday. The purpose of this job is to support analysis of pharmaceutical Oral Drug Products and New Modalities with accurate results within an acceptable timeframe. Job Responsibilities: To perform routine and non-routine analysis using traditional and modern analytical techniques, as required by the Lead Scientist or customer representative. Experience in chromatography and ideally using Empower CDS and able to carry out technical reviews. Ability to coordinate sample analysis, support stability studies at CROs and generate reports. Ideally, experience working with Peptide molecules would be highly valued. To review analytical data for GMP compliance. In line with experience, support development and validation of analytical procedures used for Oral Drug Products and New Modalities. To prepare and approve results for tests in which they have received the appropriate training and are deemed competent. To train as required, other Eurofins or client employees in analytical techniques and electronic system in which the Analyst is competent. To initiate and follow-up OOS results and action limits as per customer procedures. To identify any opportunities for improvement of quality and service and work with the team to implement continuous improvement. To document data as dictated by current client policies and procedures. To ensure that all documentation is carried out on time, is accurate and legible and conforms to the relevant quality standards. To update any relevant documentation when requested by Lead Scientist or client representative. To participate in the preparation of reportss