Continuous Improvement jobs in United Kingdom

Pharmidex is pleased to offer an opportunity for a Bioanalytical Scientist with strong regulatory study experience to join our Bioanalytical team. This role is suited to an experienced scientist who enjoys hands‑on laboratory work and delivering bioanalytical data for GLP and GCP-regulated studies.

You will support the execution of regulated bioanalytical studies from method development through to reporting, working closely with internal teams and, where appropriate, external clients.

• Perform LC‑MS bioanalysis in support of GLP/GCP-regulated studies
• Conduct method development, validation, and sample analysis
• Execute regulated study work in accordance with SOPs and QA expectations
• Prepare and review analytical data for study reports
• Maintain accurate documentation and laboratory records
• Support client interactions, data interpretation, and study discussions (dependent on experience)

• Degree in Chemistry or a closely related discipline
• ≥5 years’ experience in a bioanalytical laboratory environment
• Demonstrable experience supporting regulatory (GLP and/or GCP) studies
• Strong hands‑on experience with:
• Liquid chromatography and mass spectrometry
• Large molecule and peptide bioanalysis
• Experience in oligonucleotide bioanalysis
• Strong communication skills and ability to work within multidisciplinary teams
• Experience acting as Study Director or Principal Investigator for bioanalytical studies
• Prior client‑facing responsibilities
• Knowledge of ADMET and drug discovery workflows
• Experience working within a CRO environment
• Exposure to biotherapeutics

Joining Pharmidex means becoming part of a high-performing CRO supporting regulated and non-regulated programmes for global clients. We value quality, accountability, and scientific excellence.

Please send your CV and a short cover note to Careers@Pharmidex.com