*Join an Innovative GLP Clinical Study Analytical Team*
Summary: Lead analytical staff, bioanalysis, and laboratory management to achieve project milestones, maintaining audit-readiness in state-of-the-art laboratories.
Key Responsibilities:
* Perform and oversee drug extraction from biological matrices using established analytical methods for PK and residue analysis.
* Supervise and train analysts, ensuring accuracy, precision, and adherence to quality standards.
* Conduct laboratory investigations and root cause analysis, implementing CAPA to drive continuous improvement.
* Oversee validation, maintenance, and troubleshooting of lab equipment, including HPLC and UPLC systems.
* Prepare and review SOPs and Analytical Reports, upholding the highest standards of GLP compliance and safety.
About You:
* Degree in Biochemistry, Chemistry, Biology, or a related scientific field.
* 3+ years' experience with U/HPLC in a GXP/GLP/GMP lab environment.
* 2+ years' experience in training and supervising lab analysts.
* Proficiency in Solvent and Solid Phase Extractions (SPE) of drug actives from biological matrices.
* Skilled in root cause analysis and CAPA implementation.
Desirable Skills:
* Experience with LCMS/MS in a GXP lab setting.
* Familiarity with HPLC/UPLC troubleshooting and lab documentation management.
* Proactive approach to lab efficiency improvements and supporting new staff onboarding.
What's in It for You:
* Competitive salary (DOE)
* Subsidised canteen
* Car insurance discount
* 32 days of annual leave
* Life assurance
* Company pension scheme
* Healthcare cash plan
* Professional development and growth opportunities
* Free on-site parking