The role involves coordinating day-to-day In-Process laboratory activities to meet turnaround times for critical real-time analysis across solvent recovery and drug-product operations
Job Summary
The role involves coordinating day-to-day In-Process laboratory activities to meet turnaround times for critical real-time analysis across solvent recovery and drug-product operations.
Candidates must ensure all testing activities comply with cGMP, DI requirements, site QMS, and safety/environmental rules while managing electronic data and documentation.
The position serves as the main auditee for internal and external regulatory inspections and supports the development of innovative treatments for Hepatitis C, HIV, and immuno-oncology.
Matching Summary
The role involves coordinating day-to-day In-Process laboratory activities to meet turnaround times for critical real-time analysis across solvent recovery and drug-product operations.
Skills & Requirements
Must-have
Minimum BSc in Chemistry or Life Sciences
Solid analytical laboratory experience in cGMP
Strong knowledge of GMP quality systems
Hands-on experience with LIMS Empower Tiamo
Excellent organization planning and time-management
Nice-to-have
Experience leading investigations and implementing CAPAs
Ability to work cross-functionally and deputise
Demonstrated problem-solving and continuous improvement skills
Key Requirements
Minimum BSc in Chemistry or related Life Sciences discipline
Solid analytical laboratory experience in a cGMP environment
Competence with Word Excel SAP and lab applications