The role involves coordinating day-to-day In-Process laboratory activities to ensure testing is delivered to schedule while meeting strict compliance targets
Job Summary
The role involves coordinating day-to-day In-Process laboratory activities to ensure testing is delivered to schedule while meeting strict compliance targets.
Candidates will be responsible for writing and maintaining electronic testing methods for solvents, drug substances, and environmental monitoring across a global hub facility.
The position requires acting as the main auditee for regulatory inspections and supporting investigations including root cause analysis and CAPA implementation.
Matching Summary
The role involves coordinating day-to-day In-Process laboratory activities to ensure testing is delivered to schedule while meeting strict compliance targets.
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
Experience with change control and deviation management
Nice-to-have
Excellent organisation planning and time-management skills
Strong written and verbal communication abilities
Demonstrated problem-solving and continuous improvement skills
Ability to work cross-functionally and deputise for Team Lead
Key Requirements
Minimum BSc in Chemistry or related Life Sciences discipline
Solid analytical laboratory experience in a cGMP environment
Competence with LIMS, Empower, Tiamo/LabX data systems