The role involves coordinating day-to-day In-Process laboratory activities to ensure testing is delivered to schedule and compliance targets are met
Job Summary
The role involves coordinating day-to-day In-Process laboratory activities to ensure testing is delivered to schedule and compliance targets are met.
Candidates will be responsible for writing, maintaining, and electronically building In-Process testing methods for various pharmaceutical operations including solvent recovery and cleaning validation.
The position requires acting as the main auditee and supporting internal and external regulatory inspections while driving continuous improvement initiatives.
Matching Summary
The role involves coordinating day-to-day In-Process laboratory activities to ensure testing is delivered to schedule and compliance targets are met.
Skills & Requirements
Must-have
cGMP environment experience
In-Process laboratory coordination
Analytical method development
LIMS and Empower systems
Deviation management and CAPA
Regulatory inspection support
Nice-to-have
Continuous improvement initiatives
Cross-functional team collaboration
Strong stakeholder communication
Problem-solving skills
Deputising for Team Lead
Key Requirements
Minimum BSc in Chemistry or related Life Sciences
Solid analytical laboratory experience in cGMP
Experience with GMP quality systems and change control