This role supports critical logistics center operations including goods receipt, sampling, and drug substance put away within a next-generation manufacturing facility
Job Summary
This role supports critical logistics center operations including goods receipt, sampling, and drug substance put away within a next-generation manufacturing facility.
The position requires overseeing quality assurance aspects of material receipt and batch disposition in strict accordance with GMP regulations.
Candidates must possess strong communication skills to facilitate inspections, audits, and collaborate with cross-functional teams to ensure seamless material flow.
Matching Summary
This role supports critical logistics center operations including goods receipt, sampling, and drug substance put away within a next-generation manufacturing facility.
Skills & Requirements
Must-have
cGMP and FDA regulatory knowledge
Material batch release processes
Deviation and CAPA investigation
SAP and Trackwise/Veeva usage
Change control collaboration
Nice-to-have
Continuous improvement initiatives
Cross-functional team leadership
Strong analytical problem-solving skills
Time on The Floor activities support
Key Requirements
Level 7 qualification or higher in Science or Engineering
Minimum 3 years QA experience in pharma/biotech
Experience with QMS software like SAP and Trackwise