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This is a fantastic opportunity to gain wider exposure in a laboratory for a global pharmaceutical company. You will work Monday to Friday, 9am - 5pm, working closely with other QC Analysts, and work together to ensure we are releasing the highest quality products.
Job Responsibility:
Raise, track, and receipt purchase orders for microbiology consumables, media, reagents, standards, and services in accordance with approved suppliers and GMP procedures
Maintain the equipment master list for QC Micro
Lead the controlled inventory process for media, disinfectants, PPE, plates, sampling kits, and EM supplies
Perform cycle counts, FEFO/FIFO, expiry management, quarantine of nonconforming items, and proper storage
Maintain cleaning/disinfection agent rotation logs and concentration verification documentation
Prepare, issue, and archive controlled documents
Review lab records for completeness, ALCOA+ principles, and adherence to GDP
Assist with drafting risk assessments under direction of QC Micro SME
Arrange training, equipment downtime windows, vendor site access, and safety permits
Coordinate internal and vendor calibrations, IQ/OQ/PQ events, and preventive maintenance
Support periodic data integrity checks, audit trail reviews, and readiness for internal/external audits
Administratively support OOS/OOT/OOL/Deviation investigations
Execute tasks in LIMS systems
Requirements:
Degree in Microbiology / Science related course preferable but not essential
Experience in GMP/GLP or regulated QC laboratory environment
Familiarity with equipment calibration/maintenance processes and controlled documentation practices
Ideally experienced using Trackwise, PEGA, COUPA & LIMS