Are you a microbiology-focused QC professional with experience in a cGMP environment—or a recent graduate with hands-on microbiology lab experience?
SRG have a fantastic opportunity to join a successful and expanding organisation in the Central Belt of Scotland, supporting GMP microbiology and quality control activities within the Quality department.
The Role:
Support and maintain QC microbiology quality systems and documentation (SOPs, forms, logbooks) in line with cGMP
Perform and/or review microbiology testing and data, including Environmental Monitoring (viable/non-viable), bioburden and endotoxin testing
Support microbiology aspects of stability studies (sample coordination, testing plans, trending and reporting)
Approve and release incoming raw materials/consumables where microbiological controls apply
Manage QC investigations and CAPAs related to microbiology results (OOS/OOT, EM excursions, contamination events)
Support method technical transfer/verification/validation for microbiological methods (e.g., bioburden, endotoxin, EM)
Carry out routine lab activities such as media preparation, growth promotion, sample preparation, incubation, colony counting and basic microbial identification
Support the ongoing maintenance and oversight of subcontract/contract testing facilities (as required), including document review and quality agreements
Trend and interpret microbiology/QC data to identify shifts, recurring issues and improvement opportunities
Ensure all QC microbiology processes are compliant with cGMP guidance and site procedures, maintaining data integrity at all times
Skills:
Strong communication skills, with the confidence to document and present microbiology/QC findings clearly
Able to work well as part of a team in a GMP-regulated laboratory environment
High attention to detail and a right-first-time approach to documentation and data integrity
Good time management and planning skills, able to prioritise routine testing alongside investigations
Requirements:
Open to experienced QC Microbiology Analysts (industry) or graduates with hands-on microbiology laboratory experience (placement, internship, university lab or similar)
Experience with one or more of the following is beneficial: Environmental Monitoring, bioburden, endotoxin testing, media preparation and basic microbial identification
Exposure to GMP/GLP or other regulated environments is advantageous (training provided where needed)
Experience of supporting a QMS and assisting with deviations/investigations/CAPA is desirable
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