Specialist, QC Microbiology
2 weeks ago
The role: Specialist, QC Microbiology at Bristol Myers Squibb UK & Ireland. This is a full-time permanent position within the QC Microbiology Laboratory. Reporting to the QC Microbiology Manager, the Specialist will support site activities related to Product Testing and Environmental/Utility Monitoring, performing testing of samples and laboratory duties in accordance with cGMP regulations.
Key Duties and Responsibilities- Perform Bioburden testing on Utility samples, Drug Substance and Raw Materials within required hold times.
- Perform Bacterial Endotoxin Testing on Utility samples, Drug Substance and Drug Product within required hold times.
- Carry out In-Process testing of critical lot related samples to support Manufacturing activities.
- Perform QC Environmental Monitoring in classified areas including lot related monitoring.
- Utility sampling including Water for Injection (WFI), Clean Steam and Compressed Air/Gas.
- Perform Growth Promotion testing of media lots entering the laboratory.
- Carry out identifications of Microorganisms isolated post testing activities.
- Carry out the Minute Mouse Virus by PCR for in-process samples.
- Complete all laboratory documentation in a timely and accurate manner.
- Ensure compliance with Standard Operating Procedures and Registered Specifications.
- Assist in authoring and reviewing documentation, including SOPs.
- Provide support to other departments to ensure qualification and production schedules are adhered to.
- Review Batch paperwork and reconciliation of analyses performed in the laboratory.
- Investigate alert/action limit excursions according to site procedures.
- Maintain a high standard of housekeeping and safety in the laboratory.
- Perform any other activities as indicated by the Microbiology Manager.
- Minimum of a Level 8 degree in Microbiology or related discipline.
- At least 1 year of experience in a pharmaceutical/healthcare laboratory or related technical function.
- A strong background in Microbiology and aseptic manufacturing is desirable but not essential.
- Excellent written and verbal communication skills.
- Ability to work in a team-based collaborative environment is essential.
Note: This candidate may be required to work a 24/7 or 12/7 shift pattern.
Why you should apply- You will help patients in their fight against serious diseases.
- You will be part of a company that encourages excellence and innovation, respects diversity, develops leaders and values its employees.
- You'll receive a competitive salary and benefits package including an annual bonus, pension contribution, family health insurance, 27 days annual leave, on-site gym access and life assurance.
On-site Protocol: BMS has an occupancy structure that determines where an employee is required to conduct their work. Site-essential roles require 100% onsite shifts; site-by-design roles may be eligible for a hybrid model with at least 50% onsite. Field-based and remote-by-design roles require the ability to travel as needed. BMS is committed to reasonable accommodations in the recruitment process and ongoing roles. For accommodations, contact See for the Equal Employment Opportunity statement. BMS supports vaccination and boosters as part of employee well-being. Jobs may involve considerations related to local laws and disclosures.
Seniority level: Associate
• Employment type: Full-time
• Job function: Quality Assurance
• Industry: Pharmaceutical Manufacturing
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