Quality Control Analyst, Microbiology

OXB; North East; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading viral vector manufacturing company in the UK seeks a Quality Control Analyst, Microbiology. You will perform cGMP microbial testing and engage in environmental monitoring, ensuring compliance and efficiency. The ideal candidate has a BS in Microbiology and at least 3 years of experience in a cGMP environment. Competitive benefits and a collaborative culture are offered.

Benefits

Competitive total reward packages

Wellbeing programs

Career development opportunities

Supportive culture

Qualifications

• Minimum BS in Microbiology or related scientific field.
• 3+ years of experience in a cGMP/GxP environment preferred.
• Hands-on experience in microbiological methods.

Responsibilities

• Perform cGMP microbial testing, including endotoxin and bioburden.
• Review and evaluate raw data from analytical methods.
• Lead and support laboratory deviations and investigations.

Skills

cGMP microbial testing

Environmental monitoring

Data review and trending

SOPs authoring and review

Technical documentation

Collaboration skills

Education

BS in Microbiology or related scientific field

Job description

Overview

Join Us in Changing Lives

OXB is a quality and innovation-led viral vector CDMO with a mission to enable its clients to deliver life changing therapies to patients around the world. We’re expanding our US footprint with a new commercial-scale viral vector facility in Durham, North Carolina and have opportunities to join our team.

We’re currently recruiting for a Quality Control Analyst, Microbiology to join our Quality Control team. In this role, you will perform microbiological methods, environmental monitoring, data review and trending, and implementation of GMP operational systems—ensuring a compliant and efficient QC laboratory environment. You’ll collaborate cross-functionally and play a key part in advancing our mission.

Responsibilities

• Perform cGMP microbial testing, including endotoxin, bioburden, and environmental monitoring.
• Review and evaluate raw data from analytical methods at a peer or technical review level, including sample authorization.
• Author, review, and/or approve SOPs, policies, and technical reports with guidance as needed.
• Lead and support laboratory deviations and investigations (IA, OOS, AR), including assessments, protocol/report authoring, and closure with minimal supervision.
• Lead, author, perform, review, and/or approve equipment validations with limited guidance.
• Implement, lead, and/or support operational systems, including equipment/instrument maintenance and calibration, alarm monitoring, sample handling/tracking, data integrity and control, cGMP documentation, LIMS, laboratory audits, and method training.
• Execute phase-appropriate test method validation protocols as required.
• Participate in providing information for regulatory filings and inspections.
• Lead and support CAPA and continuous improvement initiatives.

Qualifications

• Education: Minimum BS in Microbiology or related scientific field.
• Experience: 3+ years of experience in a cGMP/GxP environment preferred.
• Hands-on experience in environmental monitoring, facility qualification, bioburden, endotoxin, and other microbiological methods.
• Demonstrated strong initiative, technical capability, and scientific leadership.
• Experience authoring and reviewing SOPs and technical documentation.
• Excellent organizational, analytical, and communication skills with a proactive, collaborative approach.
• A self-directed individual who thrives in a fast-paced, goal-oriented environment.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the United States.

About Us

OXB is a quality and innovation-led viral vector CDMO with a mission to enable its clients to deliver life changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, we have more than 30 years of experience in viral vectors; the driving force behind the majority of gene therapies.

OXB collaborates with some of the world’s most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. Our capabilities span from early-stage development to commercialisation, supported by robust quality-assurance systems, analytical methods, and depth of regulatory expertise.

Why Join Us

• 💸 Competitive total reward packages
• 🧘 Wellbeing programs that support your mental and physical health
• 🚀 Career development opportunities to help you grow and thrive
• 🤝 Supportive, inclusive, and collaborative culture
• 🧪 State-of-the-art labs and manufacturing facilities
• 🌍 A company that lives its values: Responsible, Responsive, Resilient, Respect

We want you to feel inspired every day. At OXB, we’re future-focused and growing fast. We succeed together—through passion, commitment, and teamwork.

Ready to Make a Difference?

We offer: