Production Operator

JR United Kingdom; Watford; On-site; GBP 25,000 - 35,000; Full time

Job summary

A leading biotech company in Watford is seeking a Production Operator to join their GMP manufacturing team. This shift-based role involves ensuring high-quality production of cell-based therapies while complying with regulatory and safety standards. Ideal candidates will have at least two years of GMP experience and a passion for biotechnology.

Qualifications

• Minimum 2 years GMP manufacturing cleanroom experience.
• Ability to follow detailed instructions and make quality-critical decisions.
• Experience in a shift-based environment preferred.

Responsibilities

• Execute production processes and operate associated equipment in line with GMP.
• Conduct raw material transfers and maintain cleanroom environments.
• Support batch review execution and lead operational deviations.

Skills

GMP manufacturing

Cell culture activities

Problem-solving

Documentation compliance

Environmental monitoring

Job description

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Production Operator, watford, hertfordshire

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Client:

Skills Alliance

Location:

watford, hertfordshire, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

4

Posted:

28.06.2025

Expiry Date:

12.08.2025

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Job Description:

Are you an experienced Production Operator interested in joining our biotech client that is leading the way in developing innovative CAR-T cell therapies for cancer treatment?

Our client is looking for a highly motivated Operator II to join their GMP manufacturing team. This is a shift-based role that involves weekends and shifts that fall within the operating hours of 6AM-10PM. You will play a key role in ensuring the production of high-quality cell-based products while maintaining compliance with GMP regulations, safety standards and company procedures.

Responsibilities:

• Execute production processes and operate associated equipment in line with GMP and GDP requirements.
• Maintain cleanroom environments through sterile room maintenance, hydrogen peroxide vapour gassing, and environmental monitoring (EM).
• Conduct raw material transfers, particulate cleaning and disinfection, material receipt, and drug product shipment.
• Accurately complete documentation and data entry, ensuring compliance with regulatory standards.
• Perform cell culture activities including sampling, counting, washing, activation, feeding, harvesting, and magnetic enrichment/depletion (MACS).
• Carry out aseptic manipulations in Grade A environments and meet associated BROTH qualification (OAQ) standards.
• Support batch review execution and collaborate with cross-functional teams to ensure smooth workflow.
• Lead or support operational deviations, process risk assessments, and continuous improvement (CI) initiatives.
• Assist in the authoring and revision of SOPs, SWIs, and risk assessments to maintain process efficiency and compliance.
• Provide guidance and mentoring to junior team members, supporting their training and development.
• Follow all SOPs/SWI applicable & in which the individual has been trained and always act in compliance with GMP & to proactively raise any issues

Required Experience

• Minimum 2 years GMP manufacturing cleanroom experience
• Exposure to high performance/stress conditioned work
• Demonstrate detailed understanding of GxP / sterile / ATMP production
• Demonstrate proficiency in environmental, health & safety requirements
• Ability to follow detailed instructions and make quality-critical decisions

Preferred Experience:

• Experience working in a shift-based environment
• Familiarity with problem-solving methodologies like Lean Six Sigma

This role offers an exciting opportunity to be part of an innovative biotech company, contributing to the manufacture of next-generation cell-based therapies. If you're passionate about GMP manufacturing and eager to make a difference, we’d love to hear from you! Reach out on LinkedIn or send your CV to [emailprotected]