Production Operator

ZipRecruiter; Stevenage; On-site; GBP 28,000 - 40,000; Full time

Job summary

A leading biotech company is seeking an Operator II for its production team in Stevenage. This permanent, on-site role involves ensuring compliance with GMP regulations and supporting the manufacture of cell-based therapies. Successful candidates will have at least 2 years of GMP experience and thrive in a shift-based environment, contributing to innovative cancer treatments.

Qualifications

• Minimum 2 years GMP manufacturing cleanroom experience.
• Ability to follow detailed instructions.
• Experience working in a shift-based environment.

Responsibilities

• Execute production processes in line with GMP and GDP requirements.
• Conduct raw material transfers and environmental monitoring.
• Perform cell culture activities and aseptic manipulations.

Skills

GMP manufacturing experience

Detailed understanding of GxP

Environmental health & safety requirements

Problem-solving methodologies

Job description

Job Description

*Operator II, Production - Stevenage - On-site, Permanent*

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

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- 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 [e-mail]