Actionus
Quality Control Lead
Skills
1 month ago
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Important information
Contract type:
Permanent
Location:
United Kingdom
Work mode:
Onsite
Published on:
30 September 2026
What they need
The role
This Quality Control Lead role offers a permanent position in West, London, overseeing QC operations for a stem cell therapy manufacturing facility. You will be responsible for scaling a new team, quality control and final product release under an MHRA Manufacturer Specials licence, ensuring full compliance with GMP Annex 1 and HTA requirements. The successful candidate will establish approved licence status, environmental monitoring programmes and validate QC systems for advanced therapy manufacturing.
Responsibilities
- Establish and oversee cleanroom environmental monitoring programmes aligned with MHRA GMP Annex 1 standards.
- Develop and execute QC testing protocols including sterility, mycoplasma, endotoxin, and cell characterisation.
- Lead qualification and validation activities for Grade A to D cleanroom environments including air and water testing.
- Review batch records and sign off finished product release in line with MHRA requirements for specials manufacturing.
- Manage raw material testing, release protocols, and stability studies for stem cell lines under HTA guidelines.
- Lead investigations into out of specification results, performing root cause analysis and implementing CAPAs.
- Represent the QC department and processes during formal MHRA and HTA regulatory inspections.
What you'll need
- Degree in pharmacy, microbiology, biotechnology, or a closely related life science discipline.
- Minimum of 5 years practical experience in a GMP regulated manufacturing environment under MHRA oversight.
- Extensive hands on experience with human cell culture, stem cell lines, and aseptic techniques.
- Detailed knowledge of cleanroom qualification and environmental monitoring adhering to GMP Annex 1.
- Proven experience preparing laboratories for HTA inspections and maintaining HTA licensing readiness.
- Eligibility to be named as the person responsible for QC on an MHRA MS or MIA licence.
- Standard DBS clearance for working within regulated life science environments.
Send your CV or contact Actionus for further details.
Pay: £80,000.00-£100,000.00 per year
Work Location: In person
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