Quality Control Supervisor at Biochek UK Ltd
London, Essex - England, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

10 Nov, 26

Salary

55000.0

Posted On

03 Oct, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Pharmaceutical Manufacturing

Description

About the Role

As QC Supervisor, you’ll oversee the day-to-day activities of the Quality Control team, ensuring diagnostic products meet performance standards and are released on time. You’ll provide technical guidance, support the team’s development, and play a key role in upholding quality, safety, and compliance requirements across all QC workflows.

This is a great opportunity for someone with a strong laboratory background in ELISA or immunoassay testing, who enjoys leading people and improving processes.

Key Responsibilities

  • Lead and supervise QC Analysts, managing daily schedules and supporting individual development
  • Oversee QC testing of reagents, raw materials, and finished ELISA kits
  • Ensure data accuracy, compliance with SOPs, and adherence to GDP standards
  • Review and approve laboratory documentation, escalating issues where needed
  • Support investigations into deviations and non-conformances
  • Maintain audit readiness and assist with internal and external audits
  • Contribute to the implementation of process improvements and digital tools (e.g., LIMS)
  • Collaborate with R&D and Manufacturing to support operational continuity


What We’re Looking For

  • Degree in Biochemistry, Immunology, Biomedical Science, or related discipline
  • Substantial experience in a QC lab, ideally within diagnostics, biotech, or biopharma manufacturing
  • Hands-on experience with ELISA or immunoassay testing
  • Strong organisational and communication skills
  • Experience supervising or mentoring lab teams
  • A commitment to data integrity and continuous improvement


How To Apply:

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Responsibilities

About the Role

As QC Supervisor, you’ll oversee the day-to-day activities of the Quality Control team, ensuring diagnostic products meet performance standards and are released on time. You’ll provide technical guidance, support the team’s development, and play a key role in upholding quality, safety, and compliance requirements across all QC workflows.

This is a great opportunity for someone with a strong laboratory background in ELISA or immunoassay testing, who enjoys leading people and improving processes.

Key Responsibilities

  • Lead and supervise QC Analysts, managing daily schedules and supporting individual development
  • Oversee QC testing of reagents, raw materials, and finished ELISA kits
  • Ensure data accuracy, compliance with SOPs, and adherence to GDP standards
  • Review and approve laboratory documentation, escalating issues where needed
  • Support investigations into deviations and non-conformances
  • Maintain audit readiness and assist with internal and external audits
  • Contribute to the implementation of process improvements and digital tools (e.g., LIMS)
  • Collaborate with R&D and Manufacturing to support operational continuity


What We’re Looking For

  • Degree in Biochemistry, Immunology, Biomedical Science, or related discipline
  • Substantial experience in a QC lab, ideally within diagnostics, biotech, or biopharma manufacturing
  • Hands-on experience with ELISA or immunoassay testing
  • Strong organisational and communication skills
  • Experience supervising or mentoring lab teams
  • A commitment to data integrity and continuous improvement


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