QC Supervisor

Posted 7 Days Ago
Be an Early Applicant
Heywood, Rochdale, Greater Manchester, England, GBR
In-Office
Mid level
Biotech • Pharmaceutical
The Role
Lead and manage daily QC microbiology laboratory operations in a regulated culture media manufacturing environment. Supervise and develop staff, plan workloads, review and authorise test results and records, maintain equipment and retained samples, ensure compliance with GMP/GLP and data integrity, support audits and investigations, and drive CAPA and continuous improvement activities to enable timely product release.
Summary Generated by Built In

It's fun to work in a company where people truly believe in what they are doing!


We are seeking a Quality Control Supervisor to lead the day-to-day operation and performance of a Quality Control Laboratory within a regulated culture media manufacturing environment. This is a key leadership role responsible for ensuring microbiological testing, laboratory documentation, equipment control, retained samples and workflow planning are managed safely, accurately and efficiently to support timely product release and customer supply. Working closely with Quality Assurance, Production, Planning, Technical Support and Operations, you will help maintain high standards of compliance, audit readiness, data integrity and continuous improvement.

Key Responsibilities
  • Supervise daily QC Laboratory operations, planning and prioritising workloads to ensure compliant and timely testing of finished products, raw materials, in-process samples and other applicable samples.
  • Lead, coach and develop QC laboratory team members, ensuring staff are trained, competent and authorised to perform assigned activities safely and accurately.
  • Review and authorise QC test results, laboratory records and associated documentation within delegated authority, ensuring compliance with approved methods, SOPs, specifications and data integrity principles.
  • Maintain laboratory compliance and audit readiness, supporting internal audits, external audits, customer audits and UKAS or accreditation assessments where applicable.
  • Oversee laboratory equipment, consumables, reagents, media, reference cultures, retained samples and controlled documentation to ensure effective availability, control and suitability for use.
  • Support investigations, CAPAs, deviations, non-conformances, complaints, out-of-specification results and continuous improvement initiatives to enhance safety, quality, efficiency and turnaround times.
Job Requirements
  • Degree or equivalent qualification in Microbiology, Biomedical Science, Food Science, Biological Sciences or a related scientific discipline.
  • At least 3 years' experience in a busy microbiology laboratory, ideally within manufacturing, food safety, pharmaceutical, medical device, diagnostics or another regulated production environment.
  • Practical experience of microbiological testing, culture media testing, aseptic technique and accurate laboratory documentation.
  • Experience working within a Quality Management System, with a good understanding of GMP/GLP principles, data integrity and laboratory compliance expectations.
  • Previous experience supervising, mentoring or coordinating laboratory staff and laboratory workloads, with strong planning and organisational skills.
  • Strong understanding of microbiology laboratory health and safety requirements, including COSHH, biological safety, risk assessments, PPE and safe systems of work.
What We Offer
  • A senior supervisory role with meaningful responsibility in a regulated scientific manufacturing environment.
  • The opportunity to lead and develop a skilled QC laboratory team while contributing to product quality, customer supply and regulatory compliance.
  • Cross-functional collaboration with Quality Assurance, Production, Planning, Technical Support, EHS and Operations teams.
  • Involvement in audits, investigations, process improvements, method implementation and laboratory performance initiatives.
  • A standard benefits package and a professional working environment focused on safety, quality, compliance and continuous improvement.

We welcome applications from candidates who meet the essential requirements and are committed to high standards of laboratory quality, safety and leadership. If you are ready to take the next step in your QC career and contribute to a regulated manufacturing environment where accuracy, collaboration and continuous improvement matter, we'd love to hear from you. Join our team and help support the delivery of safe, reliable and compliant products to customers.

Come Be Part Of A Mission that Matters!

From inside the farm gate to our dinner plates, Neogen protects the world’s food supply. Through a variety of animal healthcare products, to food safety solutions for dangerous bacteria, allergens, toxins, drug residues and much more, Neogen is there — and you can be too.

Skills Required

  • Degree or equivalent in Microbiology, Biomedical Science, Food Science, Biological Sciences or related scientific discipline
  • At least 3 years' experience in a busy microbiology laboratory in manufacturing, food safety, pharmaceutical, medical device, diagnostics or other regulated environment
  • Practical experience of microbiological testing, culture media testing, aseptic technique and accurate laboratory documentation
  • Experience working within a Quality Management System with understanding of GMP/GLP principles and data integrity
  • Previous experience supervising, mentoring or coordinating laboratory staff and workloads with strong planning and organisational skills
  • Understanding of microbiology laboratory health and safety requirements including COSHH, biological safety, risk assessments, PPE and safe systems of work
  • Experience supporting investigations, CAPAs, deviations, non-conformances, complaints and out-of-specification results
  • Ability to review and authorise QC test results, laboratory records and associated documentation within delegated authority

Neogen Corporation Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Neogen Corporation and has not been reviewed or approved by Neogen Corporation.

  • Healthcare Strength The benefits suite includes comprehensive medical, dental and vision coverage, plus disability, life insurance, and an Employee Assistance Program. These core coverages are consistently described as a relative bright spot.
  • Retirement Support A defined-contribution 401(k) with company match and immediate vesting is highlighted, alongside standard retirement and savings programs. This structure provides clear baseline retirement support for eligible roles.
  • Equity Value & Accessibility An employee stock purchase plan offers discounted access to company shares. This adds an ownership pathway that complements cash compensation.

Neogen Corporation Insights

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The Company
HQ: Lansing, MI
1,160 Employees
Year Founded: 1982

What We Do

NEOGEN Corporation develops and markets products dedicated to food and animal safety. The company’s Food Safety Division markets dehydrated culture media and diagnostic test kits to detect foodborne bacteria, natural toxins, genetic modifications, food allergens, drug residues, plant diseases and sanitation concerns. NEOGEN’s Animal Safety Division markets a complete line of diagnostics, veterinary instruments, veterinary pharmaceuticals, nutritional supplements, disinfectants and rodenticides.

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