QC Manager- Pharmaceuticals

Capio Spine Center Stockholm; Hitchin; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading company in the pharmaceutical sector is seeking an experienced Quality Control (QC) Manager to oversee their QC department within a GMP-compliant environment. The successful candidate will possess a strong background in analytical testing, proven management experience, and a thorough understanding of GMP standards. This role is vital for ensuring the quality and safety of manufactured products, involving both leadership and technical responsibilities.

Qualifications

• Educated to degree level or higher in a related scientific discipline.
• Previous QC Management or Supervisory experience is essential.
• Experience within a GMP pharmaceutical environment.

Responsibilities

• Lead and manage the Quality Control team.
• Ensure timely and accurate analytical testing.
• Maintain a GMP-compliant laboratory environment.

Skills

HPLC operation

Analytical testing

Communication

Organization

Problem-solving

Education

Degree in Pharmaceutical Sciences

Degree in Chemistry

Degree in Biochemistry

Job description

Role:- QC Manager- Pharmaceutical

Location:- Hertfordshire-Onsite role

Salary:- Competitive salary (DOE)

Hours:- Monday -Friday (Days)

Russell Taylor Group are seeking an experienced and motivated Quality Control (QC) Manager to lead our client's QC department within a GMP-compliant pharmaceutical manufacturing environment. The ideal candidate will have a strong background in analytical testing (particularly HPLC, GC, TLC, etc.), demonstrated people management experience, and a solid understanding of GMP requirements. This role is critical in ensuring the quality, safety, and compliance of all products manufactured on site.

Key Responsibilities

1. Lead and manage the Quality Control team (currently 8 members).
2. Oversee and ensure timely and accurate analytical testing of raw materials, in-process samples, and finished products using techniques such as HPLC, GC, UV, and other validated methods.
3. Maintain a GMP-compliant laboratory environment, ensuring adherence to all SOPs and regulatory requirements.
4. Review and approve analytical data, Certificates of Analysis, and laboratory investigations.
5. Collaborate with QA, Production, Regulatory Affairs, and R&D departments to support product quality and continuous improvement initiatives.
6. Lead training and development of QC staff to ensure technical competence and regulatory compliance.
7. Drive laboratory efficiency, equipment qualification, and method validation activities.
8. Monitor and manage laboratory KPIs, workloads, and performance targets.

The Person:-

1. Educated to degree level or higher in Pharmaceutical Sciences, Chemistry, Biochemistry, or a related scientific discipline.
2. Previous QC Management or Supervisory experience is essential.
3. Experience working within a GMP pharmaceutical manufacturing environment.
4. Strong experience in HPLC operation, troubleshooting, and method development/validation.
5. Excellent communication, organizational, and problem-solving skills.

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