Quality Control Laboratory Manager

JR United Kingdom; London; On-site; GBP 45,000 - 70,000; Full time

Job summary

A leading international pharmaceutical company is seeking a Quality Control Laboratory Manager for their London (Croydon) site. The role involves overseeing QC activities, ensuring full validation lifecycle compliance, and supporting laboratory operations during critical issues. Candidates should possess experience in GMP environments with strong analytical chemistry skills. This dynamic position offers opportunities to significantly impact QC functions and contribute to the company's expansion.

Qualifications

• Experience managing QC or Analytical Chemistry in pharma GMP environments.
• Comfortable supporting laboratory activities during out-of-specification issues.
• Comprehensive understanding of validation lifecycles and regulatory requirements.

Responsibilities

• Manage and schedule all site QC activities.
• Provide method development oversight and team leadership.
• Contribute to the company's growth through QC operations influence.

Skills

Analytical Chemistry

Leadership

Quality Control

Method Validation

Pharmacopoeia Knowledge

Tools

HPLC

GC

Job description

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Quality Control Laboratory Manager, London (Croydon)

Client: RBW Consulting

Location: London (Croydon), United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views:

2

Posted:

06.06.2025

Expiry Date:

21.07.2025

Job Description:

We are seeking an experienced QC Manager for a leading international pharmaceutical company expanding across the UK. This role involves managing and scheduling all site Quality Control (QC) activities, with a strong focus on method development oversight and team leadership. A comprehensive understanding of the full validation lifecycle and regulatory requirements from an analytical chemistry perspective is essential.

While the role is primarily managerial, the successful candidate should be comfortable supporting laboratory activities, especially during out-of-specification issues and validation processes, given the team size.

If you are looking for a dynamic position where you can influence QC operations and contribute to the company's growth, please apply below or contact Mark Bux-Ryan for more information.

Key Experience:

• Experienced QC/Analytical Chemistry manager or supervisor within a pharmaceutical GMP environment
• Technical experience with HPLC, GC
• Strong understanding of pharmacopoeia
• Experience with method validation activities from start to finish

Keywords: QC, quality, control, chromatography, HPLC, GC, chemistry, analytical, method validation, development, IQ, OQ, PQ, TLC, supervisor, leader, manager, group lead