Quality Control Laboratory Manager

JR United Kingdom; Croydon; On-site; GBP 50,000 - 70,000; Full time

Job summary

A growing international pharmaceutical company seeks a Quality Control Laboratory Manager in Croydon. This key role focuses on managing QC activities, emphasizing method validation and regulatory compliance, while leading a dynamic team to drive quality standards and performance on site. Ideal candidates will have extensive experience in QC within a GMP setting.

Qualifications

• Experienced QC/Analytical Chemistry manager or supervisor in a pharmaceutical GMP environment.
• Technical experience with method validation and regulatory compliance required.

Responsibilities

• Manage and schedule all site Quality Control (QC) activities.
• Provide oversight on method development and ensure team support on out-of-specification challenges.

Skills

Leadership

Analytical Chemistry

Quality Control

Method Development

Regulatory Knowledge

Tools

HPLC

GC

Job description

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Quality Control Laboratory Manager, Croydon

Client: RBW Consulting

Location: 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:

QC Manager

I am partnered exclusively with an international advanced pharmaceutical company that is expanding its operations across the UK.

This role involves managing and scheduling all site Quality Control (QC) activities, with a focus on method development oversight and team leadership. A comprehensive understanding of the full validation lifecycle, from start to finish, and solid regulatory knowledge from an analytical chemistry perspective are essential.

While this position is primarily managerial, you should be comfortable supporting the laboratory team, especially with out-of-specification challenges and validation activities.

If you're seeking a varied role where you can make a significant impact on your site and influence the QC team's delivery and growth, please apply or contact Mark Bux-Ryan for more information.

Key experience:

• Experienced QC/Analytical Chemistry manager or supervisor in a pharmaceutical GMP environment
• Technical experience with HPLC, GC
• Strong understanding of pharmacopoeia
• Experience in method validation 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