QC Manager

RBW Consulting LLP; England; On-site; GBP 70,000 - 95,000; Full time

Job summary

RBW Consulting LLP in Surrey is partnering with a major pharmaceutical client to recruit a QC Manager who will oversee all site Quality Control activities, with a focus on method development oversight and team leadership.

The role requires a solid GMP-regulated laboratory background, experience with validation lifecycles, and the ability to mentor a largely new team while maintaining day-to-day operations in the lab and supporting OOS investigations and equipment maintenance.

Qualifications

• GMP-regulated pharmaceutical environment experience.
• Experience managing validation activities and supporting method validation programmes.
• Strong laboratory background with analytical testing oversight.
• Experience with HPLC and/or GC.
• 3+ years of people management experience.

Responsibilities

• Lead QC activities and scheduling on site.
• Oversee method development and validation lifecycle.
• Provide mentorship and develop a high-performing team.
• Coordinate with site leadership to establish best practices.
• Handle out-of-specification investigations and troubleshooting.
• Maintain equipment and supervise laboratory activities.

Skills

Quality Control Leadership

Team Leadership

GMP Knowledge

Validation Activities

OOS Investigations

Analytical Chemistry

Tools

HPLC

GC

Job description

QC Manager - Surrey I am partnered exclusively with an international advanced pharmaceutical company that are continuing to expand operations both in terms of product delivery and site presence across the UK. This specific hire will take management and scheduling responsibilities for all site Quality Control (QC) activities, with a strong focus on method development oversight and team leadership. A solid understanding of the full validation lifecycle is essential, alongside strong regulatory knowledge and an analytical chemistry background. Whilst this will not be a hands-on role day to day, given the size of the unit, you will need to be comfortable spending time in the laboratory and supporting the team, particularly with out-of-specification investigations, method development, and validation activities. A strong laboratory background is essential, with experience in equipment maintenance, troubleshooting, and validation highly desirable. This is an excellent opportunity for an experienced people leader to help shape and develop a growing QC function. With approximately 75% of the team being newly recruited, you will have a unique opportunity to build team culture, establish best practices, and develop a high-performing department alongside site leadership. We are ideally looking for someone with around three years' management experience who can bring proven leadership skills and confidently manage the operational and people aspects of the role from day one.

Key Experience

Experienced QC Manager, Laboratory Manager, QC Supervisor or Senior QC/Analytical Chem professional within a GMP-regulated pharmaceutical environment

Strong laboratory experience, including equipment maintenance, troubleshooting, and analytical testing oversight

Experience managing validation activities and supporting method validation programmes

Technical experience with analytical techniques such as HPLC and/or GC

Previous people management experience, ideally 3+ years

Proven ability to lead, develop, and mentor teams

Strong organisational, planning, and resource scheduling skills

Excellent understanding of GMP requirements and pharmacopoeial standards

QC Manager, Quality Control, Analytical Chemistry, HPLC, GC, GMP, Method Validation, Equipment Maintenance, Laboratory Management, Team Leadership, Validation, OOS Investigations, Pharmacopoeia, QC Leadership, Pharmaceutical Manufacturing.