Quality Assurance Compliance Manager

JR United Kingdom; Guildford; On-site; GBP 40,000 - 80,000; Full time

Job summary

An established industry player is seeking a Quality Assurance Compliance Manager to lead QMS compliance activities in Guildford. This pivotal role is essential for maintaining adherence to GxP standards and fostering a culture of quality across operations. You will collaborate with various functions to ensure regulatory expectations are met while providing oversight on investigations and audits. If you have a strong background in pharmaceutical QA and a passion for quality management, this is an exciting opportunity to make a significant impact in a dynamic environment.

Qualifications

• Strong experience in pharmaceutical QA with a focus on GMP/GDP.
• Proven expertise in data integrity and compliance in regulated environments.

Responsibilities

• Lead QMS compliance activities focusing on continuous improvement.
• Act as the site’s data integrity subject matter expert.

Skills

Pharmaceutical QA

GMP/GDP Compliance

Data Integrity

Stakeholder Engagement

Quality Oversight

Tools

TrackWise

LIMS

Job description

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Quality Assurance Compliance Manager, guildford

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Client:

Nexia Life Sciences

Location:

guildford, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

3

Posted:

05.05.2025

Expiry Date:

19.06.2025

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Job Description:

Overview:

This leadership role is central to ensuring the site's Quality Management System remains compliant with GxP standards. You’ll act as the site lead for QMS and data integrity, supporting ongoing compliance across validation, documentation, and quality processes. The role sits within the Quality leadership team and plays a key part in building a strong compliance culture across the UK site and affiliate operations.

Key Responsibilities:

• Lead QMS compliance activities across the site, focusing on continuous improvement and adherence to GxP
• Act as the site’s data integrity subject matter expert, advising and educating teams on best practice
• Maintain and develop the site’s validation master plan
• Provide quality oversight on investigations, CAPAs, change controls, and audit readiness
• Collaborate closely with QA, Manufacturing, Validation, and IT functions to ensure systems and processes meet regulatory expectations
• Contribute to the Quality leadership team and support cross-functional quality initiatives

Ideal Experience:

• Strong experience in pharmaceutical QA, with a focus on GMP/GDP
• Background in validation and quality systems (e.g. change control, CAPA, audit prep)
• Proven expertise in data integrity and compliance within a regulated environment
• Confident communicator with solid stakeholder engagement skills
• Familiarity with electronic quality systems (e.g. TrackWise, LIMS) is beneficial