Quality Assurance Compliance Manager

ZipRecruiter; Guildford; On-site; GBP 50,000 - 80,000; Full time

Job summary

An established industry player is seeking a Quality Management System Lead to ensure compliance with GxP standards. This pivotal role involves overseeing QMS activities, advising on data integrity, and collaborating with cross-functional teams to foster a culture of quality. Ideal candidates will have a strong background in pharmaceutical quality assurance, particularly in GMP/GDP, and be adept at engaging stakeholders. Join a dynamic team dedicated to maintaining high standards of quality and compliance in a regulated environment. This is an exciting opportunity to make a significant impact in the field of quality management.

Qualifications

• Strong background in pharmaceutical QA and compliance.
• Experience in validation and quality systems management.

Responsibilities

• Lead QMS compliance activities and continuous improvement initiatives.
• Provide quality oversight on investigations and audit readiness.

Skills

Pharmaceutical QA

GMP/GDP Compliance

Data Integrity

Stakeholder Engagement

Quality Oversight

Tools

TrackWise

LIMS

Job description

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