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- Tasks: Lead compliance activities and ensure adherence to GxP standards.
- Company: Join a leading pharmaceutical company committed to quality and compliance.
- Benefits: Enjoy a collaborative culture, professional growth opportunities, and potential remote work options.
- Why this job: Be a key player in fostering a strong compliance culture and making a real impact.
- Qualifications: Strong QA experience in pharmaceuticals, with expertise in data integrity and quality systems.
- Other info: Ideal for those passionate about quality assurance and regulatory compliance.
The predicted salary is between 48000 - 72000 £ per year.
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
Contact Detail:
Nexia Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Compliance Manager
✨Tip Number 1
Familiarise yourself with GxP standards and the specific compliance requirements relevant to the pharmaceutical industry. This knowledge will not only help you in interviews but also demonstrate your commitment to quality assurance.
✨Tip Number 2
Network with professionals in the QA field, especially those who have experience in data integrity and compliance. Engaging with industry experts can provide insights into the role and may even lead to referrals.
✨Tip Number 3
Stay updated on the latest trends and technologies in quality management systems. Being knowledgeable about electronic quality systems like TrackWise or LIMS can set you apart from other candidates.
✨Tip Number 4
Prepare to discuss specific examples of how you've contributed to compliance initiatives in previous roles. Highlighting your hands-on experience with CAPAs, change controls, and audit readiness will showcase your suitability for the position.
We think you need these skills to ace Quality Assurance Compliance Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in pharmaceutical QA, particularly focusing on GMP/GDP. Emphasise any roles where you led QMS compliance activities or worked with validation and quality systems.
Craft a Compelling Cover Letter: In your cover letter, explain why you are passionate about quality assurance and compliance. Mention specific examples of how you've contributed to a strong compliance culture in previous roles, and how your expertise aligns with the responsibilities of the Quality Assurance Compliance Manager.
Highlight Relevant Skills: Clearly outline your skills related to data integrity and compliance. If you have experience with electronic quality systems like TrackWise or LIMS, make sure to mention this as it could set you apart from other candidates.
Showcase Leadership Experience: Since this is a leadership role, be sure to include any relevant leadership experiences. Discuss how you've successfully collaborated with cross-functional teams and contributed to quality initiatives in your previous positions.
How to prepare for a job interview at Nexia Life Sciences
✨Understand GxP Standards
Make sure you have a solid grasp of GxP standards and how they apply to Quality Management Systems. Be prepared to discuss specific examples of how you've ensured compliance in previous roles.
✨Showcase Your Data Integrity Knowledge
As a data integrity subject matter expert, you should be ready to explain best practices and common pitfalls. Share your experiences in educating teams on these topics to demonstrate your expertise.
✨Highlight Your Leadership Skills
This role is about leading compliance activities, so be sure to highlight your leadership experience. Discuss how you've successfully led teams or projects in the past, particularly in a quality assurance context.
✨Prepare for Cross-Functional Collaboration
Collaboration is key in this role. Think of examples where you've worked closely with QA, Manufacturing, Validation, or IT teams. Be ready to discuss how you navigated challenges and achieved successful outcomes together.
