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- Tasks: Lead compliance activities and ensure adherence to GxP standards in a dynamic environment.
- Company: Join a leading pharmaceutical company committed to quality and compliance excellence.
- Benefits: Enjoy competitive pay, professional development opportunities, and a collaborative work culture.
- Why this job: Be part of a team that shapes a strong compliance culture and drives continuous improvement.
- Qualifications: Strong QA experience in pharmaceuticals, with expertise in data integrity and quality systems required.
- Other info: Opportunity to collaborate with cross-functional teams and influence quality initiatives across the site.
The predicted salary is between 43200 - 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
Locations
Quality Assurance Compliance Manager employer: Nexia Life Sciences
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 maintaining high-quality standards.
✨Tip Number 2
Network with professionals in the Quality Assurance field, especially those who have experience in data integrity and compliance. Engaging with industry experts can provide valuable insights and may even lead to referrals for the position.
✨Tip Number 3
Stay updated on the latest trends and technologies in quality management systems, particularly electronic quality systems like TrackWise and LIMS. Being knowledgeable about these tools 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 expertise and fit for the role.
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, especially in relation to GxP standards.
Highlight Relevant Skills: Clearly outline your expertise in data integrity and compliance within regulated environments. Include any experience with electronic quality systems like TrackWise or LIMS, as this will strengthen your application.
Showcase Leadership Experience: Since this is a leadership role, be sure to include examples of your leadership skills. Discuss how you've collaborated with cross-functional teams and contributed to quality initiatives in past 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, be ready to explain best practices and how you've implemented them in past positions. Highlight any training or mentoring you've provided to teams on this topic.
✨Prepare for Scenario-Based Questions
Expect questions that require you to think critically about quality oversight, such as handling investigations or CAPAs. Prepare examples that demonstrate your problem-solving skills and ability to maintain compliance under pressure.
✨Highlight Cross-Functional Collaboration
Emphasise your experience working with various departments like QA, Manufacturing, and IT. Share specific instances where your collaboration led to improved compliance or quality outcomes, showcasing your stakeholder engagement skills.
