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- Tasks: Lead compliance activities and ensure adherence to GxP standards.
- Company: Join a leading pharmaceutical company dedicated to quality and compliance.
- Benefits: Enjoy a collaborative culture with opportunities for continuous improvement and professional growth.
- Why this job: Be a key player in fostering a strong compliance culture and making a real impact.
- Qualifications: Strong QA experience in pharmaceuticals, especially in GMP/GDP and data integrity.
- Other info: Ideal for those passionate about quality management and regulatory compliance.
The predicted salary is between 48000 - 84000 £ 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
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 compliance roles. 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 and quality improvement initiatives in your previous roles. Highlighting your hands-on experience will showcase your capability to lead QMS activities effectively.
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 Strong Cover Letter: In your cover letter, clearly articulate your understanding of GxP standards and how your background aligns with the responsibilities of the Quality Assurance Compliance Manager role. Mention specific examples of your expertise in data integrity and compliance.
Showcase Communication Skills: Since this role requires strong stakeholder engagement, include examples in your application that demonstrate your confident communication skills. Highlight instances where you collaborated with cross-functional teams to achieve compliance goals.
Highlight Relevant Tools Experience: If you have experience with electronic quality systems like TrackWise or LIMS, make sure to mention this in your application. This will show that you are familiar with the tools that are beneficial for the role.
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.
✨Demonstrate Leadership Skills
This role is about leading compliance activities, so be prepared to share your experiences in leading teams and driving continuous improvement initiatives. Use specific examples to illustrate your leadership style.
✨Familiarity with Quality Systems
If you have experience with electronic quality systems like TrackWise or LIMS, mention it! Discuss how these tools have helped you maintain compliance and improve processes in your previous roles.
