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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 GMP/GDP and data integrity.
- Other info: Opportunity to collaborate with cross-functional teams and influence quality initiatives.
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 regulations that govern the pharmaceutical industry. This knowledge will not only help you understand the role better but also demonstrate your commitment to compliance during discussions.
✨Tip Number 2
Network with professionals in the Quality Assurance field, especially those who have experience in compliance roles. Engaging with them can provide insights into the company culture and expectations, which can be invaluable during interviews.
✨Tip Number 3
Prepare to discuss specific examples of how you've contributed to quality management systems in previous roles. Highlighting your hands-on experience with CAPAs, change controls, and audit readiness will set you apart from other candidates.
✨Tip Number 4
Showcase your communication skills by being clear and concise when discussing your experiences. As a Quality Assurance Compliance Manager, you'll need to engage with various stakeholders, so demonstrating your ability to communicate effectively is crucial.
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. Include specific examples of your work with validation and quality systems, as well as any relevant data integrity expertise.
Craft a Compelling Cover Letter: In your cover letter, emphasise your leadership skills and your ability to foster a compliance culture. Mention your experience with QMS compliance activities and how you can contribute to the Quality leadership team.
Showcase Relevant Skills: Clearly outline your communication and stakeholder engagement skills. Provide examples of how you've collaborated with different functions like QA, Manufacturing, and IT to meet regulatory expectations.
Highlight Continuous Improvement Initiatives: Discuss any past experiences where you led continuous improvement initiatives within a compliance framework. This will demonstrate your proactive approach to maintaining GxP standards and enhancing quality processes.
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 how you've implemented them in past positions. Highlight any training or initiatives you've led in this area.
✨Prepare for Cross-Functional Collaboration
This role requires collaboration with various teams. Think of examples where you've successfully worked with QA, Manufacturing, or IT to achieve compliance goals, and be ready to share these stories.
✨Demonstrate Leadership Skills
Since this is a leadership position, be prepared to discuss your experience in leading teams and driving a compliance culture. Share how you've motivated others to adhere to quality processes and continuous improvement.
