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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 with opportunities for continuous improvement and professional growth.
- Why this job: Be part of a dynamic team shaping compliance culture and making a real impact.
- Qualifications: Strong QA experience in pharmaceuticals, especially in GMP/GDP and data integrity.
- Other info: Familiarity with electronic quality systems is a plus.
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
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 quality assurance.
✨Tip Number 2
Network with professionals in the QA field, especially those who have experience in compliance roles. Attend industry events or join online forums to connect with others and gain insights into best practices and current trends.
✨Tip Number 3
Prepare to discuss specific examples of how you've contributed to quality management systems in previous roles. Highlight your experience with CAPAs, change controls, and audit readiness to showcase your expertise.
✨Tip Number 4
Research StudySmarter's approach to quality assurance and compliance. Understanding our values and how we implement quality processes can give you an edge in demonstrating your alignment with our goals during the interview.
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 to demonstrate your 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 data integrity and how you can contribute to the Quality leadership team.
Showcase Relevant Skills: Clearly outline your skills related to QMS compliance activities, stakeholder engagement, and familiarity with electronic quality systems like TrackWise or LIMS. Use bullet points for clarity.
Proofread Your Application: Before submitting, carefully proofread your application for any errors or inconsistencies. A well-presented application reflects your attention to detail, which is crucial for a role in quality assurance.
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. Think of scenarios where you successfully advised teams on maintaining data integrity.
✨Highlight Your Leadership Skills
This role is about leading compliance activities, so be sure to share your experiences in leading teams or projects. Discuss how you foster a culture of compliance and continuous improvement.
✨Prepare for Cross-Functional Collaboration
Collaboration is key in this role. Be ready to talk about how you've worked with different departments like QA, Manufacturing, and IT to ensure regulatory compliance. Specific examples will help illustrate your teamwork skills.
