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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 competitive pay, flexible working options, and professional development opportunities.
- Why this job: Be part of a dynamic team shaping a strong compliance culture with real impact.
- Qualifications: Experience in pharmaceutical QA and familiarity with quality systems required.
- Other info: Opportunity to collaborate across departments and enhance your leadership skills.
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
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 in interviews but also demonstrate your commitment to compliance and quality management.
✨Tip Number 2
Network with professionals in the QA and compliance field, especially those who have experience in pharmaceutical settings. Attend industry conferences or webinars to connect with potential colleagues and learn about best practices in quality management.
✨Tip Number 3
Prepare to discuss specific examples of how you've contributed to quality improvement initiatives in previous roles. Highlight your experience with CAPAs, change controls, and audit readiness to showcase your expertise.
✨Tip Number 4
Research StudySmarter's values and culture, and think about how your personal values align with them. Being able to articulate this connection during your discussions can set you apart as a candidate who is not only qualified but also a good cultural fit.
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, express your passion for quality assurance and compliance. Mention your experience with data integrity and how you can contribute to building a strong compliance culture at the company.
Highlight Relevant Skills: Emphasise your communication and stakeholder engagement skills, as these are crucial for the role. Provide examples of how you've successfully collaborated with cross-functional teams in the past.
Showcase Continuous Improvement Initiatives: Discuss any initiatives you've led or contributed to that focused on continuous improvement within quality management systems. This will demonstrate your proactive approach to compliance and 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. Share your experiences in educating teams on maintaining data integrity and how it impacts overall quality.
✨Highlight Your Leadership Skills
This role is about leading compliance activities, so demonstrate your leadership experience. Talk about how you've driven continuous improvement initiatives and built a compliance culture in past positions.
✨Prepare for Cross-Functional Collaboration
Collaboration is key in this role. Be ready to discuss how you've worked with various departments like QA, Manufacturing, and IT to ensure regulatory compliance. Provide examples of successful projects that required teamwork.
