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- Tasks: Lead compliance activities and ensure adherence to GxP standards in a dynamic environment.
- Company: Join a leading pharmaceutical company dedicated 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: This role offers a chance to influence quality processes across the UK site and affiliates.
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 regulations that apply to 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 Quality Assurance field, especially those who have experience in GMP/GDP environments. Attend industry events or join relevant online forums to connect with potential colleagues and learn about best practices.
✨Tip Number 3
Prepare to discuss your experience with validation master plans and data integrity during interviews. Be ready to share specific examples of how you've contributed to compliance initiatives in previous roles.
✨Tip Number 4
Showcase your communication and stakeholder engagement skills by preparing scenarios where you've successfully collaborated with cross-functional teams. Highlighting these experiences can set you apart as a candidate who can lead and influence 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. 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 how your background aligns with the key responsibilities of the role, such as leading QMS compliance activities and your experience with data integrity.
Showcase Relevant Skills: Emphasise your communication and stakeholder engagement skills in your application. Provide examples of how you've collaborated with different teams to ensure compliance and improve quality processes.
Highlight Continuous Improvement Initiatives: Discuss any initiatives you've led or contributed to that focused on continuous improvement within quality management systems. This will show your proactive approach and commitment to maintaining high standards.
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. Think of scenarios where you improved data integrity and be ready to share those insights.
✨Highlight Cross-Functional Collaboration
This role requires collaboration with various teams. Prepare examples of how you've successfully worked with QA, Manufacturing, Validation, and IT functions to achieve compliance and improve quality processes.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world situations, such as handling CAPAs or audit readiness. Practise articulating your thought process and the steps you would take in these scenarios.
