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- Tasks: Lead compliance activities and ensure quality management systems meet GxP standards.
- Company: Join a leading pharmaceutical company dedicated to quality and compliance.
- Benefits: Enjoy a collaborative work environment with opportunities for continuous improvement and professional growth.
- Why this job: Be part of a dynamic team shaping a strong 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 like TrackWise or LIMS is a plus.
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
Locations
Quality Assurance Compliance Manager (Guildford) 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 (Guildford)
✨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 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 preparations to showcase your expertise.
✨Tip Number 4
Research StudySmarter's values and culture to align your approach during the interview process. Understanding our mission and how you can contribute to building a strong compliance culture will set you apart from other candidates.
We think you need these skills to ace Quality Assurance Compliance Manager (Guildford)
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 compliance activities or worked with quality management systems.
Craft a Strong Cover Letter: In your cover letter, address how your background aligns with the key responsibilities of the Quality Assurance Compliance Manager role. Mention specific examples of your experience with data integrity and compliance in regulated environments.
Highlight Relevant Skills: Clearly outline your skills related to validation, quality systems, and stakeholder engagement. Use bullet points to make these stand out, ensuring they match the requirements listed in the job description.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a role focused on compliance.
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.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world situations, such as handling CAPAs or audit readiness. Think of examples where you've successfully navigated challenges in quality assurance.
✨Demonstrate Cross-Functional Collaboration
This role requires working closely with various departments. Be prepared to discuss how you've effectively collaborated with QA, Manufacturing, Validation, and IT teams to achieve compliance and improve processes.
