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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, professional growth opportunities, and potential remote work options.
- Why this job: Be a key player in fostering a strong compliance culture and making a real impact.
- Qualifications: Strong QA experience in pharmaceuticals, with expertise in data integrity and quality systems.
- Other info: Ideal for those passionate about quality assurance and regulatory compliance.
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 (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 quality assurance.
✨Tip Number 2
Network with professionals in the QA field, especially those who have experience in data integrity and compliance. Engaging with industry peers can provide valuable insights and may even lead to referrals for the position.
✨Tip Number 3
Prepare to discuss specific examples of how you've contributed to QMS compliance and continuous improvement in previous roles. Highlighting your hands-on experience will set you apart from other candidates.
✨Tip Number 4
Stay updated on the latest trends and technologies in quality assurance, particularly electronic quality systems like TrackWise and LIMS. Showing that you're proactive about learning can impress hiring managers.
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. 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.
Highlight Relevant Skills: Clearly outline your communication and stakeholder engagement skills. Provide examples of how you've successfully collaborated with cross-functional teams in previous roles, especially in relation to quality oversight and compliance.
Showcase Continuous Improvement Initiatives: Discuss any initiatives you've led or contributed to that focused on continuous improvement within quality processes. This could include your role in developing validation master plans or preparing for audits.
How to prepare for a job interview at Nexia Life Sciences
✨Showcase Your Compliance Knowledge
Make sure to highlight your understanding of GxP standards and how they apply to Quality Management Systems. Be prepared to discuss specific examples from your past experience where you ensured compliance and improved processes.
✨Demonstrate Leadership Skills
As this role is a leadership position, it's crucial to convey your ability to lead teams effectively. Share instances where you've successfully guided teams through compliance challenges or implemented quality initiatives.
✨Prepare for Technical Questions
Expect questions related to validation, CAPA, and data integrity. Brush up on these topics and be ready to explain your approach to maintaining compliance and managing quality systems in a regulated environment.
✨Engage with Stakeholders
Since stakeholder engagement is key, prepare to discuss how you've collaborated with different departments in the past. Highlight your communication skills and provide examples of how you've built strong relationships to drive compliance efforts.
