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- Tasks: Conduct audits and enhance quality standards in a dynamic environment.
- Company: Join Resolian, a leader in quality assurance for medical devices.
- Benefits: Competitive salary, professional development, and a collaborative team culture.
- Why this job: Make a real impact on quality management in the healthcare industry.
- Qualifications: Experience in QA processes and strong knowledge of GLP and GCP regulations.
- Other info: Opportunity for continuous improvement and career growth in a supportive team.
The predicted salary is between 40000 - 50000 £ per year.
Conduct study, process, and facility audits according to the audit programme and study timelines in accordance with GLP and GCP requirements.
Collaborate with QA and Operational teams across Resolian to enhance quality standards, streamline processes, and drive operational efficiencies.
Where required, lead the planning and implementation of quality management systems for IVD medical devices.
Maintain strong and up‑to‑date knowledge of applicable regulations, standards, and industry guidance.
Provide expert advice and interpretation of regulatory requirements.
Support the maintenance and continual improvement of Quality Management Systems (QMS).
Support external inspections, customer audits, and customer enquiries.
Contribute to the delivery and improvement of training modules.
Identify, propose, and drive continuous improvement initiatives.
Support the internal self‑inspection programme.
Assist with deviation and Quality Incident investigations.
Participate in external sponsor audits, ensuring feedback is captured and fed into process improvements.
Build and maintain effective working relationships with suppliers, acting as a key point of contact for external communications.
QA Advisor/ Sr. QA Advisor (GLP & GCP) employer: Resolian
Contact Detail:
Resolian Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QA Advisor/ Sr. QA Advisor (GLP & GCP)
✨Tip Number 1
Network like a pro! Reach out to professionals in the QA field on LinkedIn or at industry events. Building connections can lead to job opportunities that aren’t even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on GLP and GCP regulations. We recommend creating a cheat sheet of key points to discuss, so you can showcase your expertise and confidence during the interview.
✨Tip Number 3
Don’t just wait for job openings; be proactive! Reach out to companies you admire, like Resolian, and express your interest in potential QA roles. Sometimes, they might create a position just for you!
✨Tip Number 4
Keep your skills sharp! Consider taking online courses related to quality management systems or regulatory requirements. This not only boosts your CV but also shows employers that you’re committed to continuous improvement.
We think you need these skills to ace QA Advisor/ Sr. QA Advisor (GLP & GCP)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the QA Advisor role. Highlight your experience with GLP and GCP, and don’t forget to mention any relevant audits or quality management systems you've worked with. We want to see how your skills align with what we’re looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about quality assurance and how you can contribute to our team. Be specific about your experiences and how they relate to the job description. We love a good story!
Showcase Your Knowledge: We’re keen on candidates who stay up-to-date with industry regulations and standards. In your application, mention any recent training or certifications you’ve completed that relate to QA. This shows us you’re proactive and committed to continuous improvement.
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it gives you a chance to explore more about StudySmarter and what we stand for!
How to prepare for a job interview at Resolian
✨Know Your GLP & GCP Inside Out
Make sure you brush up on Good Laboratory Practice (GLP) and Good Clinical Practice (GCP) regulations. Be prepared to discuss how these standards apply to the role and share examples of how you've implemented them in past positions.
✨Showcase Your Collaboration Skills
Since the role involves working with QA and Operational teams, think of specific instances where you've successfully collaborated with others. Highlight your ability to enhance quality standards and streamline processes through teamwork.
✨Be Ready for Scenario-Based Questions
Expect questions that ask how you would handle audits or quality incidents. Prepare by thinking through potential scenarios and your approach to resolving issues while maintaining compliance with regulations.
✨Demonstrate Continuous Improvement Mindset
The company values continuous improvement initiatives, so come prepared with ideas or examples of how you've driven improvements in previous roles. This shows you're proactive and committed to enhancing quality management systems.