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For Companies At a Glance
- Tasks: Review clinical batch records and conduct audits to ensure compliance.
- Company: Join a global healthcare leader with a diverse portfolio of medicines and vaccines.
- Benefits: Enjoy flexible working with home options and competitive pay from £20.00 - £26.00 per hour.
- Why this job: Be part of a mission-driven company that impacts global health and patient care.
- Qualifications: A relevant scientific degree or equivalent experience in QA within a GMP environment is required.
- Other info: This role involves one or two days in London, with the rest remote.
CK Group are recruiting for a Quality Auditor to join a biopharmaceutical company on a contract basis for 6 months.
Salary: From £20.00 - £26.00 per hour PAYE, depending upon experience.
Quality Auditor Role:
- Be responsible for the final review of clinical batch records.
- Compilation and approval of data packs and presentation to the QP for final release.
- Conduct routine audits of data, information, procedures, equipment and systems.
- Review and approve production and analytical documentation accompanying the release of API, Safety Assessment or clinical supply lots.
- Perform audits or inspections of assigned areas or systems to assess compliance with regulatory and Company standards.
Your Background:
- Hold a relevant scientific degree or have equivalent working experience.
- Experience in a QA or similar role in a GMP environment.
- Previous experience in the pharmaceutical industry.
- Good knowledge of GMP standards and requirements.
- Experience in audit procedures would be an advantage but the client may also be interested in candidates with QA background with no audit experience.
Company: Our client is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. They have an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe.
Location: This role is based at our client's site in London for one or two days per week, with the rest home working.
Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 136 692 in all correspondence. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
If this position isn’t suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Quality Auditor employer: CK Group
Contact Detail:
CK Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Auditor
✨Tip Number 1
Familiarise yourself with GMP standards and regulations, as this role heavily relies on compliance. Brush up on your knowledge of these guidelines to demonstrate your understanding during any discussions.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those in QA roles. Engaging with them can provide insights into the company culture and expectations, which can be invaluable during interviews.
✨Tip Number 3
Prepare to discuss your previous experiences in quality assurance or related fields. Be ready to share specific examples of how you've ensured compliance and improved processes in past roles.
✨Tip Number 4
Research the biopharmaceutical company you're applying to. Understanding their products and values will help you tailor your conversation and show genuine interest in their mission during the interview.
We think you need these skills to ace Quality Auditor
Some tips for your application 🫡
Understand the Role: Read the job description carefully to understand the responsibilities and requirements of the Quality Auditor position. Tailor your application to highlight relevant experience in QA and GMP environments.
Highlight Relevant Experience: In your CV and cover letter, emphasise any previous roles in quality assurance or similar positions, especially within the pharmaceutical industry. Mention specific examples of your experience with audits, compliance, and documentation.
Showcase Your Qualifications: Make sure to include your scientific degree or equivalent experience prominently in your application. If you have certifications related to GMP or quality auditing, mention these as well.
Follow Application Instructions: When applying, ensure you quote the job reference 136 692 in all correspondence. This shows attention to detail and helps the employer track your application.
How to prepare for a job interview at CK Group
✨Know Your GMP Standards
Make sure you have a solid understanding of Good Manufacturing Practice (GMP) standards. Be prepared to discuss how these standards apply to your previous roles and how you ensure compliance in your work.
✨Showcase Your Audit Experience
Even if you don't have direct audit experience, highlight any relevant QA experience. Discuss specific situations where you ensured quality and compliance, and be ready to explain your approach to problem-solving in those scenarios.
✨Prepare for Technical Questions
Expect technical questions related to clinical batch records and data pack compilation. Brush up on your knowledge of the processes involved and be ready to explain them clearly and confidently.
✨Demonstrate Your Communication Skills
As a Quality Auditor, you'll need to communicate effectively with various teams. Prepare examples of how you've successfully collaborated with others in the past, especially in high-pressure situations.
