At a Glance
- Tasks: Ensure quality and compliance in pharmaceutical manufacturing by certifying batches and overseeing GMP activities.
- Company: Established pharmaceutical site with a focus on quality and regulatory excellence.
- Benefits: Competitive pay, hands-on experience, and potential for long-term contracts.
- Other info: On-site role with flexible part-time options available.
- Why this job: Join a dynamic team and make a real impact in the pharmaceutical industry.
- Qualifications: Must be an eligible QP with significant experience in sterile manufacturing.
The predicted salary is between 59400 - 72600 £ per year.
An established pharmaceutical manufacturing site is seeking an experienced Qualified Person (QP) to support batch release for commercial and clinical products. This is a hands-on contracting role requiring a strong understanding of UK and EU GMP requirements, Annex 16, and quality leadership within a regulated manufacturing environment.
Key Responsibilities:
- Act as a named QP on the site MIA and IMP licences.
- Perform batch certification and release of commercial and clinical products in line with UK/EU GMP and Annex 16.
- Confirm compliance of manufacturing steps either directly or through agreed delegation.
- Provide QP oversight of GMP activities across manufacturing, packaging, and testing.
- Support disposition of intermediates and finished products.
- Provide quality input into deviations, OOS, change controls, and CAPAs.
- Review and approve GMP documentation and operational procedures.
Required Experience & Qualifications:
- Eligible to act as a QP under UK/EU regulations.
- Significant pharmaceutical manufacturing experience, ideally including sterile and/or biological products/sterile manufacturing.
- Proven experience with Annex 16 batch certification.
About the role:
On-site presence is required for 5 days, and we would consider 2 part-time FTEs. Suitable for experienced QP contractors seeking a technically solid site with long-term potential.
Please click "apply now" to send an updated CV to Julia Bowden at Hays.
QP Contract Outside IR35 - Sterile in Cheshire employer: Hays Specialist Recruitment Limited Careers
Hays Education is an exceptional employer, offering a supportive and collaborative work environment for SEN SLD/PMLD teachers in the Hounslow/Hillingdon area. With access to exclusive vacancies, ongoing professional development, and a dedicated consultant to guide your career, you will find ample opportunities for growth while making a meaningful impact on the lives of pupils with special educational needs. Join us to be part of a community that values inclusivity and fosters both personal and professional development.
Contact Details:
Hays Specialist Recruitment Limited Careers Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land QP Contract Outside IR35 - Sterile in Cheshire
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We think you need these skills to ace QP Contract Outside IR35 - Sterile in Cheshire
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Hays Specialist Recruitment Limited Careers!
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Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Hays Specialist Recruitment Limited Careers, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Hays Specialist Recruitment Limited Careers
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Hays Specialist Recruitment Limited Careers that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
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