2 days ago Be among the first 25 applicants
Duration: 12-Month Contract (Inside IR35)
Location: Halton, UK
About the Role
Our client is seeking an experienced Qualified Person (QP) to join their team on a 12-month contract. You’ll play a critical role in ensuring that all products released to market meet the highest standards of compliance and quality, in line with EU, USA, and global regulatory requirements.
Key Responsibilities
- Perform final QP batch certification for market release.
- Ensure compliance with cGMP principles and regulatory requirements.
- Review and certify batches according to shipment schedules.
- Verify documentation and support change control processes.
What We’re Looking For
- Degree in Science or equivalent.
- Registered Qualified Person, recognised by the Licensing Authority.
- Strong experience in pharmaceutical manufacturing and quality leadership.
- Excellent communication and influencing skills.
Why Join?
This is a fantastic opportunity to make an impact in a leading pharmaceutical environment, ensuring patient safety and regulatory excellence.
Apply Today
If you’re a proactive QP ready for your next challenge, we’d love to hear from you.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Quality Assurance
Industries
Pharmaceutical Manufacturing and Biotechnology Research
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Contact Detail:
i-Pharm Consulting Recruiting Team