QP - Full Time Contract Outside IR35
other jobs Hays Specialist Recruitment Limited
Added before 2 Days
- England,North West,Cheshire,Cheshire West and Chester
- Full Time, Contract
- £1,000 - £1,150 per day
Job Description:
Your Company
An established pharmaceutical manufacturing site is seeking an experienced Qualified Person (QP) to support batch certification and quality operations 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:
QP & Batch Certification
*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.
Quality Operations & Oversight
*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 required for 5 days
*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.
An established pharmaceutical manufacturing site is seeking an experienced Qualified Person (QP) to support batch certification and quality operations 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:
QP & Batch Certification
*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.
Quality Operations & Oversight
*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 required for 5 days
*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.
Job number 3328481
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Company Details:
Hays Specialist Recruitment Limited
At Hays we invest in lifelong partnerships that empower people and businesses to succeed. With over 50 years? success under our belts and a workforce ...