Back to Job SearchROLE OVERVIEW
A leading company in the pharmaceutical industry is seeking a Qualified Person (QP) to join their team based in Oxfordshire. As the Qualified Person, you will play a pivotal role in ensuring that each batch of product is manufactured and checked in compliance with UK and EU regulations, adhering to Good Manufacturing Practice (GMP) standards.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Qualified Person will be varied however the key duties and responsibilities are as follows:
1. Certify that each batch of product meets all regulatory and GMP requirements before release to the market or for export.
2. Ensure all manufacturing and quality control activities are conducted according to GMP principles.
3. Maintain comprehensive documentation of the full supply chain for each product.
4. Oversee batch review and disposition of clinical and commercial products for use in the EU and UK.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Qualified Person we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific discipline.
2. Proven industry experience in pharmaceutical manufacturing and quality control (ideally experience with ATMPs.)
3. A working knowledge and practical experience with EU and UK GMP regulations.
Key Words:
Qualified Person / QP / pharmaceutical manufacturing / GMP / batch release / quality control / clinical trials / regulatory compliance / pharmaceutical industry / Advanced Therapy Medicinal Products / ATMP
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
A leading company in the pharmaceutical industry is seeking a Qualified Person (QP) to join their team based in Oxfordshire. As the Qualified Person, you will play a pivotal role in ensuring that each batch of product is manufactured and checked in compliance with UK and EU regulations, adhering to Good Manufacturing Practice (GMP) standards.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Qualified Person will be varied however the key duties and responsibilities are as follows:
1. Certify that each batch of product meets all regulatory and GMP requirements before release to the market or for export.
2. Ensure all manufacturing and quality control activities are conducted according to GMP principles.
3. Maintain comprehensive documentation of the full supply chain for each product.
4. Oversee batch review and disposition of clinical and commercial products for use in the EU and UK.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Qualified Person we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific discipline.
2. Proven industry experience in pharmaceutical manufacturing and quality control (ideally experience with ATMPs.)
3. A working knowledge and practical experience with EU and UK GMP regulations.
Key Words:
Qualified Person / QP / pharmaceutical manufacturing / GMP / batch release / quality control / clinical trials / regulatory compliance / pharmaceutical industry / Advanced Therapy Medicinal Products / ATMP
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Your Recruitment Consultant
Share this Job
