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A leading company in the pharmaceutical industry is seeking a Qualified Person (QP) to join their team in the Oxford area. As a Qualified Person, you will play a crucial role in ensuring that each batch of product is manufactured and checked in compliance with UK and EU regulations, GMP and relevant marketing authorisations.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Qualified Person will be varied however the key duties and responsibilities are as follows:
1. Ensure certification of batches under the terms of the manufacturer's importation authorisation.
2. Assess each batch for certification prior to release, including reviewing batch records, QC data, and all relevant documents.
3. Confirm that all manufacturing and quality control activities comply with GMP principles.
4. Oversee the pharmaceutical quality systems to ensure product safety and data reliability.
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 history:
1. Currently operating as a QP with proven industry experience withing a Biologics pharmaceutical business.
2. Relevant experience working within a Sterile environment.
3. A working knowledge and practical experience with EU and UK GMP regulations.
Key Words:
Qualified Person / QP / GMP / Advanced Therapy Medicinal Products/ ATMP/ Sterile
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 in the Oxford area. As a Qualified Person, you will play a crucial role in ensuring that each batch of product is manufactured and checked in compliance with UK and EU regulations, GMP and relevant marketing authorisations.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Qualified Person will be varied however the key duties and responsibilities are as follows:
1. Ensure certification of batches under the terms of the manufacturer's importation authorisation.
2. Assess each batch for certification prior to release, including reviewing batch records, QC data, and all relevant documents.
3. Confirm that all manufacturing and quality control activities comply with GMP principles.
4. Oversee the pharmaceutical quality systems to ensure product safety and data reliability.
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 history:
1. Currently operating as a QP with proven industry experience withing a Biologics pharmaceutical business.
2. Relevant experience working within a Sterile environment.
3. A working knowledge and practical experience with EU and UK GMP regulations.
Key Words:
Qualified Person / QP / GMP / Advanced Therapy Medicinal Products/ ATMP/ Sterile
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.
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