We are currently looking for a Qualified Person to join a leading Pharmaceutical company based in the UK. As the Qualified Person, you will be responsible for ensuring the highest standards of quality and compliance in the production of radiopharmaceuticals.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Qualified Person will be varied however the key duties and responsibilities are as follows:
1. Overseeing the release of medicinal products for distribution, ensuring compliance with all relevant regulations and guidelines.
2. Reviewing and approving batch records, analytical data, and other documentation related to the manufacturing and testing of medicinal products.
3. Investigating and resolving quality issues and deviations related to manufacturing processes and materials.
4. Participating in internal and external audits of the manufacturing facilities and quality systems.
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 such as pharmacy, medicine, chemistry, pharmaceutical chemistry, or biology.
2. Proven industry experience in pharmaceutical manufacturing, quality assurance, and regulatory compliance.
3. A working knowledge and practical experience with Quality Management Systems and batch release processes.
Key Words:
Qualified Person / QP / Radiopharmaceuticals / Steriles / Quality Management System / Batch Release / Pharmaceutical Manufacturing / Regulatory Compliance / Quality Assurance / MHRA Licence
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.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Qualified Person will be varied however the key duties and responsibilities are as follows:
1. Overseeing the release of medicinal products for distribution, ensuring compliance with all relevant regulations and guidelines.
2. Reviewing and approving batch records, analytical data, and other documentation related to the manufacturing and testing of medicinal products.
3. Investigating and resolving quality issues and deviations related to manufacturing processes and materials.
4. Participating in internal and external audits of the manufacturing facilities and quality systems.
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 such as pharmacy, medicine, chemistry, pharmaceutical chemistry, or biology.
2. Proven industry experience in pharmaceutical manufacturing, quality assurance, and regulatory compliance.
3. A working knowledge and practical experience with Quality Management Systems and batch release processes.
Key Words:
Qualified Person / QP / Radiopharmaceuticals / Steriles / Quality Management System / Batch Release / Pharmaceutical Manufacturing / Regulatory Compliance / Quality Assurance / MHRA Licence
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.
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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