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QA Specialist

ROLE OVERVIEW

We are currently looking for a QA Specialist to join a leading nuclear medicine company to cover Maternity Leave on an FTC basis. As the QA Specialist, you will be responsible for ensuring the highest standards of quality and compliance in the production and testing of radiopharmaceuticals.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the QA Specialist will be varied; however, the key duties and responsibilities are as follows:

1. Reviewing compliance of production and analytical methods with GMP guidelines and relevant pharmacopoeias.

2. Managing documentation, including reviewing and updating SOPs, forms, and quality records.

3. Assisting with the review and approval of deviations, incidents, investigations, and CAPA.

4. Performing and reviewing QC tests, managing out-of-specification results, and ensuring timely completion of quality records.

ROLE REQUIREMENTS:

To be successful in your application to this exciting role as the QA Specialist, 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 quality control within radiopharmacy.

3. A working knowledge and practical experience with GMP and pharmaceutical chemistry.

Key Words: QA Specialist / Quality Assurance / Radiopharmacy / GMP / QC Testing / SOPs / CAPA / Pharmaceutical Chemistry / Compliance / Documentation Management / London UCLH Hospital

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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