QA Associate

We are recruiting a QA Associate to join a leading Pharmaceutical company based in the Berkshire area. As the QA Associate, you will play a crucial role in ensuring quality and compliance within the QA Operations Documentation Control Team.

This is an initial 9 month contract with possible extension thereafter.


KEY DUTIES AND RESPONSIBILITIES:

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

1. As the QA Associate, you will perform Batch Consolidation duties related to QC Biochemistry and Microbiology testing activities for Drug Product and Drug Substance.

2. As the QA Associate, you will liaise with internal customers to ensure receipt of required information and maintain effective interdepartmental communication and collaboration.

3. As the QA Associate, you will assist with preparatory work prior to audits and provide QC consolidated related information during customer and regulatory audits.

4. As the QA Associate, you will issue approved GMP documents and labels to Manufacturing, ensuring deadlines are met.


ROLE REQUIREMENTS:

To be successful in your application to this exciting role as the QA Associate, we are looking to identify the following on your profile and past history:

1. Relevant degree in Biology or a related field.

2. Proven industry experience in QA or GMP environments.

3. A working knowledge and practical experience with quality procedures and data entry.

Key Words: QA Associate / Quality Assurance / Batch Consolidation / GMP / QC Biochemistry / QC Microbiology / Drug Product / Drug Substance / Documentation Control / Pharmaceutical Industry / Berkshire

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.