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An exciting role has arisen for a Quality Assurance Associate to join a leading pharmaceutical company based in the Slough area. As the Quality Assurance Specialist, you will be responsible for ensuring site operations performance by managing and supporting GMP issues through QMS processes, site governance, and senior QA leadership.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Quality Assurance Specialist will be varied; however, the key duties and responsibilities are as follows:
1. Provide shoulder-to-shoulder review of documentation generated during manufacturing, development, and laboratory processes.
2. Advise on best practices for document completion, review, and follow-up actions, escalating if required.
3. Act as a point of contact for general queries relating to Quality, escalating as necessary.
4. Identify and report non-conformances, resolving issues through interaction with relevant personnel.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Quality Assurance Associate, we are looking to identify the following on your profile and past history:
1. Relevant degree in Field Study Biology or a related field.
2. Proven industry experience in Quality Assurance, GMP and data entry.
3. A working knowledge and practical experience with PQS/QMS and GMP auditing.
Key Words:
Quality Assurance / GMP / QMS / Pharmaceutical / Compliance / Documentation Review / Continuous Improvement / Audit Readiness / Regulatory Standards / Quality Processes / Risk-Based Decision Making
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.
An exciting role has arisen for a Quality Assurance Associate to join a leading pharmaceutical company based in the Slough area. As the Quality Assurance Specialist, you will be responsible for ensuring site operations performance by managing and supporting GMP issues through QMS processes, site governance, and senior QA leadership.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Quality Assurance Specialist will be varied; however, the key duties and responsibilities are as follows:
1. Provide shoulder-to-shoulder review of documentation generated during manufacturing, development, and laboratory processes.
2. Advise on best practices for document completion, review, and follow-up actions, escalating if required.
3. Act as a point of contact for general queries relating to Quality, escalating as necessary.
4. Identify and report non-conformances, resolving issues through interaction with relevant personnel.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Quality Assurance Associate, we are looking to identify the following on your profile and past history:
1. Relevant degree in Field Study Biology or a related field.
2. Proven industry experience in Quality Assurance, GMP and data entry.
3. A working knowledge and practical experience with PQS/QMS and GMP auditing.
Key Words:
Quality Assurance / GMP / QMS / Pharmaceutical / Compliance / Documentation Review / Continuous Improvement / Audit Readiness / Regulatory Standards / Quality Processes / Risk-Based Decision Making
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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