QA Manager

Hyper Recruitment Solutions Ltd; Keele; On-site; GBP 40,000 - 80,000; Full time

Job summary

An exciting opportunity awaits as a Quality Assurance Manager in a leading pharmaceutical company. This dynamic role involves overseeing Quality Assurance processes, ensuring compliance with Good Manufacturing Practices, and driving continuous improvement initiatives. As a key member of the Site Management Team, you will represent Quality Assurance interests and collaborate on local and global quality systems. If you're passionate about quality and looking to make a significant impact in the pharmaceutical sector, this role is perfect for you.

Qualifications

• Extensive experience in Quality Assurance, ideally within radiopharmaceuticals.
• Proven managerial experience with a strong performance track record.

Responsibilities

• Supervise Quality Assurance Officers and manage absence and overtime.
• Ensure compliance with maintenance schedules and perform audits.

Skills

Quality Assurance

GMP

Compliance

Audits

Continuous Improvement

Quality Systems

Quality Leadership

Quality Control

Education

Relevant degree in a scientific discipline

Tools

eQMS

LIMS

Job description

14520Permanent Competitive Site Based Keele, Staffordshire, United Kingdom Updated on: 17-04-2025

An exciting and dynamic role awaits as a Quality Assurance Manager within a leading pharmaceutical company based in the Staffordshire area. As the Quality Assurance Manager, you will be an active member of the Site Management Team, representing the interests of Quality Assurance and acting as the Quality Assurance lead on site. This role offers the chance to work with both local and global quality systems, ensuring compliance with Good Manufacturing Practice and promoting continuous improvement and consistency across the business.

KEY DUTIES AND RESPONSIBILITIES:

1. Supervise Quality Assurance Officers, Document Controller, and Admin and Quality Support Officer, managing absence, sickness, and overtime.
2. Support the introduction and development of an eQMS and/or LIMS system.
3. Participate in site/global projects as the QA expert and work with operational and project teams to develop and introduce new products.
4. Ensure compliance with maintenance schedules and perform internal and external audits as required.

ROLE REQUIREMENTS:

1. Relevant degree in a scientific discipline.
2. Extensive industry experience in Quality Assurance, ideally within radiopharmaceuticals.
3. Proven managerial or supervisory experience with a strong track record of performance.

Key Words: Quality Assurance / QA Manager / Pharmaceutical / Radiopharmaceuticals / GMP / eQMS / LIMS / Compliance / Audits / Continuous Improvement / Quality Systems / Site Management / Regulatory Compliance / Quality Leadership / Quality Control

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.