Quality Assurance Manager

RBW Consulting LLP; Manchester; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading pharmaceutical company in Greater Manchester seeks a Quality Assurance Manager to oversee QA activities and compliance with GMP. The role requires a strong background in pharmaceuticals and the ability to mentor staff and lead QA initiatives. This position offers an opportunity to make a lasting impact in a growing environment.

Qualifications

• Minimum 5 years experience in Quality Assurance, ideally within steriles.
• Previous managerial or supervisory experience with proven leadership skills.
• Strong understanding of contamination control strategies and data integrity principles.

Responsibilities

• Lead site QA activities and represent QA in the Site Management Team.
• Oversee internal and external audits, deviations, CAPAs, change controls, and investigations.
• Drive continuous improvement and support globalization of SOPs and quality systems.

Skills

Leadership

Regulatory knowledge (GMP, MHRA, HSE)

Communication skills

Organizational skills

Interpersonal skills

Proficiency in Microsoft Office

Education

Degree or equivalent in a relevant scientific discipline

Tools

PrOFS

Job description

Quality Assurance Manager Greater Manchester

Were working with a leading pharmaceutical company entering an exciting phase of growth, with new product introductions, operational scale-ups, and expansions at their brand-new site. This is a unique opportunity to join a small, hands‑on site where youll play a key leadership role in shaping its QA function.

As QA Manager, youll manage operational and project teams to ensure compliance with GMP, support product development, and maintain inspection readiness. Youll also play a key role in implementing digital systems like eQMS and LIMS and contribute to global quality initiatives.

This is a fantastic opportunity for a quality professional with a strong background in pharmaceuticals who is ready to lead, mentor, and make a lasting impact.

Key Responsibilities

• Lead site QA activities and represent QA in the Site Management Team.
• Oversee internal and external audits, deviations, CAPAs, change controls, and OOS / OOT investigations.
• Maintain contamination control strategy and ensure Data Integrity principles are upheld.
• Drive continuous improvement and support globalisation of SOPs and quality systems.
• Manage and mentor QA staff, ensuring training and development plans are in place.
• Support regulatory inspections (MHRA, HSE) and ensure compliance with licenses and GMP.
• Collaborate on new product development and system implementations (eQMS / LIMS).

Requirements

• Degree or equivalent in a relevant scientific discipline.
• Minimum 5 years experience in Quality Assurance, ideally within steriles.
• Previous managerial or supervisory experience with proven leadership skills.
• Strong regulatory knowledge (GMP, MHRA, HSE).
• Excellent communication, organisation, and interpersonal skills.
• Proficiency in Microsoft Office and understanding of PrOFS.