RA QA Manager

Meet Recruitment; Bracknell; On-site; GBP 45,000 - 55,000; Full time

Job summary

A leading company in the Biotech/Pharmaceuticals sector is seeking an experienced RA QA Manager in Bracknell. The ideal candidate will manage regulatory submissions, ensure compliance with regulations, and lead quality audits. With a bachelor's degree and over 5 years of experience required, you'll play a crucial role in driving compliance and quality strategies within a dynamic team. This permanent position offers a salary between £45,000 and £55,000, depending on experience.

Qualifications

• 5+ years of experience in regulatory affairs and quality assurance.
• Strong understanding of regulatory requirements in the biotech/pharmaceutical industry.
• Experience with regulatory submissions and audits.

Responsibilities

• Manage regulatory submissions and approvals.
• Ensure compliance with relevant regulations and guidelines.
• Lead quality audits and inspections.
• Support product development teams in regulatory strategy.
• Drive continuous improvement in quality processes.

Skills

Regulatory submissions and approvals

Quality audits and inspections

Continuous improvement in quality processes

Collaborating with cross‑functional teams

Strong understanding of regulatory requirements

Education

Bachelor's degree in a related field

Job description

RA QA Manager

170119 Posted : 07 / 07 / 2025

• 45000 GBP - 55000 GBP
• Bracknell, United Kingdom
• Permanent

Our client, a leading company in the Biotech / Pharmaceuticals sector, is at the forefront of innovation and development. They are currently in search of a skilled and experienced RA QA Manager to join their expanding team. This position presents a fantastic opportunity to have a considerable impact within the organization and play a pivotal role in shaping the future of the industry.

Role Summary :

As the RA QA Manager, you will oversee all regulatory affairs and quality assurance activities within the company. Collaborating with cross‑functional teams, you will ensure compliance with regulatory requirements and quality standards. This role can be based either onsite at our client's Berkshire location.

Key Responsibilities :

• Manage regulatory submissions and approvals
• Ensure compliance with relevant regulations and guidelines
• Lead quality audits and inspections
• Support product development teams in regulatory strategy
• Drive continuous improvement in quality processes

Experience & Requirements :

• Bachelor's degree in a related field
• 5+ years of experience in regulatory affairs and quality assurance
• Strong understanding of regulatory requirements in the biotech / pharmaceutical industry
• Experience with regulatory submissions and audits
• Certification in regulatory affairs is a plus

This role offers a base salary ranging between £45,000 and £55,000, dependent on experience.

Apply now to join a growing team that is shaping the future of the Biotech / Pharmaceuticals sector.

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