Senior Quality Assurance Officer

RBW Consulting; England; On-site; GBP 35,000 - 50,000; Full time

Job summary

A leading pharmaceutical consulting firm is seeking a Senior QA Officer in Wiltshire. The role includes managing daily quality assurance activities, coaching junior staff, and ensuring high standards in a compliance-focused environment. This position offers a chance to significantly impact pharmaceutical product safety and quality.

Qualifications

• 2-4 years of QA experience within a GMP-regulated environment.
• Strong working knowledge of pharmaceutical quality systems.
• Experience working cross-functionally with QA/QC teams.

Responsibilities

• Support the QA Manager in day-to-day quality assurance activities.
• Coach and support junior team members.
• Contribute to audit readiness and maintain quality systems.

Skills

GMP knowledge

Quality systems

Coaching

Continuous improvement

Job description

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Senior QA Officer – Pharmaceutical Manufacturing – Wiltshire (On-site)

I am partnered exclusively with a well-established and rapidly growing pharmaceutical CDMO that continues to invest in innovation, quality, and expansion across the UK.

This hire will play a key role in supporting the QA Manager by taking ownership of day-to-day quality assurance activities and contributing to the development of the wider QA function. You’ll be working closely with manufacturing and QC teams, helping to drive compliance, training, and continuous improvement across the site.

This is a hands-on QA role where your experience in GMP environments will be essential. You’ll be expected to coach and support junior team members, contribute to audit readiness, and ensure that quality systems are maintained to the highest standards.

If you’re looking for a role where your work directly impacts the safety and quality of pharmaceutical products – and where your contributions are visible and valued, this is a fantastic opportunity to grow within a collaborative, agile, and innovation-driven environment.

Key experience:

• 2-4 years of QA experience within a GMP-regulated pharmaceutical environment
• Strong working knowledge of GMP and pharmaceutical quality systems
• Experience working cross-functionally with QA/QC and operational teams
• Confident in coaching, training, and supporting junior staff
• A proactive mindset with a passion for continuous improvement

If you’re interested in joining a company where you’re not just a number and where you’ll gain exposure to a wide variety of projects and clients - please apply.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Pharmaceutical Manufacturing

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Wiltshire, England, United Kingdom 2 weeks ago

Wiltshire, England, United Kingdom 2 weeks ago

Wiltshire, England, United Kingdom 2 weeks ago

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