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Quality Assurance Officer
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Birmingham |🏠Fully Onsite | Permanent
Looking to build your career in Pharmaceutical Quality Assurance?
We're partnering with an established pharmaceutical manufacturer that's investing in its Quality function and is looking for a Quality Assurance Officer to join its Birmingham site.
This is a fantastic opportunity to become part of a business operating within a highly regulated GMP environment, where you'll gain exposure across manufacturing, quality systems, compliance and continuous improvement while working alongside an experienced Quality leadership team. If you enjoy variety, thrive in a fast-paced manufacturing environment and want a role where your work genuinely impacts patient outcomes, we'd love to hear from you.
The Opportunity:
As a Quality Assurance Officer, you'll play a central role in maintaining GMP compliance across site operations. You'll work closely with Manufacturing, QC and Supply Chain teams to ensure products are manufactured to the highest quality standards:
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Your responsibilities will include:
- Reviewing batch manufacturing and packaging records
- Supporting deviation investigations, CAPAs and change controls
- Maintaining GMP documentation, SOPs and Quality Management Systems (QMS)
- Providing QA oversight across manufacturing operations
- Supporting internal audits, supplier audits and regulatory inspections
- Monitoring quality metrics and identifying opportunities for continuous improvement
- Promoting a strong quality culture across the business
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About you:
You'll ideally have:
- Previous Quality Assurance experience within pharmaceutical manufacturing
- Strong knowledge of GMP regulations and pharmaceutical quality systems
- Experience reviewing batch documentation
- Hands-on experience with deviations, CAPAs, change controls and document control
- Excellent attention to detail and organisational skills
- The ability to build strong working relationships across multiple departments
Desirable
- Experience within specialist pharmaceutical manufacturing
- Exposure to MHRA inspections or audit preparation
- Experience supporting highly regulated manufacturing environments
- Knowledge of controlled products or complex pharmaceutical supply chains
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