Quality Assurance Specialist

Quality Assurance Engineer/Specialist – Alton – Office Based

I am currently working with a leading CDMO manufacturing business based in Alton, supporting the pharmaceutical, medical device, cosmetics, and nutritional sectors. This is an excellent opportunity for an experienced Quality Assurance professional to join a fast-paced environment and contribute to ensuring compliance across production and customer operations.

Key responsibilities for the Quality Assurance Engineer/Specialist

• Coordinate and manage the internal audit programme, including planning, execution, reporting, and follow-up of corrective actions.
• Lead investigations into non-conformities and quality issues, applying problem-solving techniques to identify root causes and implement effective CAPAs.
• Manage the Change Control process to ensure regulatory and operational compliance.
• Investigate customer quality issues and consumer complaints, providing timely responses and corrective actions.
• Review and complete deviations, allocating actions to relevant teams and ensuring closure.
• Support new product introduction projects, including line trials, capability studies, and product inspections to meet customer specifications.
• Oversee QA validation team operations, including workload allocation and performance reviews.
• Review and sign off packing specifications and support with PQR reporting.
• Liaise with customers and attend meetings to represent the QA function.

Requirements for the Quality Assurance Engineer/Specialist

• Qualified and experienced internal auditor.
• Strong background in Quality Assurance within GMP-regulated environments (pharma, medical device, cosmetics).
• Good knowledge of quality improvement tools and problem-solving techniques.
• Ability to manage multiple priorities, work under pressure, and communicate effectively across all levels.
• Degree in science, engineering, or manufacturing discipline desirable.
• Experience with ISO13485 and GMP compliance advantageous.

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