Slough - QA Specialist (GMP)

Location: Hybrid (Berkshire)

In this role, you will be responsible for maintaining and improving the quality assurance system to ensure that our products meet the required standards and comply with relevant regulatory requirements.

Key Responsibilities:

• Manage and investigate deviations, ensuring timely closure and documentation in accordance with GMP guidelines.
• Oversee the Corrective and Preventive Action (CAPA) system, including identification, investigation, root cause analysis, and implementation of corrective actions.
• Facilitate and document Change Control processes, ensuring all changes are properly evaluated, approved, and documented in compliance with regulatory requirements.
• Monitor and ensure adherence to GMP standards throughout production and manufacturing processes. Collaborate with cross-functional teams to support compliance initiatives and resolve quality-related issues.

Requirements:

• Bachelor’s degree in Life Sciences, Engineering, or a related field (or equivalent experience).
• At least 4 years of experience in a QA role within a GMP-regulated environment, with a strong understanding of industry standards.
• Extensive experience with deviations, CAPAs, and Change Control processes. Solid understanding of GMP regulations and their application in manufacturing settings.
• Strong analytical and problem-solving skills, with a focus on root cause analysis and continuous improvement.

Interested? Apply now for immediate consideration or contact Michael Owusu-Ansah on +44 203 928 6631 – mowusu-ansah@planet-pharma.co.uk

We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. Planet Pharma is an Employment Business providing Global Staffing services.