Job Title: QA Specialist (GMP)
Type: Contract
Location: Hybrid (Berkshire)
My client, a global pharmaceutical organisation currently seek a highly motivated and detail-oriented QA Specialist with strong experience in Deviation Management, Corrective and Preventive Actions (CAPAs), Change Control, and Good Manufacturing Practices (GMP). 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.
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.
Collaborate with cross-functional teams to support compliance initiatives and resolve quality-related issues.
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.
Strong analytical and problem-solving skills, with a focus on root cause analysis and continuous improvement.
Apply now for immediate consideration or contact Michael Owusu-Ansah on +44 203 928 6631 – mowusu-ansah@planet-pharma.We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.