Job Title: QA Specialist Industry: Biopharmaceuticals About the Role: Our client, a leading biotech company are seeking an experienced QA Specialist to join their growing Quality Assurance team. This is a fantastic opportunity to play a key role in maintaining high product quality standards in a regulated GMP environment while also supporting validation and qualification activities on-site. Key Responsibilities: Serve as a technical QA advisor on GMP, validation, and compliance topics Manage core QMS processes including deviations, CAPAs, change controls, audits, and complaints Review and approve batch records, SOPs, and validation protocols/reports Support qualification activities for facilities, equipment, and utilities during start-up and routine operations Apply quality risk management principles to ensure compliance and project timelines Collaborate with cross-functional teams including QC, Manufacturing, and Engineering Drive continuous improvement initiatives across QA processes Requirements: Bachelor's degree (or higher) in a scientific or engineering discipline Minimum 5 years' experience in QA within a GMP-regulated pharmaceutical or life sciences environment Hands-on experience with validation and a solid grasp of regulatory requirements Strong technical writing skills (SOPs, deviations, validation documentation) Excellent communication skills and ability to work independently and in cross-functional teams Fluent in English (written and spoken) Please note that this role can be offered on either a full-time or part-time basis, choose the hours that suit you! Onsite role- flexible work Skills: GMP Validation QA Benefits: Benefits