Manufacturing Specialist

Manufacturing Specialist- Didcot- Full-Time on Site (Shift Work)We’re seeking individuals who are eager to learn and have a foundational understanding of Good Manufacturing Practices (GMP). We are seeking rrelevant manufacturing experience in a production setting.You need to be happy with shift work.Shift ScheduleRotating shifts every two weeks:Day: 7 AM – 7 PMNight: 7 PM – 7 AMRole DurationInitial contract: 6 months- with possibility of extensionAbout the RoleThis is a unique opportunity to join a pioneering team focused on advancing mRNA technology and biopharmaceutical manufacturing. The organization is establishing a state-of-the-art research, development, and production facility at Harwell, dedicated to respiratory disease vaccine production. This initiative supports long-term public health goals and fosters collaboration with academic institutions, NHS, and government partners.As a Manufacturing Associate, you’ll operate advanced production equipment to support the safe and effective manufacture of mRNA-based vaccines. You’ll work in compliance with cGMP and health and safety regulations, ensuring batch quality and process integrity. The role blends scientific knowledge with operational and digital fluency, requiring strong attention to detail, adaptability, and teamwork.Key ResponsibilitiesOperate and monitor production equipment in compliance with cGMP, SOPs, and safety protocolsMaintain a clean and compliant work environmentExecute manufacturing operations and maintain accurate batch documentationPerform routine equipment maintenance (e.g., lubrication, filter changes)Troubleshoot equipment and digital systems efficientlyKeep training records and logs up to dateSupport manufacturing schedules with flexibility, including overtimeParticipate in deviation investigations, CAPA tasks, and incident analysisCollaborate with QA and cross-functional teams to meet production KPIsAdditional ResponsibilitiesPromote and practice safe work habitsIdentify and report safety or compliance concernsContribute to continuous improvement initiativesApply lean tools and digital platforms to enhance operationsThrive in a fast-paced, matrixed environment with a proactive mindsetKey Mindsets for SuccessDigital Fluency: Use digital tools to optimize production and ensure product integrityOwnership Mentality: Take initiative, solve problems, and improve workflows beyond your core responsibilitiesQualifications1+ years of experience in a GMP manufacturing environmentUniversity degree in pharmaceutical production technology or equivalentFull-time on-site availability requiredMay require enhanced pre-employment screeningPreferred SkillsExperience with filtration, chromatography, and cold chain managementFamiliarity with audit/inspection preparation and regulatory guidelinesStrong collaboration and communication skillsAbility to manage multiple tasks with minimal supervisionCommitment to values such as boldness, collaboration, curiosity, and perseverance

Created: 2025-08-13