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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 Schedule Rotating shifts every two weeks: • Day: 7 AM – 7 PM, • Night: 7 PM – 7 AM Role Duration • Initial contract: 6 months- with possibility of extension About the Role This 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 Responsibilities • Operate and monitor production equipment in compliance with cGMP, SOPs, and safety protocols, • Maintain a clean and compliant work environment, • Execute manufacturing operations and maintain accurate batch documentation, • Perform routine equipment maintenance (e.g., lubrication, filter changes), • Troubleshoot equipment and digital systems efficiently, • Keep training records and logs up to date, • Support manufacturing schedules with flexibility, including overtime, • Participate in deviation investigations, CAPA tasks, and incident analysis, • Collaborate with QA and cross-functional teams to meet production KPIs Additional Responsibilities • Promote and practice safe work habits, • Identify and report safety or compliance concerns, • Contribute to continuous improvement initiatives, • Apply lean tools and digital platforms to enhance operations, • Digital Fluency: Use digital tools to optimize production and ensure product integrity, • Ownership Mentality: Take initiative, solve problems, and improve workflows beyond your core responsibilities Qualifications • 1+ years of experience in a GMP manufacturing environment, • University degree in pharmaceutical production technology or equivalent, • Full-time on-site availability required, • May require enhanced pre-employment screening Preferred Skills • Experience with filtration, chromatography, and cold chain management, • Familiarity with audit/inspection preparation and regulatory guidelines, • Strong collaboration and communication skills, • Ability to manage multiple tasks with minimal supervision, • Commitment to values such as boldness, collaboration, curiosity, and perseverance