Technical Operator (24/7 shift pattern)

Job description

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Fluctuating Temps hot/cold, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials, Working at heights Job Description Working shift pattern: 24/7 – 2 shifts on, 2 days off, 3 shifts on, 2 days off, 2 shifts on, 3 days off, etc.. Shifts will rotate between Day shift, 6.45am to 7pm, and Night shifts 6.45pm to 7am. We are currently hiring 3 Technical Operators to join our expanding team on 24/7 shifts —this is a fantastic opportunity to join a global leader with multiple openings available. With revenues of $20 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world. Responsibilities: Set up and operate bulking and/or aseptic filling lines in accordance with Standard Operating Procedures (SOPs) Complete all activities to acquire and maintain, as a minimum, a Bronze License Badge – Production areas (Grade C/D) access, including requalification every 2 years Manufacture pharmaceuticals following SOPs and Batch Manufacturing Records (BMRs) Perform Manufacturing, Filling, and Packaging operational duties, ensuring compliance with cGMP Set equipment to minimize downtime and product damage/waste, supporting start-ups, changeovers, and cleaning activities Monitor equipment status and report any faults or issues to supervision Clean and maintain clean rooms and equipment to regulatory standards Perform Clean In Place (CIP) and Steam In Place (SIP) activities Operate airlocks, autoclaves, and automated equipment cleaning systems Communicate instances of non-conformance for investigation and rectification Support project validation work and new product introduction Perform SAP transactions and use Quality systems for GMP changes and report writing Conduct basic equipment maintenance as needed Requirements: Experience in a pharmaceutical or regulated environment (MHRA and FDA regulations) Experience in cleanroom working, with knowledge of aseptic manufacturing and filling desirable Experience in spray drying systems, bulk GMP powder manufacturing, and powder filling Strong competency in English and Math, with a scientific background (e.g., A-Levels) essential Equivalent experience in a science-based subject is also acceptable Excellent communication and teamwork skills, with the ability to manage workload Experience in Lean systems and Continuous Improvement Understanding of HMI-driven pharmaceutical systems Aseptic block license will be considered a plus At Thermo Fisher Scientific, every single one of our 120,000 remarkable individuals has an unusual narrative to reveal. Join one of our new hires and become part of our outstanding mission—helping our customers make the world healthier, cleaner, and safer.