AVI/Labelling Technical Operator
at Thermo Fisher Scientific
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Work ScheduleOtherEnvironmental ConditionsAble to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, No contact lens allowed; prescriptive glasses will be provided, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)Job DescriptionJob DescriptionWorking shift pattern: 24/7 – rotating day and night shiftsWhen you’re part of Thermo Fisher Scientific, you’ll do challenging work and be part of a team that values performance, quality, and innovation. As part of a successful, growing global organization, you will be encouraged to perform at your best.We are currently hiring 6 AVI & Packaging Operators to join our growing operations team. This is a great opportunity to secure one of six available positions in a high-performing pharmaceutical environment.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 Automatic Visual Inspection (AVI) and packing lines in accordance with Standard Operating Procedures (SOPs)Perform AVI and packing of pharmaceutical products (sterile and non-sterile) in line with SOPs and Batch Manufacturing Records (BMRs)Carry out AVI and packaging operational duties including line clearance, in-process checks (IPCs), component replacement, and batch documentation—ensuring right-first-time compliance with cGMPSet and adjust equipment to minimize downtime, reduce product waste, and support start-ups, changeovers, testing, and cleaning activitiesMonitor equipment status and readiness for inspection and packing, reporting faults or issues to supervisionClean and maintain cleanrooms and equipment in line with SOPs, cGMP, and regulatory standardsCommunicate any non-conformance issues to the Process Coordinator, Area Manager, or Quality Assurance for investigation and resolutionSupport validation activities and new product introductions within the Operations departmentUse quality systems for GMP changes and report writingConduct and support basic equipment maintenance activitiesGMP Responsibilities:Ensure products are inspected, packed, and documented in full compliance with GMP and SOPsSupport the Process Coordinator with Level 1 auditsAssist with deviation and complaint investigations, including CAPA implementationMaintain high standards of cleanliness and organisation (personal, work area, and department)Take ownership and accountability for maintaining strong GMP and GDP standards across the facilityEH&S Responsibilities:Understand emergency procedures and follow safe systems of workComply with all environmental, health, and safety policies, signage, and instructionsPromptly report and support investigation of accidents, near misses, and safety breachesQualifications & Experience:Experience in cleanroom environments; knowledge of AVI, packaging, and serialization is highly desirableStrong competency in English and Maths; scientific background (e.g., A-Levels) preferredExcellent communication and teamwork skills, with the ability to manage workload effectivelyUnderstanding of HMI-driven pharmaceutical systemsAt Thermo Fisher Scientific, each one of our 120,000 extraordinary minds has a unique story to tell. Apply now to be one of our 6 new hires and contribute to our mission—enabling our customers to make the world healthier, cleaner, and safer.
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