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Covingham, Swindon, United Kingdom, United Kingdom
Onsite
Work Schedule
OtherEnvironmental 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, No contact lens allowed; prescriptive glasses will be providedJob Description
Working shift pattern: 24/7 – rotating day and night shifts
When 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. With $20 billion in revenue and the industry's largest R&D investment, we give our people the resources and opportunities to make significant contributions to the world.
We are currently hiring 5 AVI & Packaging Operators to join our growing operations team. This is a great opportunity to secure one of five available positions in a high-performing pharmaceutical environment.
Responsibilities:
Set up and operation of the Automatic visual inspection & packing lines in accordance with Standard Operating Procedures (SOPs)
Perform AVI and packing of pharmaceutical products (Sterile & non-sterile) in accordance with Standard Operating Procedures (SOPs) and Batch Manufacturing Records (BMRs)
Perform AVI and Packaging operational duties, e.g., line clearance, In Process Checks (IPC) checks, replace components on line, complete batch & associated documentation, right first time in accordance with SOPs to ensure compliance with cGMP
Set equipment to ensure minimum downtime levels, minimum product damage/waste, support machine start-up, changeovers, testing and cleaning activities in accordance with SOP's and cGMP requirements
Monitoring equipment status and readiness for inspection & packing, reporting any faults or issues to Supervision
Cleaning and maintenance of clean rooms/equipment to SOPs, cGMP and pharmaceutical industry regulatory standards
To ensure any instances of non-conformance are communicated to the Process Coordinator, Area Manager, or Quality Assurance representatives to ensure that they are investigated and rectified
Support project validation work and new product introduction to the Operations department
SAP transactions
Using Quality systems for GMP changes and report writing.
Conduct and assist, where appropriate, in basic equipment maintenance
Tracking of progress and downtime reporting, escalating issues as appropriate.
Accurate and timely completion of the BMR, including online reviews, reconciliations, and MRP transactions, and complete Batch Notifications as required.
Maintenance of competency (suitably qualified and experienced) for the role through timely completion of training and, as appropriate, assessment and delivery of skills and knowledge training to others.
Contribute towards continuous improvement initiatives both through participation and putting forward ideas and suggestions.
Minimise material use and costs, without compromising quality, during batch running.
Cover operational requirements in the production area as required.
GMP:
Ensure products are inspected and packed, and documentation is completed in accordance with GMP and Standard Operating Procedures.
Support the Process Coordinator in performing Level 1 and Level 2 audits.
Support relevant Deviation and Complaint investigations and determination of appropriate CAPA as required.
Maintain a high level of tidiness and cleanliness at all times – personal, work area, and department.
Take ownership, accountability, and enforce good GMP and GDP within the GMP facility.
EH&S:
Understand emergency procedures and comply with safe systems of work.
Ensure compliance with environmental, health, and safety rules, signage, and instructions at all times.
Ensure prompt reporting and investigation of all accidents, near misses, and breaches of rules.
Qualifications/Experience:
Experience of working in a pharmaceutical or other regulated environment (MHRA and FDA regulations)
Experience of clean room working, knowledge of AVI, packaging, and serialization is highly desirable
Strong competency in English and Maths is essential, and a scientific background is essential (e.g. A-Levels)
Has supervised previously or has experience in developing individuals
Excellent communication and teamwork skills, with the ability to manage your own workload
Experience in Lean systems and Continuous Improvement (green belt would be desirable)
Understanding of HMI-driven pharmaceutical systems
At Thermo Fisher Scientific, each one of our 120,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner, and safer.