Technical Operator - Double Days
View: 107
Update day: 07-05-2024
Location: Swindon South West
Category: Production / Operation Maintenance Science Labor Pharmaceutical / Chemical / Biotech
Industry:
Job content
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 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 operation of aseptic filling lines in accordance to Standard Operating Procedures (SOPs).
- Preparation, testing and set of multiple modules in readiness for manufacturing and fill/finish processes –
- CIPs. SIPs, Filter Integrity testing, Pressure Tests, Autoclaving, Decontamination by VHP and cleanroom cleaning.
- Set up, operation of small, large scale compounding systems in accordance to Standard Operating Procedures (SOPs).
- Formulation of Pharmaceuticals utilizing bespoke manufacturing skids, vessel systems in compliance to batch manufacturing records.
- Perform Manufacturing, Filling, operational duties, e.g. line clearance, In Process Checks (IPC) checks, replace components on line, complete batch & associated documentation, right first time for 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 production, reporting any faults or issues to Supervision
- Cleaning and maintenance of clean rooms/equipment to SOPs, cGMP and pharmaceutical industry regulatory standards.
- Perform Clean In Place (CIP) and Steam In Place (SIP) activities using HMI controlled systems.
- Operation of airlocks, autoclaves, automated vessels/ equipment cleaning systems to ensure that all equipment is sterilised ready for use.
- To ensure any instances of non-conformance are communicated to the area leader, Manager or Quality Assurance representatives to ensure that they are investigated and rectified.
- Support project validation work, 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.
- Conduct clean room environmental monitoring in accordance to in house procedures.
- Maths GCSE (Grade C or Above)
- English GCSE (Grade C or above)
- Experience of working in a regulated industry e.g. Pharmaceuticals
- Previous experience of working in a manufacturing environment – desirable
- Basic IT user including MS Office
Deadline: 21-06-2024
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