Loading ...

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.
Minimum Requirements/Qualifications:
  • 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
At Thermo Fisher Scientific, each one of our 70,000 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.
Loading ...
Loading ...

Deadline: 21-06-2024

Click to apply for free candidate

Apply

Loading ...
Loading ...

SIMILAR JOBS

Loading ...
Loading ...