Sr Operation Technician

at  Thermo Fisher Scientific

Singapore, Southeast, Singapore -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate05 Aug, 2024Not Specified06 May, 2024N/AGood communication skillsNoNo
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Description:

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work. And you’ll have the opportunity for continual growth and learning in a culture that empowers your development. With revenues of more than $40 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:

  • Lead activities done by the Clinical Trials Secondary Packaging Team
  • Perform all processes in accordance to established procedures and cGMP standards.
  • Maintain the facility and workspaces clean, neat and tidy.
  • Ensure that equipment and instruments in the work area is maintained and operating normally.
  • Complete regular reports (as required by Management or client) pertaining to relevant work area(s).
  • Maintain proper documentation for all processes conducted/performed.
  • Assist management in any other matters as required.
  • Responsible for managing all aspects of clinical trials supplies packaging, including supply forecast, batch record production, label production, and execution of the packaging exercise.
  • Planning and scheduling of labelling and/or packaging jobs.
  • Design and/or execute labelling and packaging instructions.
  • Ensure that Investigational Medicinal Products (IMPs) are labelled and packed in accordance with the requirements of each study protocol.
  • Identify, evaluate, select and manage third party contractors responsible for the production of labelling and packaging materials.
  • Generate and complete batch records.
  • Responsible for reconciliation of all packaging and labelling components.
  • Responsible for generation of batch records and production of specifications for all packaging and labelling components.
  • Produce Standard Operating Procedures and non-conformance reports.
  • Initiate and implement continuous improvement activities on productivity and quality.
  • Assist in Warehouse – receipt, retrieve, Problem Reporting (PR) and dispatch of Clinical Trial Materials – when necessary.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

Singapore, Singapore