Sr Operation Technician
at Thermo Fisher Scientific
Singapore, Southeast, Singapore -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 05 Aug, 2024 | Not Specified | 06 May, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
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