Microbiologist I
at Thermo Fisher Scientific
Singapore, Southeast, Singapore -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 24 Sep, 2024 | Not Specified | 24 Jun, 2024 | 2 year(s) or above | Environmental Monitoring,Excel,Powerpoint,Regulatory Requirements,Time Management,Microbiology,Project Management Skills,Biology,Biologics | 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:
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or growing efficiency in their laboratories, we are here to support them. Our distributed team of more than 75,000 colleagues delivers an outstanding combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. For more information, please visit www.thermofisher.com.
Responsibilities:
- To perform quality control microbiological testing of raw materials, incoming goods, intermediates, and/or finished products under cGMP conditions for QC release or as part of stability studies
- To support monitoring for facility’s utilities systems
- To support equipment qualification
- To perform and coordinate calibration, and maintenance of laboratory equipment
- To be involved in aseptic process simulations
- To support method transfer/verification/validation for new product introduction
- To perform periodic reviews for laboratory documents
- To lead microbiological inventory management
- To maintain the accuracy, completeness, and compliance of laboratory data
- To maintain individual’s training records
- To support continuous improvement activities
- To communicate in site and global platforms
- To ensure cGMP is applied and adhered to in their area of work
- To collaborate with HSE, cGMP and always maintain a 5S approach
- To perform tasks required by the Manager
- To support shift work (when required
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Biology
Proficient
1
Singapore, Singapore