Scientist I, Formulations
at Thermo Fisher Scientific
Fremont, CA 94555, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 14 Nov, 2024 | USD 86000 Annual | 17 Aug, 2024 | 1 year(s) or above | Regulations,Chemical Handling,Pipetting,Iso,Chemistry,Hazardous Chemicals,Laboratory Skills,Biochemistry,Gmp | 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:
EDUCATION
- High shool diploma or equivalent required
- BS/BA in scientific field (Chemistry or Biochemistry preferred)
- Equivalent combination of education and years of related experience may be substituted
EXPERIENCE
- 1+ years of related experience and/or training preferred
- IVD immunoassay manufacturing experience is preferred
- Experience in working with potentially hazardous chemicals and human source materials preferred
- Familiarity with Quality System Regulations and ISO 13485 regulations is a plus
KNOWLEDGE, SKILLS, ABILITIES
- Strong laboratory skills including pipetting, safety, and hazardous chemical handling and knowledge of safety precautions
- Ability to perform tasks in compliance with GMP, GDP, QSRs, ISO and IVD regulations
- Ability to be organized and detail oriented to be able to prioritize own and other’s work and meet business productivity metrics
- Self-sufficient, self-motivated, and focused
PHYSICAL REQUIREMENTS / WORK ENVIRONMENT
- Ability to routinely lift 25 pounds
Responsibilities:
- Manufacture products including reagents, calibrators, buffers, controls, and intermediates, and complete batch records while maintaining cGMPs and GDP standards
- Perform in-process testing using clinical analyzers, review and analyze data
- Review other manufacturing operators/scientist’s batch records
- Maintain and analyzes lot histories for trends and discrepancies
- Perform laboratory activities including weighing, transferring, and mixing required chemicals and performing product filtration
- Participate in process improvement projects to improve efficiencies and support business needs
- May modify SOPs, work instructions and reports with guidance
- Initiate and support investigations for nonconformances and deviations
- Maintain and troubleshoot equipment as appropriate
- Keep department supervisor and/or manager updated on all issues
- Perform other job duties as required
REQUIREMENT SUMMARY
Min:1.0Max:6.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Diploma
Proficient
1
Fremont, CA 94555, USA