This fully onsite role involves conducting scientific method development, validation projects, and troubleshooting for pharmaceutical compounds in a GMP laboratory
Job Summary
This fully onsite role involves conducting scientific method development, validation projects, and troubleshooting for pharmaceutical compounds in a GMP laboratory.
The successful candidate will independently design experiments, lead analytical troubleshooting sessions, and write comprehensive study protocols and reports.
Thermo Fisher Scientific offers a global team environment that values passion, innovation, and commitment to scientific excellence with opportunities for professional development.
Matching Summary
This fully onsite role involves conducting scientific method development, validation projects, and troubleshooting for pharmaceutical compounds in a GMP laboratory.
Skills & Requirements
Must-have
HPLC GC UPLC LC-MS instrument operation
Method development and validation expertise
GMP GLP compliance knowledge
Root cause analysis and troubleshooting
Technical writing and protocol creation
Stability and inhalation testing procedures
Nice-to-have
Experience with extractable leachable studies
Ability to mentor junior staff members
Presentation skills for technical conferences
Collaborative team work environment
Business development support experience
Key Requirements
Bachelor's degree or equivalent qualification
8+ years of relevant industry experience
Must be legally authorized to work in the US without sponsorship
Pass comprehensive background check including drug screening
Work Rights
Must be legally authorized to work in the United States