Knowledge of cgmp expectations for laboratory records
This role is responsible for the development, qualification, and lifecycle management of compendial and internal reference standards supporting small-molecule programs
Job Summary
This role is responsible for the development, qualification, and lifecycle management of compendial and internal reference standards supporting small-molecule programs.
The position requires adherence to all Good Manufacturing Practices (GMP) and safety standards within a fully onsite laboratory setting in San Diego.
Thermo Fisher Scientific offers competitive remuneration ranging from $31.00 to $38.50 per hour along with comprehensive benefits including healthcare and retirement plans.
Matching Summary
This role is responsible for the development, qualification, and lifecycle management of compendial and internal reference standards supporting small-molecule programs.
Salary
Base: $31.00–$38.50 hourly; Bonus/Equity: Eligible for variable annual bonus; Benefits: Comprehensive package including medical, dental, vision, 401(k), and PTO
Skills & Requirements
Must-have
Bachelor's degree in Chemistry or Biochemistry
Proficiency in HPLC analysis and troubleshooting
Knowledge of cGMP expectations for laboratory records
Experience with analytical method validation activities
Ability to work onsite in San Diego, California
Nice-to-have
Strong project management skills in timeline-driven settings
Cross-functional collaboration experience with CMC teams
Proactive approach to process improvement ideas
Detail-oriented data evaluation capabilities
Key Requirements
Must be legally authorized to work in the United States without sponsorship
2+ years of relevant scientific experience or Master's degree
Pass a comprehensive background check including drug screening
Relocation costs are the responsibility of the candidate
Work Rights
Must be legally authorized to work in the US without sponsorship