Proficiency with hplc, uplc, uv-vis, and elisa instruments
This role involves executing routine in-process, drug substance, and stability test methods using various laboratory instrumentation
Job Summary
This role involves executing routine in-process, drug substance, and stability test methods using various laboratory instrumentation.
The successful candidate will maintain data integrity and ensure strict compliance with company SOPs and cGMP regulations.
Takeda offers competitive compensation including medical, dental, vision insurance, a 401(k) plan with match, and up to 80 hours of sick time annually.
Matching Summary
This role involves executing routine in-process, drug substance, and stability test methods using various laboratory instrumentation.
Salary
Hourly Wage Range: $24.76 - $38.87; Short-term incentives eligible for US based employees; Medical, dental, vision, 401(k) match, and paid vacation included
Skills & Requirements
Must-have
Bachelor's or master's degree in Life Sciences
0-3 years relevant laboratory experience
Proficiency with HPLC, UPLC, UV-Vis, and ELISA instruments
Knowledge of cGMP manufacturing regulations
Ability to work extended periods standing or sitting
Strong micropipetting and aseptic technique skills
Nice-to-have
Experience in a regulated pharmaceutical environment
Eagerness to learn and continuously improve
Good interpersonal and team collaboration skills
Willingness to work overtime or off-shift hours
Basic knowledge of chemical and biological safety procedures
Key Requirements
Bachelor's or master's degree in Life Sciences
0-3 years of relevant laboratory experience
Must be able to read, write, and converse in English
Basic computer skills including word processing and spreadsheets