Responsibilities:

Performs routine sample analysis, and a variety of tasks to support product development, ensuring agreed timelines
Assists method development
Performs method validation under supervision
Reports and resolved any unexpected issues under supervision
Complies with all relevant cGMP, and/or GLP regulatory requirements while carrying out assigned studies
Requirements:

B.S. in Chemistry, or related discipline with 3-5 years relevant experience in pharmaceutical, or related industry
M.S. or PhD in Chemistry
Hands-on experience with HPLC, UPLC, GC, LC/MS, IC, and Dissolution Testing
Excellent oral and written communication skills
Capable of setting priorities based on a fast-paced changing environment
Good team player to work with Formulators and QA
CRO experience is a plus


Associated topics: aseptic, bacteria, cytometry, immuno oncology, injury, medical, metabolism, nutritionist, pharmacy, toxicologist

* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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