This position reports directly to the QC Supervisor and is primarily responsible for performing analytical testing, laboratory investigations, and analytical method transfers for an OTC drug manufacturing facility. The role involves performing raw material, in-process, and release testing using a variety of analytical techniques while following cGMP, USP, and 21CFR 210/211 requirements.
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Job Type
Full-time
Career Level
Entry Level
Industry
Administrative and Support Services
Number of Employees
1,001-5,000 employees