Perform and document daily manufacturing operations in a cGMP environment. This involves operation of process equipment, execution of validation protocols, creating/ revising cGMP documents and other assignments. Applicants will be highly detailed oriented with excellent documentation skills. Applicants will become trained and skilled at most or all unit operations in their area, often leading the execution of procedures, and performs most functions with minimal supervision. Due to continued growth and the introduction of new technologies across the site, we are looking to identify candidates at all experience levels. You will have an opportunity to experience various areas of our manufacturing process while making an immediate impact within multiple departments. Applicants will be detail oriented, interested in learning and developing in a cGMP environment.
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Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
Number of Employees
1,001-5,000 employees