Indianapolis 40K - 60K Permanent
Job Responsibilities:
Prepare and test raw materials, in-process samples, and finished products under supervision.
Perform routine analytical tests using techniques such as titration, pH measurement, dissolution, HPLC, or other laboratory methods as trained.
Record data accurately and maintain laboratory notebooks, worksheets, and electronic records according to cGMP standards.
Assist in sample collection, labeling, and inventory management.
Perform equipment cleaning, calibration checks, and basic maintenance under guidance.
Follow established SOPs and laboratory safety procedures, including proper use of PPE.
Support investigations of out-of-specification (OOS) results and assist with documentation.
Assist in QC projects, including stability studies, method verification, and validation support.
Collaborate with QC Chemists, QA personnel, and Manufacturing teams to support product release.
Qualifications:
Associate degree in Chemistry, Biochemistry, or related field; Bachelor’s preferred.
0–3 years of experience in a laboratory or manufacturing environment; pharmaceutical experience is a plus.
Familiarity with cGMP, SOPs, and laboratory safety practices.
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