UPM pharmaceuticals
On-site
Not Disclosed
Pharma
R&D
Chemist I, II, III, or Senior is responsible for performing pharmaceutical laboratory and quality-control testing of raw materials, in-process materials, finished products, residuals, and stability samples. The role includes operating and maintaining laboratory equipment, analytical testing, documentation, method transfers, validation studies, and compliance with cGMP, SOPs, USP/NF, and other applicable regulations. The required experience ranges from 2+ years for Chemist I to 10+ years for Senior Chemist.
The Pharmaceutical Chemist performs set up, calibration, operation, and maintenance of laboratory test equipment. Performs assigned work in a timely and safe manner conforming to regulatory, company, and compendial requirements. Adheres to cGMP, which include, but is not limited to, proper laboratory documentation and maintenance, and archiving of paperwork. Compiles reports of analytical tests, ensuring reports are accurate and complete with documentation of procedures, equipment, and reagents used in analytical testing. Develops proficient practical laboratory skills, a thorough knowledge of chemistry theories, analytical techniques, and adopts site procedures as required. Assists in the execution of protocols, method transfers, and validation studies under the guidance of more experienced analysts. May need training in the handling of controlled substances. The Pharmaceutical Chemist performs routine and non-routine quality control testing of raw materials, in process, residual, finished product, and stability testing within the framework of the site policies and cGMP regulations. Participates in special studies to accomplish company and departmental goals. Records and reports data accurately and incompliance with current methods/SOPs, USP/NF, other compendia as applicable, and cGMP. Performs duties under the guidance of laboratory management or designee.
Degree
BachelorSpecialization
Chemistry2-12 yrs
Job ID:
CGXP_26_21546