Job Type: Full Time
Shift: M-F, 8-4
Our client is a contract pharmaceutical manufacturer looking to add a quality chemist to their operation. An employee's responsibilities would include the analysis of raw materials, in-process materials, stability, and finished products in conformance with cGMP regulations in the lab, along with its daily operations.
- Responsible for the scheduling, calibration, and maintenance of equipment.
- Performs method development and validation for various analytical methods
- Work with raw materials to assess the quality of components for future products
- Use analytical lab equipment to measure and determine the validity of materials
Must have a bachelor's degree in either a science or engineering field
Must have cGMP knowledge/background within a lab and QMS experience
Must be able to run an HPLC, have dissolution (Disso) experience, and Compendial testing experience
Must have LIMS system experience and knowledge of ICH guidelines/stability
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