Responsible for monitoring production areas to ensure quality and compliance with all SOPs, cGMP, company policies as well as FDA and other government and safety regulations by performing the following duties. Major Job Duties: Perform record reviews, inspections, and physical testing. Identify, investigate, and prepare reports on quality issues. Interpret generated data and communicate results to Quality management. Maintain effective communication and partnership with Operations department. Adapt to changes in the work environment and must be able to change shifts as needed.
3 shift (M-F: 8 hrs/shift) operation/rotation
* 2 Shift (Fri-Sun: 12 hrs/shift) operation/rotation
Education: High school diploma at minimum with 4 years cGMP experience; prefer 2 year technical or scientific degree with 2 years of experience, or 4 year degree with no experience.