Planet Pharma
Job Description
Alternate Saturdays, Sunday - Tuesday 1800 - 0700. This role primarily involves night and weekend shift hours, with occasions where flexibility is required as shift hours can vary depending on operational demands. Responsibilities
Provide on-the-floor QA oversight and support to manufacturing operations Review executed batch records and associated documents to ensure compliance with approved procedures and cGMP expectations Respond to quality-related incidents or non-conformances on the floor and secure necessary documentation for real-time investigations Represent QA in support of deviations including active participation in Root Cause Analysis (RCA) Provide cGMP and compliance guidance to Manufacturing and Novato Technical Services (NTS) personnel Provide QA support including authoring, review, and approval of documents in Quality Management Systems in accordance with company policies Perform area walkthroughs Perform other duties and projects as assigned by management Requirements
B.S. in scientific discipline or equivalent work experience. Prior batch record execution or review experience. Prior experience in investigation, change control, other Quality Management Systems (QMS) Working knowledge of cGMPs Excellent written and verbal communication and interpersonal skills Must display strong analytical and problem-solving skills Manufacturing and Manufacturing Sciences experience preferred The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
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Alternate Saturdays, Sunday - Tuesday 1800 - 0700. This role primarily involves night and weekend shift hours, with occasions where flexibility is required as shift hours can vary depending on operational demands. Responsibilities
Provide on-the-floor QA oversight and support to manufacturing operations Review executed batch records and associated documents to ensure compliance with approved procedures and cGMP expectations Respond to quality-related incidents or non-conformances on the floor and secure necessary documentation for real-time investigations Represent QA in support of deviations including active participation in Root Cause Analysis (RCA) Provide cGMP and compliance guidance to Manufacturing and Novato Technical Services (NTS) personnel Provide QA support including authoring, review, and approval of documents in Quality Management Systems in accordance with company policies Perform area walkthroughs Perform other duties and projects as assigned by management Requirements
B.S. in scientific discipline or equivalent work experience. Prior batch record execution or review experience. Prior experience in investigation, change control, other Quality Management Systems (QMS) Working knowledge of cGMPs Excellent written and verbal communication and interpersonal skills Must display strong analytical and problem-solving skills Manufacturing and Manufacturing Sciences experience preferred The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
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