Preferred skills/knowledge in any of the following. Analytical Testing. Laboratory OOS. Validation Review/Approval. Change Control Review/Approval. Deviation Review/Approval. Purpose & Scope. Provide inter- and intradepartmental support in the preparation and review of documentation related to and including manufacturing processes, equipment, and computer systems that affect GMP-related activities. Review and approval of batch records. Essential ...
Purpose & Scope. This position will be responsible for the preventative maintenance, calibration, and repair of equipment in all areas of the facility. Essential Job Responsibilities. Position is responsible for various aspects of construction, start-up, validation support, and maintenance / calibration of all equipment, including electrical equipment and systems. Read schematics, scale controls, flow controls (air and liquid), and level controls...
. . Purpose & Scope. Perform daily activities related to the manufacture and packaging of pharmaceutical products while maintaining a safe, clean, and well-organized environment. Essential Job Responsibilities. Use master production records, specifications, and standard operating procedures to manufacture pharmaceutical products in accordance with cGMPs as defined in CFR, title 21. Perform basic maintenance and problem-solving on equipment within...
Purpose & Scope. Responsible for all areas relating to cost accounting reporting, fixed asset accounting, and assist in all other accounting activities including month-end close, new product pricing, financial reporting, year-end audit preparation, and budget and forecast activities. Essential Job Responsibilities. Ensure accurate and appropriate recording and analysis of revenues and expenses according to GAAP. Investigate variances and resolve ...
Preferred skills/knowledge in any of the following. Analytical Testing. Laboratory OOS. Validation Review/Approval. Change Control Review/Approval. Deviation Review/Approval. Purpose & Scope. Provide inter- and intradepartmental support in the preparation and review of documentation related to and including manufacturing processes, equipment, and computer systems that affect GMP-related activities. Review and approval of batch records. Essential ...
