Associate Production Scientist
Verona, Wisconsin, United States
Efficient and safe manufacturing of advanced pharmaceutical ingredients (APIs), maintaining current Good Manufacturing Practices (cGMP) requirements in kilo labs (500g to 3 Kg), pilot, and production plants (15 to 100 Kg). Responsibilities and participation on this rule include the following:• Laboratory practice implementation per FDA, OSHA, EPA, DNR, DOT, and other regulatory agencies while maintaining accurate records, and being in control of preventive equipment maintenance and safety audits as needed. • Project lead: Manufacturing representative responsible for facilitating coordination, communication, and written reports between Quality, Project Management, Inventory, and external customers on a professional level during the execution of the GMP run. • Shift lead: Accountable for standing in for the 3rd shift supervisor when absent, to overcome production obstacles as they arise for a period of time.• Effectively completed tasks in a project-specific team environment enhancing productivity by cutting production times.• Be proficient with operational software: SAP ERP, MANGO, and TrackWise.