Job Description
Manufacturing Area Responsibilities: All aspects of sterile manufacturing including Aseptic Filling, Drug Substance Formulation and Preparation activities. Sterile Filling Product and component reconciliation. Set up and breakdown of single use materials. Materials handling, weighing, dispensing & formulation. Sample collection, processing, storage, and delivery. Equipment and parts cleaning using manual and automated methods and equipment. Area and Line equipment cleans & clearances. Operation and process monitoring of clean systems, autoclaves, and processing equipment. Preferred Qualifications: 3+ plus years of experience in a GMP/ other regulated environment. Demonstrated knowledge of GMP principles. Ability to perform assignments with a high degree of focus/attention to detail. Ability to maintain focus during repetitive tasks over the course of a shift. Drug Product manufacturing experience an advantage. Ability to assemble, disassemble, operate, and understand simple to moderately complex equipment per procedures. Ability to work effectively in an individual and within a team environment. Ability to accurately document process tasks in batch manufacturing records. Coachable, ability to take coaching/critique and show learned/measurable improvement. Capacity to follow written procedures, recognize and report malfunctions. Strong communication skills. Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative. BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES. Skills: Manufacturing Sterile Pharmaceuticals