Job Details
Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good documentation procedures (GDPs), troubleshooting issues and review documentation as appropriate. Attain qualification for all assigned tasks and maintain individual training plans. Demonstrate proficiency at laboratory tasks, such as monitoring pH, conductivity, product sampling etc. May train Level 1 Associates on these tasks. Perform material movements, transfer materials and chemicals in, out, and across the production areas. Maintain facility and equipment through routine cleaning and sanitization, support 6S programs. Administrative tasks attending shift exchange, meetings, sending/receiving emails, participating in projects. Perform other duties as assigned. - Requirements:- High School Diploma or Equivalent minimum; AS/BS preferred; Preferred area of study: Science related discipline Prior work experience in a cleanroom, laboratory, other sterile setting is preferred. Prior experience with gowning or related PPE procedures in a sterile environment is preferred. Working experience in manufacturing; cGMP setting preferred, and/or some experience as an Associate Level I in bio-pharma industry. Able to follow documentation procedures for day to day tasks in a regulated industry Proven logic and decision making abilities, critical thinking skills. Strong written and verbal communication skills are required. The employee is living the cultural beliefs with the flexibility to adapt to changing business priorities. Is open to and actively seeks out feedback on their performance and translates that feedback into action. Employment Type: Full Time Bonus/Commission: Yes