What are the responsibilities and job description for the Manufacturing Operator I - Portsmouth, NH position at Unicon Pharma Inc?
Job Description
Job Description
Description :
- The Manufacturing Services Associate I is responsible for supporting all cGMP manufacturing production suites.
- They support the production groups by ensuring the suites are appropriately stocked with raw materials and consumables, assemble and autoclave assemblies for use, clean soiled parts, perform daily / weekly maintenance on analytical equipment, and complete scheduled cleaning requirements that are not fulfilled by Client's contracted cleaning staff.
- They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique and cross contamination awareness in handling of products and materials.
- Perform 6S and stock each suite daily, clean soiled parts daily.
- Determine production needs for autoclaved assembles and deliver to suites.
- Perform daily and weekly maintenance activities on analytical equipment.
- Perform weekly and monthly cleans of inoculum rooms.
- Report all activities in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate.
- Attain qualification for all assigned tasks and maintain individual training plan
- Prepare materials for transport and delivery to manufacturing suites. Perform material movements into, out of, and across the production areas.
- Maintain facility and equipment through routine cleaning and sanitization.
- Administrative tasks attending suite shift exchange, meetings, sending / receiving emails, participating in projects, perform other duties as assigned.
- Perform other duties as assigned.
