What are the responsibilities and job description for the Production/manufacturing planner position at Tekgroup?
- The Manufacturing Associate is responsible for producing therapeutic proteins (API) in compliance with cGMP (current Good Manufacturing Practices) guidelines. Associates will follow established process recipes, adhere to written Standard Operating Procedures (SOPs), monitor equipment and processes, and carry out basic laboratory tasks such as pH testing, conductivity measurement, sampling, and routine sanitization of facilities and equipment.
- Associates will receive close supervision while developing a foundational understanding of cGMP compliance and demonstrating proper aseptic techniques when handling products and materials. Responsibilities include setting up, operating equipment, and overseeing production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations. Associates will also document production activities in both written and electronic formats, following GMP and GDP guidelines, and review documentation when necessary.
- Associates are expected to complete training for all assigned tasks and maintain an individual training plan. Material handling responsibilities include transferring raw materials and chemicals within production areas. Routine cleaning and sanitization of the facility and equipment are essential, and associates will also support the 6S (workplace organization) program.
- The role requires working in a cleanroom environment, including gowning as necessary. Administrative duties include attending shift handovers, meetings, sending/receiving emails, and participating in projects as assigned. Additional tasks may be assigned as needed.
Job Types: Full-time, Contract
Pay: $20.00 - $23.00 per hour
Experience:
- Manufacturing: 5 years (Preferred)
- QAD systems: 5 years (Preferred)
Work Location: In person
Salary : $20 - $23
