Join Tolmar as an Aseptic Manufacturing Operator I. This role focuses on producing high-quality injectable products in a cleanroom workplace while adhering to safety and GMP standards.
The Manufacturing
Operator I will contribute to the injectable team by assisting in the setup and operation of production equipment. This position requires attention to detail and the ability to work in a sterile setting.
Key responsibilities include sampling syringes, documenting activities, and training new operators on aseptic processes. Expect to engage in routine inspections that maintain quality standards and ensure product safety. Key Responsibilities:
Follow standard operating procedures to ensure quality
Assist in setup and operation of filling and packaging equipment
Perform biological sampling for clean room facilities
Document production activities accurately
Provide training for recent Aseptic Operators Requirements:
High school diploma or equivalent
1+ years experience in GMP manufacturing
Ability to stand for extended periods
Knowledge of cGMP standards
Effective verbal and written communication skills Become a vital part of Tolmar’s commitment to patient care and product integrity.