Join Tolmar as an Aseptic Manufacturing Operator I. This role focuses on producing high-quality injectable products in a cleanroom environment 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 environment. Key responsibilities include sampling syringes, documenting activities, and training current 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 new 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.
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