Our client, a global joint preservation company, has an immediate opening for a Manufacturing Technician. This role will be responsible for the formulation, filling, and packaging of medical device products while adhering to cGMP guidelines, regulatory standards, and company-specific protocols.

Responsibilities:

• Operate production equipment, ensuring high levels of safety and quality in the manufacturing of medical devices
• Execute dissolution, reaction, filtration, formulation, and filling activities for aseptic and terminally sterilized products
• Follow established procedures for clean out of place (COP), clean in place (CIP), steam in place (SIP), and autoclaving of equipment and components
• Perform room sanitization and other activities to maintain controlled environment conditions
• Strictly adhere to written work instructions and standard operating procedures (SOPs)
• Document and verify all manufacturing and quality data on controlled forms and batch records
• Report any deviations or nonconformance to management promptly
• Maintain current training on all relevant procedures, including reading and understanding SOPs, as well as completing required skills development and classroom training
• Ensure compliance with cGMP, regulatory standards, and internal procedures during all work activities
• Contribute to team projects that support company growth and operational improvements

Requirements:

• Minimum 6 months of experience working in a cleanroom environment
• AS degree with 2+ years of experience or a High School diploma with 4+ years of experience in cGMP manufacturing
• 4+ years of experience in a regulated manufacturing environment
• Hands-on experience working in a cleanroom and applying aseptic techniques
• Familiarity with operating automated commercial-scale equipment
• Ability to work effectively in a results-driven, team-oriented environment