Aseptic Manufacturing Excellence Operator (2nd Shift)

VetJobs; St. Louis (MO); On-site; USD 60,000 - 75,000; Full time

Job summary

Kindeva is hiring a Manufacturing Excellence Operator for the St. Louis, MO area.

This second-shift role supports aseptic operations in a clean room, including setup, disassembly, and operation of high-speed equipment, and preparation of sterilized components in accordance with cGMP. Responsibilities include maintaining gowning standards, documenting results, unloading sterilizers, preparing solutions, and performing routine equipment changeovers while adhering to SOPs.

Qualifications

• Must follow aseptic/sterile/cGMP techniques.
• Ability to read and comprehend technical documents.
• Proficiency with basic calculations and measurements.

Responsibilities

• Follow aseptic/sterile/cGMP techniques at all times.
• Maintain cleanroom gowning and aseptic principles.
• Ensure compliance with cGMP and SOPs; report issues to supervisor.
• Sanitize Clean Room areas per procedures and maintain accountability of materials.
• Record in-process test results and logbooks with accuracy.
• Unload sterilizers, handle components, verify counts, assign batches.
• Prepare solutions for other departments; perform housekeeping duties.
• Operate assigned machines and aseptically hand assemble components.
• Clear jams and perform tabletop adjustments on equipment.
• Set up, tear down and changeover Clean Room machinery.
• Complete training requirements on target times and stay current.
• Participate in continuous improvement activities.
• Assist maintenance with equipment issues; perform asset care.

Skills

Aseptic technique

Cleanroom procedures

Documentation quality

Education

High school diploma or GED

Associates or Technical Degree preferred

Job description

Kindeva is hiring a Manufacturing Excellence Operator for the St. Louis, MO area.

This second-shift role supports aseptic operations in a clean room, including setup, disassembly, and operation of high-speed equipment, and preparation of sterilized components in accordance with cGMP. Responsibilities include maintaining gowning standards, documenting results, unloading sterilizers, preparing solutions, and performing routine equipment changeovers while adhering to SOPs.