2nd Shift: Aseptic Manufacturing Excellence Operator

Kindeva Drug Delivery; Bridgeton (MO); On-site; USD 52,000 - 72,000; Full time

Job summary

Kindeva Drug Delivery in Bridgeton, MO is seeking a Manufacturing Excellence Operator for first shift to support aseptic operations in a clean room. Responsibilities include equipment setup, sterilization prep, and adherence to cGMP standards.

The role emphasizes continuous improvement and cross-team collaboration in a highly regulated manufacturing environment. Candidates should have a high school diploma or GED with related experience, be proficient in reading instructions, and comfortable

Qualifications

• Must have high school diploma or GED with 2+ years related experience.
• Able to read and follow written instructions and SOPs.
• Capable of basic calculations and using measuring units.

Responsibilities

• Follow aseptic/sterile/cGMP techniques.
• Maintain cleanroom gowning and aseptic practices.
• Ensure cGMP compliance and report problems.
• Sanitize Clean Room areas per procedures.
• Maintain drug and raw material accountability.
• Log in-process test results per SOP/Batch Record.
• Unload sterilizers and verify counts for batches.
• Prepare solutions for other departments.
• Operate machines and hand-assemble components aseptically.
• Clear jams and perform tabletop adjustments.
• Set up/tear down/changeover Clean Room machinery.
• Complete training and stay current.
• Participate in continuous improvement events.
• Assist maintenance with equipment issues and asset care.
• Other duties as assigned.

Skills

GMP compliance

Aseptic technique

Equipment operation

Clean room gowning

Problem solving

Documentation

Safety procedures

Education

High school diploma or GED

Associate/Technical degree preferred

Tools

Computerized systems

Job description

Kindeva Drug Delivery in Bridgeton, MO is seeking a Manufacturing Excellence Operator for first shift to support aseptic operations in a clean room. Responsibilities include equipment setup, sterilization prep, and adherence to cGMP standards.

The role emphasizes continuous improvement and cross-team collaboration in a highly regulated manufacturing environment. Candidates should have a high school diploma or GED with related experience, be proficient in reading instructions, and comfortable