Aseptic Manufacturing Excellence Operator (2nd Shift)

Kindeva

Bridgeton (MO)

Hybrid

USD 38,000 - 52,000

Full time

14 days+

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Job summary

Kindeva in St. Louis, MO is seeking a Manufacturing Excellence Operator for second shift in a clean room environment. The role supports aseptic operations, setting up, disassembling and operating high-speed equipment, and sterilizing components.

You will follow cGMP standards, maintain documentation, and participate in continuous improvement while ensuring batch records and material accountability. Strong attention to detail and ability to read SOPs are essential.

Qualifications

  • High school diploma or GED with 2+ years related experience; associates preferred.
  • Ability to read instructions and present information effectively.
  • Numerical calculations for accountability and density.
  • Proficient with computerized systems and software.
  • Ability to follow detailed documentation and SOPs.

Responsibilities

  • Follow aseptic/sterile/cGMP techniques at all times.
  • Maintain gowning and aseptic technique inside the processing area.
  • Ensure cleanroom processes comply with cGMP; report problems.
  • Sanitize Clean Room areas per procedures.
  • Handle drug materials accountability and batch records.
  • Unload and assemble components; prepare solutions; perform housekeeping.
  • Operate and troubleshoot assigned machines; assist in preventive maintenance.
  • Complete training targets on schedule; participate in continuous improvement.

Skills

Aseptic Operations
Gowning & Cleanroom Protocols
Equipment Operation
Documentation & GMP
Reading Technical Instructions

Education

High school diploma or GED
Associates or Technical Degree preferred

Job description

Kindeva in St. Louis, MO is seeking a Manufacturing Excellence Operator for second shift in a clean room environment. The role supports aseptic operations, setting up, disassembling and operating high-speed equipment, and sterilizing components.

You will follow cGMP standards, maintain documentation, and participate in continuous improvement while ensuring batch records and material accountability. Strong attention to detail and ability to read SOPs are essential.

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