U-09 Aseptic Production Support Operator

KindevaBrentwood, MO
Onsite

About The Position

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. This role is responsible for understanding and operating applicable SOPs and batch records for various equipment, documenting all required entries, performing and documenting verifications, cleaning equipment, performing line clearances, receiving and assigning components, and adhering to cGMPs. The position also involves performing special projects, following environmental control procedures, cleaning the department (including overhead work), and participating in process improvement activities.

Requirements

  • High school diploma / general education degree (GED) or an Associate’s degree plus 1 year Manufacturing / Packaging work experience or Veterans/Military.
  • Ability to read and comprehend simple instructions, correspondence, and memos.
  • Ability to write correspondence.
  • Ability to effectively present information in one-on-one and small group situations to other employees of the organization.
  • Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.
  • Ability to apply commonsense understanding to carry out instructions furnished in written, oral or diagram form.
  • All new external applicants will be required to pass an assessment test.
  • Cannot be claustrophobic.

Responsibilities

  • Understand, follow, and operate applicable SOP’s and batch records for equipment such as Autoclaves, Gruenberg Oven, Crest Ultrasonic Cleaner, Huber washer, Capsolut, Drum Roller, and Bausch & Stroebel Washer.
  • Properly document all required entries on batch records, logbooks, and sterilization records, including proper performance and documentation of in-process checks.
  • Properly perform and document verification of other technicians on batch records and sterilization records.
  • Properly clean equipment and perform and document line clearances.
  • Receive components, verify counts, and assign to batches.
  • Be knowledgeable of cGMP’s as related to the tasks.
  • Perform special projects as directed by the Supervisor.
  • Consistently follow all required environmental control procedures (e.g., glove changes, donning of designated coveralls and head covers, handling of components under laminar flow hoods).
  • Perform cleaning of the department, including overhead work.
  • Participate in process improvement activities.
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service