U-09 Aseptic Production Support Operator

Kindeva Drug DeliveryBrentwood, MO
Onsite

About The Position

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

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.
  • Regularly required to use hands to finger, handle, or feel objects, tools, or controls.
  • Regularly required to stand and walk; climb or balance; and stoop, kneel, crouch, or crawl.
  • Must occasionally lift and/or move up to 40 pounds.
  • Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and the ability to adjust and focus.
  • Cannot be claustrophobic.
  • Position requires bending, stooping, squatting, pull/push and reaching above the shoulder level.

Responsibilities

  • Must be able to understand, follow, and operate applicable SOP’s and batch records for but not limited to, this equipment; i.e. Autoclaves, Gruenberg Oven, Crest Ultrasonic Cleaner, Huber washer, Capsolut, Drum Roller, and Bausch & Stroebel Washer.
  • Properly document all required entries on of 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 as well as perform and document line clearances.
  • Receive components, verify counts, and assign to batches.
  • Be knowledgeable cGMP’s as related to the above tasks.
  • Perform special projects as directed by the Supervisor.
  • Must be able to consistently follow all required environmental control procedures (example: glove changes, donning of designated coveralls and head covers, handling of components under laminar flow hoods, etc…
  • Must be able to perform cleaning of department including overhead work.
  • Other duties as assigned
  • Participate in process improvement activities.
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