Temp Associate Technician, THV Sewing (2nd Shift)

JENAVALVE TECHNOLOGY INCIrvine, CA
$24 - $24Onsite

About The Position

Manufacturing entry-level technician responsible for performing detailed sewing and tissue preparation processes used in the assembly of transcatheter heart valve devices. This role requires high manual dexterity, attention to detail, and adherence to strict regulatory, quality, and contamination control procedures within a controlled cleanroom manufacturing environment.

Requirements

  • High school diploma or equivalent required. Candidates without a diploma may demonstrate equivalent competency through a validated external assessment designed to evaluate comprehension, language, and related abilities at a high school level.
  • Ability to use small hand tools, steady hand-eye coordination, and high manual dexterity/fine motor skills.
  • Must have ability to perform detailed tasks accurately.
  • Must be able to handle animal tissue and wet processes.
  • Must be able to work effectively and collaborate within cross functional teams.
  • Ability to read, comprehend and speak English, and good communication skills required.
  • Knowledge of and adherence to Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing.
  • Successful completion of required training and demonstrated competency on assigned manufacturing processes.
  • Adhere to all rules and requirements and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control.
  • Basic computer skills.

Responsibilities

  • Use tools – needles, scissors, forceps, specialized tooling, microscope – to perform assigned steps, in rotation, in the sewing assembly of valves.
  • Perform verifications, against specifications, of completed steps, and execute work in assembly line.
  • Review, follow, and perform job functions in compliance with established work instructions and adherence with SOPs, including recording traceable information on device history records.
  • Support activities correspond to other work procedures, as requested, to provide support to operations processes.
  • Assist Engineering in root cause analysis investigation for component nonconformance.
  • Maintain compliance with company Quality Management System requirements, including applicable Good Manufacturing Practices (GMP) and regulatory standards.
  • Maintain reliable and consistent attendance to support production operations, including punctual arrival and the ability to work full scheduled shifts and overtime as required to meet operational and production needs.
  • General work area housekeeping.
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