Senior Medical Device Packaging Engineer: Process Validation

Katalyst CRO

Springfield (MO)

In loco

USD 70.000 - 100.000

Tempo pieno

14 giorni+

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Descrizione del lavoro

Katalyst CRO seeks a Packaging Engineer to support and improve packaging operations for medical device manufacturing. You will lead packaging process development, equipment qualification, and validation activities (IQ/OQ/PQ), ensuring robust, compliant packaging solutions.

Collaborating with Manufacturing, Quality, Regulatory, Operations, and Engineering, you will resolve issues, drive continuous improvement through Lean/Six Sigma, and maintain rigorous technical documentation.

Competenze

  • Bachelor's Degree in Packaging Engineering, Packaging Science, Mechanical Engineering, Chemical Engineering, or related Engineering discipline.
  • Engineering experience or equivalent advanced degree and relevant experience.
  • Experience in Medical Device, Healthcare, Pharmaceutical, or other regulated manufacturing environments preferred.
  • Knowledge of packaging validation, manufacturing processes, quality systems, and regulatory requirements.

Mansioni

  • Support and improve packaging operations for medical device manufacturing.
  • Lead packaging process development, equipment qualification, and validation activities (IQ/OQ/PQ).
  • Collaborate with Manufacturing, Quality, Regulatory, Operations, and Engineering teams to resolve production issues and drive continuous improvement.

Conoscenze

Lean Manufacturing
Six Sigma
Cross-functional collaboration
Problem solving
Project leadership
Technical communication
Regulatory compliance

Formazione

Bachelor's degree in packaging/engineering

Strumenti

IQ/OQ/PQ validation

Descrizione del lavoro

Katalyst CRO seeks a Packaging Engineer to support and improve packaging operations for medical device manufacturing. You will lead packaging process development, equipment qualification, and validation activities (IQ/OQ/PQ), ensuring robust, compliant packaging solutions.

Collaborating with Manufacturing, Quality, Regulatory, Operations, and Engineering, you will resolve issues, drive continuous improvement through Lean/Six Sigma, and maintain rigorous technical documentation.

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