Packaging Engineer II — Medical Device Validation

Grove Technical Resources, Inc.

North Haven (CT)

On-site

USD 41,000 - 63,000

Full time

23 hours ago
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Job summary

Grove Technical Resources, Inc. is seeking a Packaging Engineer II to support packaging material qualification and process validation for medical device products, specifically absorbable sutures.

This fixed-term contract involves hands-on qualification of materials and equipment, protocol development, and cross-functional collaboration. Ideal candidates bring IQ/OQ/PQ experience, familiarity with vision inspection systems, and strong documentation skills to ensure compliance with medical device

Qualifications

  • Hands-on IQ, OQ, PQ experience with process validation.
  • Knowledge of Cognex and Keyence vision inspection systems is preferred.
  • DOE and Minitab knowledge is preferred.
  • Medical device industry experience is a plus.
  • Strong communication and documentation skills are essential.

Responsibilities

  • Validate and qualify packaging materials such as nylon film, foil, and Tyvek.
  • Perform equipment qualification (IQ, OQ, PQ) and process validation.
  • Develop validation protocols, reports, and SOPs.
  • Support process development and change control activities.
  • Lead projects and coordinate with cross-functional teams.
  • Ensure compliance with medical device quality standards.

Skills

IQ/OQ/PQ experience
Process validation
Strong communication
Documentation skills

Tools

Cognex vision systems
Keyence vision systems
Design of Experiments (DOE)
Minitab

Job description

Grove Technical Resources, Inc. is seeking a Packaging Engineer II to support packaging material qualification and process validation for medical device products, specifically absorbable sutures.

This fixed-term contract involves hands-on qualification of materials and equipment, protocol development, and cross-functional collaboration. Ideal candidates bring IQ/OQ/PQ experience, familiarity with vision inspection systems, and strong documentation skills to ensure compliance with medical device

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