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Packaging Engineer (Must Have Medical Device Packaging)

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Onsite

Packaging Engineer (Must Have Medical Device Packaging)

MillenniumSoft Inc

Packaging Engineer (Must Have Medical Device Packaging)

2 months ago

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Important information


Contract type:

Permanent

Location:

Vernon Hills, IL, USA

Work mode:

Onsite

Published on:

25 August 2026

What they need


Position: Packaging Engineer (Must Have Medical Device Packaging) Location: Vernon Hills, IL Duration: 8+ Months Contract **Total Hours/week: 40.00

pay rate: $30-40/hr** 1st Shift Client: Medical Device Company Job Category: Engineering Level Of Experience: Seniority Level Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only) No H1B’s Description Qualification Associate or Bachelor Degree equivalent in Packaging or in relatable field of study.

Experience 4 - 5 years of experience in medical Device packaging

Principal Accountabilities Demonstrates working knowledge of package engineering principles ; and techniques

  • Demonstrates working knowledge of legal requirements and documents.
  • Designs, prototypes and qualifies standard new packaging concepts in accordance with cGMP's with moderate guidance.
  • Evaluates and improves standard existing packaging concepts with moderate guidance.
  • Identifies, analyzes and specifies standard packaging materials and equipment with moderate guidance.
  • Supports external resource/contractors as required.
  • Has developed knowledge and skills in packaging; still acquiring / expanding fundamental knowledge and higher-level skills.
  • Applies knowledge and skills to a variety of standard activities.
  • Works with moderate guidance in own area of knowledge.

Special Skills

  • Effectively communicates technical knowledge and validates understanding of other packaging test methods/standards and related equipment.
  • Medical device packaging system development for flexible and rigid packaging applications.
  • Packaging system verification and validation experience
  • Experience with statistics and design of experiments.
  • Knowledge of the following standards: ISO 13485, ISO 11607,ISO 14971, EU MDR.

Accountability

  • Will not manage any direct reports.
  • Will not be responsible for any functional areas.
  • Knowledgeable and adherent to BD Quality and Corporate Policies.

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