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Packaging Engineer; Medical Device Packaging

Job in Franklin Lakes, Bergen County, New Jersey, 07417, USA
Listing for: MillenniumSoft Inc
Full Time position
Listed on 2026-06-13
Job specializations:
  • Engineering
    Packaging Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: Packaging Engineer (Must Have Medical Device Packaging)

Position

Packaging Engineer (Must Have Medical Device Packaging)

Location

Franklin Lakes, NJ

Duration

10+ Months Contract

Total Hours/week

40.00

Shift

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

Not applicable

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 with cGMPs 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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