Senior Packaging Engineer (BioSurgery Division | Project Shield)

Senior Packaging Engineer (BioSurgery Division | Project Shield)

Contract Type:

Contract

Location:

Raritan - NJ

Industry:

Information Technology

Contact Name:

Jill Jones

Contact Email:

jilljones@dewintergroup.com

Contact Phone:

(510) 949-5960

Date Published:

11-05-2025

Salary:

$40.00 - $55.00 Per Hour

Job ID:

37859

Title:  Senior Packaging Engineer (BioSurgery Division)
Job Type:  Contract
Contract Length:  12-month contract (potential extension or FTE conversion)
Target Start Date:  December/January (2.5 weeks for onboarding timeline)
Work Location/Structure:  Raritan, NJ (Hybrid: 3–4 days onsite)

About the Opportunity:

Our client, a leader in the medical device industry, is looking for a skilled  Senior Packaging Engineer  to join their team for a 12-month engagement. This is a high-impact role that requires a self-motivated professional who can hit the ground running and deliver results quickly.

Key Responsibilities & Deliverables:

This role is focused on the successful completion of specific tasks and deliverables. Your responsibilities will include:

  • Leading packaging development and validation activities for a major packaging redesign project.
  • Developing and executing test methods for new packaging configurations, including performance and stability testing.
  • Collaborating with equipment engineers to define and evaluate equipment and design tolerances.
  • Analyzing data from packaging test labs using Minitab or similar tools.
  • Partnering with cross-functional teams (R&D, Regulatory, Manufacturing, Quality) to maintain design control documentation.
  • Supporting validation of new test equipment installations within the packaging lab.
  • Ensuring all activities align with ISO 11607-1/-2 and J&J quality system requirements.
Required Skills & Experience:

We are looking for someone with a proven track record of successful contract engagements. The ideal candidate will have:
  • 5+ years of relevant experience in medical device packaging or related regulated industry.
  • Deep expertise in test method development, validation, and data analysis. This isn't a learning role—you need to be a subject matter expert.
  • Demonstrated ability to work autonomously and manage your own time effectively to meet project goals.
  • Familiarity with ISO 11607-1/-2, design control, and regulatory submission requirements.
  • Strong communication skills to provide clear and concise status updates to the project team.

DeWinter Group and Maris Consulting  is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. We post pay scales which are based on our client pay ranges. DeWinter, Maris, and our clients have the right to modify the requirements of the role which can impact the pay ranges posted.

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