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Sr. Mechanical Engineer (Must Have Test Method Development, Verification, Medical Device)

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Onsite

Sr. Mechanical Engineer (Must Have Test Method Development, Verification, Medical Device)

MillenniumSoft Inc

Sr. Mechanical Engineer (Must Have Test Method Development, Verification, Medical Device)

Skills

RCompliance

2 months ago

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Important information


Contract type:

Permanent

Location:

Franklin Lakes, NJ, USA

Work mode:

Onsite

Published on:

27 August 2026

What they need


Position: Sr. Mechanical Engineer (Must Have Test Method Development, Verification, Medical Device) Location: Franklin Lakes, NJ Duration: 12+ Months Contract **Total Hours/week: 40.00

pay rate-$45-50/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 The R&D Test Method Development, Verification & Validation ("TMD / VnV") team within Client Medical - Medication Delivery Solutions (MDS) is seeking a highly talented and passionate individual to help the team identify innovative solutions to address current and future health care needs in the medication delivery markets.

The incumbent will join as a Contract Engineer, requiring moderate oversight and providing technical leadership and support to a cross-functional team. The successful candidate will be responsible for: supporting product verification activities; contributing to - and possibly leading - test method development activities; measurement system development, analysis and qualification; test fixture design; creation and execution of design verification strategies required for sustaining existing and commercialization of various types of new medical device products used in drug delivery.

The ideal candidate will plan and participate in executing technical and cross-functional project work which may include all phases of product development, including: design and development planning; requirements definition; product development; root cause analysis; test method development; and design verification/validation. Additionally, the candidate will be expected to participate in the development of new technologies for testing products that will help meet current and future clinical unmet needs.

Responsibilities Specific responsibilities will include the following as well as other duties as assigned:

  • Provide technical direction and oversight of V&V test method development activities. Define, plan and lead activities, including, test method & measurement system development and validation, fixture design and testing optimization in support of Design Verification.
  • Participate in the planning and execution of technical project work. This will involve the application of engineering first principles and advanced engineering methods to gain deep understanding of the underlying technical issues, and to propose and implement robust solutions.
  • Collaborate with Systems and Engineering teams to understand and derive specifications for a broad portfolio of MDS products.
  • Create and document novel test methodologies and provide feedback and recommendations for product/design changes.
  • Resolve technical problems. Identify or create solutions for technical problems using systematic problem-solving and statistical methodologies.
  • Support project plan development and contribute to the development of the Design Verification strategy.
  • Conduct and encourage frequent formal and informal communication with the team to ensure full engagement and efficient operation.
  • Expected to mentor associates in related technical roles. Provide technical direction and frequent feedback.
  • Developing personal skills, expertise, and competencies. Ensure that technical lessons are reviewed, learned, and disseminated.
  • Ensure compliance with BD quality policies, procedures, and practices.
  • Ensure compliance with all local, state, federal, and Client safety regulations, policies, and procedures

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