Full-Time

Associate Principal Scientist

Device Product and Process Development, Associate Director Equivalent

Posted on 5/13/2025

Deadline 5/14/25
Inventing for Life

Inventing for Life

Compensation Overview

$139.6k - $219.7k/yr

+ Bonus + Long Term Incentive

Senior

H1B Sponsorship Available

Linden, NJ, USA

Hybrid work model consisting of three total days on-site per week, Monday - Thursday, with Friday designated as a remote-working day.

Category
Veterinary Professionals
Medical, Clinical & Veterinary
Required Skills
Risk Management
SolidWorks
Requirements
  • Ph.D. in Mechanical Engineering or equivalent field is required.
  • A minimum of a Ph.D. plus 4 years of device design and engineering evaluation experience.
  • Fluency in structural finite element analysis (FEA).
  • Solid testing and troubleshooting skills able to work independently in a laboratory setting.
  • Experience with mechanical testing, imaging, and measurement equipment and techniques. Including, but not limited to, mechanical testing, surface characterization, x-ray computed tomography, rheometry, and microscopy.
  • Experience in 3D CAD (e.g. Solidworks), geometric tolerancing and stack-up analysis.
  • Fluency in Design Failure Modes and Effect Analysis (FMEA, DFMEA).
  • Cross-functional communication – communicating complex mechanical engineering information in layman’s terms to facilitate cross-functional understanding and to support project timelines.
  • Development experience in risk-oriented, regulated environments.
  • Development project leadership with a proven track record collaborating with and managing external vendors/research partners.
Responsibilities
  • Technical interrogation of the various drug delivery device technology platforms to identify risks and opportunities for improvement.
  • Utilize a wide variety of cutting-edge analytical instruments and methods, including *in silico* modeling, to build fundamental understanding of the devices’ material and functional properties and attributes.
  • Design and develop functional improvements for drug delivery platforms.
  • Develop new and novel delivery technologies as opportunities arise.
Desired Qualifications
  • Experience with medical device development with understanding of Design Controls (21 CFR 820.30)
  • Familiarity with the following standards: Quality Management – ISO 13485, Risk Management – ISO 14971, EU MDR, ISO 11608 Needle-based injection system for medical use.
  • Familiarity with Design Verification (DV) strategies and mechanical tests with validations, including engineering studies, design verification protocols, stability studies and validation protocols, ensuring appropriate selection of acceptance criteria and sampling plans. Ensures measurement systems analysis (MSA’s) for all finished product performance test methods as needed in tech transfer or lifecycle.
  • Additional familiarity/experience with the following knowledge is a plus: 21 CFR Part 4, 21 CFR 211, FDA Guidance for Industry, Container Closure Systems for Packaging Human Drugs & Biologics, ISO 13485, ISO 14971, ISO 11040, ISO 10993.

Company Size

N/A

Company Stage

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Total Funding

N/A

Headquarters

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Founded

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INACTIVE