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Sr. Product Development Engineer

Job in Carpinteria, Santa Barbara County, California, 93014, USA
Listing for: Dormont Manufacturing Co
Full Time position
Listed on 2026-07-03
Job specializations:
  • Engineering
    Biomedical Engineer, Product Engineer, Medical Device Industry
Salary/Wage Range or Industry Benchmark: 90000 - 120000 USD Yearly USD 90000.00 120000.00 YEAR
Job Description & How to Apply Below

Working at Freudenberg:
We will wow your world!

Responsibilities:
  • Lead and manage multiple cross‑functional product development projects, ensuring on‑time completion of deliverables while providing technical leadership throughout the product lifecycle.

  • Prepare and lead design/development documentation, such as design input/output records, protocols, reports, and design history files in accordance with ISO, applicable regulatory and company standards.

  • Translate customer requirements, user needs and/or other inputs into clear design requirements, specifications, and design input documentation (as applicable); participate in and lead risk management activities, design/project reviews, and verification testing to ensure product safety and efficacy; apply engineering analysis, design principles, and risk management tools to drive sound design decisions.

  • Develop and evaluate prototypes, generate drawings/specifications, select appropriate materials, develop processes, and collaborate with suppliers to support device design, process development and manufacturing in compliance with regulatory and quality requirements.

  • Lead process characterization and design verification activities, including test method development, fixture design, execution of testing, and documentation of results.

  • Partner with customers/clinicians, marketing, regulatory, quality, NPI/manufacturing, and external experts to develop novel medical devices, assess new technologies/processes, and ensure clinical relevance and manufacturability of designs.

  • Provide engineering support for design/process changes and product launches, resolving technical challenges and driving continuous improvement initiatives.

  • Support audits and compliance activities as a subject matter expert.

  • Participate in intellectual property activities by contributing to invention disclosures, patent strategy discussions, and design differentiation.

  • May be asked to provide input to performance review.

  • Formally train and mentor junior staff, or act as a resource for colleagues with less experience.

  • Support business development activities and opportunities.

  • Strong interpersonal and communication skills dealing with internal and external customers.

Qualifications:
  • Bachelor’s/University degree in Engineering (Mechanical, Biomedical, etc.), or related science/technical field.

  • 8+ years’ experience of engineering in medical device or related industry experience.

  • Extensive knowledge and understanding medical device standards and regulations.

  • Extensive knowledge of GMP principles and their application in medical device manufacturing, including country‑specific regulatory requirements.

  • Knowledge of global regulatory requirements including risk management efforts and thorough risk assessments and mitigation strategies.

  • Experience supporting customer/clinical studies, collecting data, and collaborating with customer/clinicians to ensure compliance with study protocols.

  • Strong familiarity with rapid prototyping techniques.

  • Experience with 3D solid modeling and technical drawings of medical devices desirable.

  • Execution of Design for Manufacturability (DFM) principles and process characterization activities to design and develop products that are manufacturable and cost effective.

  • Strong experience with Project Management (including organizing and facilitating meetings, project planning, balancing multiple projects, and budgeting) and Project management tools (e.g. MS Project).

  • Knowledge of biocompatibility requirements and expertise in selecting appropriate materials for medical device applications and incorporating human factors engineering principles to optimize medical device usability and user experience.

  • Knowledge of IP laws and practices, including patent applications and protection of proprietary technologies.

  • Proven ability to lead cross‑functional teams to achieve project objectives.

  • Leadership skills in establishing and managing comprehensive design control processes, ensuring adherence throughout the product lifecycle.

  • Ability to work independently and also lead small teams in a fast‑paced, results‑oriented environment.

  • Ability to generate complex prototypes using various materials and…

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