Demo

Staff Engineer R&D

embecta
Andover, MA Full Time
POSTED ON 8/19/2024 CLOSED ON 9/18/2024

What are the responsibilities and job description for the Staff Engineer R&D position at embecta?

embecta is one of the largest pure-play diabetes care companies in the world, leveraging its nearly 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of approximately 2,000 employees around the globe. For more information, visit embecta.com or follow our social channels on LinkedIn, Facebook, Instagram and Twitter.

Lead and contribute to the creation and development of complex electro-mechanical systems by applying technical rigor for the innovation, creation and development of R&D and development programs to address the current and future needs of medical device products that improve the safe delivery of therapeutic drugs.

Responsibilities

  • Assume the role as SME (Subject Matter Expert) for electro-mechanical architecture or major subassemblies.
  • Lead the application of rigorous component, subsystem and system evaluation using first principles thinking and engineering analysis tools such as FEA and tolerance simulations.
  • Lead and manage internal and external stakeholders related to project activities.
  • Oversee the development of production and process documentation, prepare technical analysis, and recommend strategic work related to new or improved products and processes.
  • Provide mentoring to junior engineers.
  • Assign technical and/or cross-functional project work.
  • Manage the development and execution of test methods which specify measurement equipment, test set-up, measurement system analysis, and data analysis.
  • Contribute to a culture of innovation by proactively generating novel concepts for new products and enhancements to current product performance.
  • Understand customer needs through literature review, customer interviews, direct observation, competitive analysis, prototype evaluation, and clinical/simulated use studies.
  • Translate customer needs into engineering requirements for detailed product, packaging, and process specifications.
  • Create, develop, and release engineering drawings into a controlled documentation system.
  • Document and write detailed technical reports based on design verification analysis/testing for all engineering activities.
  • Ensure compliance to embecta quality policies, procedures, and practices as well as with all local, state, federal and embecta safety regulations, policies, and procedures.
  • Any other tasks as assigned by your manager.
  • May require up to 15% travel.

Experience & Education

  • BS or MS degree in engineering is required (Mechanical or Biomedical preferred).
  • Experience: 8 years of engineering experience is required, preferably in medical devices. 10 years and MS preferred.

embecta is an Equal Opportunity/AffirmativeAction Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
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