Senior Applications Engineer

3 days ago

Lowell, Massachusetts, United States Cirtec Medical Full time
Job Summary

The Applications Engineer II is a key member of our engineering team, responsible for generating proposals for engineering projects involving mechanical devices, value-added assemblies, and high-precision components. This role requires strong technical skills, excellent communication abilities, and a keen eye for detail.

Key Responsibilities
  • Collaborate with cross-functional engineering teams to assess and document technical development plans, incorporating knowledge of existing and new assembly processes and techniques.
  • Apply engineering skills and know-how to evaluate and recommend technical solutions to customer development requests.
  • Participate in the definition of requirements, scope, timeline, and budget for new development programs.
  • Support others in the development of budgetary project plans, development proposals, and quotations for both new and existing customers.
  • Write proposals for development programs with clear technical communications skills using a variety of visual and written techniques.
  • Gather peer review on written proposals and participate in management reviews of the proposals to obtain required approvals.
  • Participate in continuous improvement of Cirtec-s design control procedures and internal business processes.
  • Communicate with vendors and suppliers for sourcing and development of new components.
  • Analyze internal manufacturing and supply chain data to assess actual costs and estimate future production costs.
Qualifications
  • BS in Biomedical / Mechanical / Electronics / Computer engineering discipline with at least 3 years of experience within the medical device industry.
  • Must have experience working on medical device development projects from design through transfer to production.
  • 3+ years- experience in the engineering / manufacturing environment of medical device component assembly.
  • Experience with active implant devices or implantable components preferred.
  • Must possess strong understanding and working knowledge of ISO 13485 and FDA 21CFR820 based Quality Systems and Design Control.
  • Must be able to interpret technical drawings, product requirements, design specifications, and relevant technical documents.
  • Must have proficiency in MS Office software.
  • Must be able to read, write, and speak fluent English.
  • Must possess excellent written and oral communication skills in English.
  • Willingness to travel, if required.
Working Environment

Work is performed in an office environment. The noise level in the work environment is usually moderate.

EEO Statement

Cirtec Medical Corporation is an Equal Opportunity Minority/Female/Individuals with Disabilities/Protected Veteran and Affirmative Action Employer.

Cirtec Medical Corporation considers for employment and hires qualified candidates without regard to age, race, religion, color, sex, sexual orientation, gender identity, national origin, ancestry, protected veteran or disability status or any factor prohibited by law.

Cirtec Medical provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in the job application process.

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