Engineer II, Applications

The Engineer II, Applications is primarily responsible for generating proposals for engineering projects involving mechanical devices, value-added assemblies, and high-precision components. The Applications Engineer will also support other Applications Engineering staff with the collection and organization of cost data for complex development proposals.ESSENTIAL RESPONSIBILITIESCollaborates with cross-functional engineering teams to assess and document technical development plans, incorporating knowledge of both existing and new assembly processes and techniques.Applies engineering skills and know-how to evaluate and recommend technical solutions to customer development requests.Participates in the definition of requirements, scope, timeline, and budget for new development programs. Supports others in the development of budgetary project plans, development proposals, and quotations for both new and existing customers.Writes proposals for development programs with clear technical communications skills using a variety of visual and written techniques (e.g., graphs, diagrams, long-form writing).Gathers peer review on written proposals and participates in management reviews of the proposals to get required approvals.Participates in continuous improvement of Cirtec’s design control procedures and internal business processes.Communicates with vendors and suppliers for sourcing and development of new components.Analyzes internal manufacturing and supply chain data to assess actual costs and estimate future production costs.Other duties as assigned.This is not a remote position.An individual in this position must be able to successfully perform the essential duties and responsibilities listed above. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.QUALIFICATIONSBS 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 ENVIRONMENTWork is performed in an office environment. The noise level in the work environment is usually moderate. The work environment characteristics described here are representative of those an individual encounters while performing the essential functions of this position.EEO STATEMENTCirtec 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 Corporation and all of its related companies fully endorse equal opportunity for all. Cirtec Medical provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in the job application process.

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