Job Opening for Engineer I Process Development in Cirtec Medical (99 Print Shop Rd, Enfield, CT 06082)

Responsibilities:
Attends and arranges project meetings to discuss current and future design and development initiatives.
May serve as primary contact with customers on programs of low complexity and serve as secondary contact with customers on programs of low to moderate complexity.
Track and communicate the status of assigned action items that would affect timelines and budgets.
Assist in the preparation and maintenance of project plans to satisfy milestones, deadlines, budgets, and medical device quality regulations with required actions. Provide input to program management for tracking and communicating project status, plans, issues, timelines, action items, and budgets.
May have responsibility for any of the following project inputs:
Feasibility builds, documentation, root cause analysis, and testing
Equipment selection and qualification
Process development and documentation
Device Verification samples and testing
Operator training
Process Failure Mode Effects Analysis
Clinical builds
Process Validation
May be involved in the full design, development, and validation requirements of programs, including:
Product design and specification creation, including mechanical and electrical components, assemblies, and packaging.
Materials sourcing and device prototyping.
Design verification and validation activities, including data for regulatory submission.
Manufacturing transfer and support of existing product lines as applicable.
Reliable, consistent, and punctual attendance is an essential function of the job.
Other duties as assigned.

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.

Qualifications:
A Bachelor’s degree in an engineering discipline.
Experience in an engineering environment with mechanical, tool design, and manufacturing processes preferred.
Willingness to travel, if required.
Must maintain high ethical standards.
Must demonstrate good organizational skills.
Must be able to read, write and speak fluent English.
Strong computer skills, including MS Office.
Experience with Minitab and statistical analysis preferred.
Experience with documented change control processes preferred.
Must be able to fully interpret technical drawings, blueprints, specifications & illustrations.
Strong analytical skills, must be able to obtain, evaluate, and apply secondary research information.
Ability to learn and apply new technology.
Technical report preparation and small group presentation skills.

WORKING ENVIRONMENT

Work 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 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 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.