Job Information
Cirtec Medical Process Development Technician II in Enfield, Connecticut
Process Development Technician II
Department: Development Engineering
Location: Enfield, CT
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This position is located on-site based out of Enfield, CT.
ABOUT THE COMPANY
Cirtec Medical is more than just another design shop or contract manufacturer, we offer a uniquely comprehensive range of vertically integrated capabilities. Cirtec Medical specializes in complex, difficult to produce components and devices in today-s most advanced product technologies including, neuromodulation, implantable drug delivery, cardiac rhythm management, ventricular assist and interventional devices and delivery systems. We have the capabilities needed to bring products to full production, including assembly, packaging and testing, and in-house sterilization.
Our employees have the expertise needed to design innovative devices, solve complex design challenges, and help bring our customers- devices to market. If you are interested in working in a fun, challenging, fast-paced environment with a company that is growing and providing leading edge technology, Cirtec is the company for you!
You are a part of:
The Engineering team consists of engineers with diverse backgrounds and expertise. The Engineering team works in close collaboration with Operations, R&D, and Purchasing. You will be involved in the design, development, documentation and validation of new customer products, and modification of existing products including defining requirements, timelines, and deliverables with a focus on prototypes, process development, design verification, clinical builds, training production, and preparation for process validation and manufacturing transfer of products.
JOB SUMMARY
The Technician II, Process Development is primarily responsible for providing tools and support to
engineering and production while adhering to the quality and cost requirements of the company. The tools
included but are not limited to written processes and procedures, equipment and fixtures, and training
programs. The development of these tools must be based on sound engineering principles and be
implemented in accordance with Good Manufacturing processes (GMP) and ISO standards. This position
will also support other engineers and areas as needed and performs at an advanced level.
ESSENTIAL RESPONSIBILITIES
Identifies, executes, and promotes Continuous Improvement objectives
Assists in defining Lean Manufacturing requirements
Develop processes and procedures for projects to improve quality and cost
Originate and maintain written technical descriptions of processes and procedures comprehensive in scope and understandable by the audience
Represent engineering for Material Review Board concerning material dispositions
Represent Engineering in cross functional teams as assigned
Maintain compliance to procedures and regulatory requirements
Understand and follow safety policies and practices, attend safety training and wear PPE as required
Maintains and prepares project plans to satisfy timeline requirements
Prepares Engineering Change Orders for processes and components
Performs Corrective and Preventative Action tasks
Reliable, consistent, and punctual attendance is an essential function of the job
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.
QUALIFICATIONS
Bachelor-s degree in related technical field
3 Plus years- experience in the engineering/manufacturing environment for medical devices
FDA, cGMP principles and practices, (ISO 9001, ISO 13485)
Experience with Silicone molding is a plus
Familiarity with Pro-E / CREO and or SolidWorks is preferred.
Strong computer skills associated with Microsoft software
Ability to interpret technical drawing, blueprints, specification, and illustrations
Must be able to read, write and speak fluent English.
Excellent reading, writing, communication, and organizational skills.
Demonstrated ability for systematic problem solving, DMAIC
WHAT WE OFFER
A fast-paced work environment
Paid time off
401(k) retirement savings with a company match
Clean, and well-lit production areas
Training and career development, with onboarding programs for new employees and tuition assistance
Financial security through competitive compensation, incentives and retirement plans
Health care and well-being programs including medical, dental, vision, wellness and occupational health programs
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.
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