New

Process Development Technician I

Cirtec Medical
paid time off, 401(k)
United States, Connecticut, Enfield
99 Print Shop Road (Show on map)
Jun 19, 2026
Description About us: For over three decades, Cirtec Medical has been a leading outsourcing partner for complex medical devices. We specialize in providing comprehensive solutions for Class II and III devices, from design and development to precision components and finished device assembly. Our expertise spans neuromodulation, implantable drug delivery, cardiac rhythm management, structural heart, mechanical circulatory support, and minimally invasive surgical systems. Our dedicated teams prioritize growth, innovation, and collaboration. We actively seek opportunities for improvement to enhance our support for clients. If you embrace a growth mindset and thrive on challenges, you may be a perfect fit for our team! Position Summary: Process Development Technician I is primarily responsible for providing tools and support to engineering and production while adhering to 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. Key Responsibilities: Identifies, executes and promotes Continuous Improvement objectives Assist 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 Must Have: Highschool diploma or General Education Degree (GED) is required 3+ years' experience in the engineering/manufacturing environment for medical devices FDA, cGMP principles and practices, (ISO 9001, ISO 13485) Must be able to read, write and speak fluent English Good to have: Familiarity with Pro-E/CREO and SolidWorks Demonstrated ability for systematic problem solving, DMAIC Excellent reading, writing, communication, and organizational skills. 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. We work to create a culture that is built on innovation, respect, transparency and communication, and hope you take pride in being a member of our team. It is Cirtec's goal to create a great work environment and to keep the company a great place to work. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Our benefits include Training and career development, Healthcare and well-being programs including medical, dental, vision, wellness and occupational health programs, Paid Time Off and 401(k) retirement savings with a company match.