What are the responsibilities and job description for the Sr. Manufacturing Engineer position at Cirtec Medical Corporation?
About us:
For over three decades, Cirtec Medical has been a leading provider of manufacturing solutions for complex Class II and III medical devices. We specialize in providing comprehensive services from design and development to manufacturing and finished device assembly. Our expertise spans active implants and neuromodulation, interventional cardiology, structural heart, minimally invasive surgical systems, smart orthopedics, and precision components.
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 challenge, you may be a perfect fit for our team!
Position Summary:
This position is primarily responsible for maintaining, developing, and implementing robust cost-effective
manufacturing processes and methods in accordance with customer product specifications for
components and assemblies to Class III medical device quality standards. Manufacturing Engineers
document processes and could implement creative ideas or solutions to improve assembly operations
which may include development of tooling/fixturing as needed to accomplish this task.
Key Responsibilities:
- Implement, plan, and execute continuous improvement projects for cost reduction, quality
improvements and efficiency from conception to fully established production. - Improve manufacturing process instructions, product flow, assembly methods, space allocation, product quality and safety performance.
- Help product development with the manufacturing launch of new products including evaluating yield targets, run rates, training needs and quality results.
- Prepare engineering change orders and coordinates the deployment of changes including training Operations team members.
- Perform product and process analysis for cost reduction, quality improvement and improved
efficiency. - Utilize tools associated with risk management (PFMEA/Hazard Analysis) to identify potential risks and the associated corrective actions.
Must Have:
- A Bachelors degree (STEM engineering discipline preferred) and 5 years of experience required.
- Experience in an engineering environment with mechanical, tool design, and manufacturing
processes - Must be able to read blueprints and interpret technical specifications and illustrations.
Good to have:
- Previous experience with Class III Medical devices, FDA standards, ISO 13485 and GMP
principles preferred.
Competitive market salary from $93,000 to $138,500 per year depending on qualifications and experience.
Cirtec Medical Corporation considers everyone 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 its related companies fully endorse equal opportunity. 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 Cirtecs goal to create an enjoyable 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 stage of your career and life. 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.
Salary : $93,000 - $138,500
