Process Development Manufacturing Engineer Jobs in Connecticut

Description

Senior Manufacturing Engineer 

Full-time | Permanent

Salaried | On-site

*We are not currently working with third party agencies on this role.

About Us:

Hobson & Motzer is now part of Vantedge Medical! Vantedge Medical is the premier metals-based med-tech solutions partner from concept to full-scale manufacturing. We are at the forefront of precision engineering and innovation, specializing in the development and manufacturing of vital components for medical markets such as Robotic Assisted Surgery, Orthopedics, Surgical Instruments, Dental, and more. Our teams work in unison, collaborating and problem-solving to serve the manufacturing needs of the top Medical Original Equipment Manufacturers (OEMs) around the globe. Making a difference in the lives of patients and their families drives us to go above and beyond every day. With a steadfast commitment to advancing medical technology, we take immense pride in the work we do - and have a lot of fun doing it. 

About this Opportunity:

We are seeking a process oriented and results-driven Manufacturing Engineer III to lead process and new product quote development in a medical device contract manufacturing environment at our Hobson Motzer Durham, CT site. The primary responsibility of this position is to apply high-level engineering principles to drive process development, costing, and improvements in the manufacturing of medical devices to positively affect Quality, Delivery, Cost, Safety and Morale. Additionally, this position will be responsible for executing projects with limited supervision. We are looking for someone with a positive attitude and attention to detail who wants to grow professionally with high internal expectations.

This role supports base business improvement and/or new product launches, develops progressive die tooling, machining fixtures, gage and measuring fixtures, implements lean methodology, investigates issues using root cause analysis, implements improvements, manages CAPAs, and creates documentation such as standard work and validation protocols. Additionally, they will lead quoting efforts for new business opportunities by reviewing prints, determining efficient processes for manufacturing, identifying part and project risks, proposing DFM, and generating pricing through use of quote tools. They will be responsible for completion of quotes and will be a critical person to provide technical. This position will collaborate cross-functionally to optimize designs for manufacturability, cost, and communicate effectively with internal teams and customers. 

Responsibilities:

1. Base Business and NPI Engineering:

• Adheres to all safety and quality requirements including but not limited to: Quality Systems, U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements.
• Creates and implements lean processes in a cellular environment utilizing appropriate methods such as metals machining, sheet metal fabrication, and sub-processing such as assembly, powder coat, and metal finishing, welding, laser cutting, and electrical harness assembly.
• Performs root cause analysis to identify and implement needed process improvements eliminating waste
• Defines, produces and implements documents including standard work and process work instructions.
• Identifies, develops, justifies, and executes detailed project plans for engineering work with minimum supervision.
• Ability to launch new products effectively in a contract manufacturing environment.
• Investigates, develops and implements new process technologies.
• Successfully communicates complex issues with customers and internal team members.
• Creates, reviews and approves engineering drawings, equipment layouts, change orders and specifications.
• Develops tooling, fixtures and equipment used in manufacturing to optimize productivity and cost.
• Effectively owns and manages CAPAs pertaining to their areas of responsibility.
• Collaborates with development, programmers, machinists and suppliers to evaluate designs for manufacturability and cost reduction.
• Creates and executes validation protocols, processes and material evaluations.

2. Costing Engineer:

• Develop costing for new business opportunities across multiple sites to support small-format machining.
• Collaborate with company SMEs to determine optimal approaches for processes, machine cycle times, equipment selection, fixture design, and automation.
• Identify, document and communicate to the customer DFM opportunities to positively impact cost, quality, and delivery.
• Partner with Commercial to provide technical support when delivering customer proposals to build confidence in the manufacturing process quoted.
• Investigates new technologies and capabilities, with a focus on improving competitiveness in cost structure to increase value to customers and our business.

The successful candidate will:

• Plan and execute projects, with minimum supervision, on time and within budget to achieve tangible results.
• Drive improvements through root cause analysis and data driven decision-making.
• Participates in cross-functional project teams to propose and implement creative solutions.
• Ensure internal and external customer expectations are met or exceeded.
• Develop accurate quotes with a strategic mindset of how to best serve the customer and the business
• Conduct cost benefit analysis in preparation for projects or quotes.
• Calculate material, labor, and overhead costs.
• Manage assigned quotes to ensure timely completion.

Requirements

• Engineering or bachelor's degree in a technical field.
• 7+ years of work experience in similar technical roles including medical device manufacturing required
• Strong problem-solving skills.
• Ability to provide solid rational and justification for process proposals and improvement change requests
• Lean manufacturing and new product development or launch support experience is highly desirable.
• Understanding of metals machining, sub-processing, assembly, and inspection is strongly preferred.
• Ability to collaborate in a team environment.
• Strong written and oral communication skills.
• Experience in medical devices is preferred.
• Proficiency in Microsoft Office Suite
• Working knowledge of ISO and FDA regulations and GD&T

Working Conditions

• Full-time on-site position
• Infrequent travel as needed for site-visits, customer meetings, and industry events