Manufacturing Engineer

Company Description Contract Medical Manufacturing (CMM) specializes in manufacturing and assembling medical devices to customer specifications in full compliance with FDA and ISO 13485:2003 requirements. The company operates in a quality-driven environment focused on delivering high-quality products at cost-effective prices. CMM supports both medical and non-medical device customers, applying its expertise to a wide range of specialized requirements. Team members contribute directly to ensuring that products meet rigorous regulatory standards and customer expectations.

Role Description This is a full-time, on-site Manufacturing Engineer role based in Oxford, CT. The Manufacturing Engineer will design, develop, and optimize manufacturing processes and workflows to support medical device production in compliance with FDA and ISO standards. Day-to-day responsibilities include analyzing production data, identifying process improvements, developing work instructions, and collaborating with quality, engineering, and operations teams to resolve technical issues. The role involves supporting equipment selection and validation, assisting with tooling and fixture design, and providing hands-on support on the shop floor to ensure safety, efficiency, and product quality. The Manufacturing Engineer will also participate in continuous improvement initiatives, cost-reduction projects, and documentation updates to maintain robust manufacturing systems.

Qualifications

• Candidates should possess strong knowledge of Manufacturing Engineering and Manufacturing Processes, including process development, optimization, and troubleshooting.


• Candidates should possess skills in Mechanical Engineering and Machining, with the ability to understand component design, tolerances, and fabrication methods.


• Candidates should possess competencies in Industrial Engineering, such as workflow analysis, layout optimization, and productivity improvement.


• Bachelor’s degree in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering, or a related technical field.


• 3-5 years experience in regulated manufacturing environments; medical device or FDA/ISO 13485


• Ability to read and interpret technical drawings, specifications, and work instructions.


• Strong problem-solving, analytical, and root-cause analysis skills with attention to detail.


• Effective communication and collaboration skills to work with cross-functional teams on-site.


• Proficiency with common engineering tools and software (e.g., CAD, ERP/MRP systems, basic data analysis tools).

Pay & benefits

• pay rate - $75,000 - $90,000


• Dental, Life insurance, Medical, PTO, Retirement, Vision