Manufacturing Engineer III

Manufacturing Engineer III at Nissha Medical Technologies Manufacturing Engineer III at Nissha Medical Technologies in Colorado Springs, Colorado Posted in 3 days ago. $85,000.00 - $105,000.00 per year

Job Description:

JOB DESCRIPTION

Manufacturing Engineer III About Nissha Medical Technologies Nissha Medical Technologies (NMT) is a global Contract Development and Manufacturing Organization (CDMO) where people, purpose, and technology come together to advance healthcare. Headquartered in the United States, NMT is the medical devices business unit and a wholly owned subsidiary of Nissha Co., Ltd., a publicly traded Japanese company based in Kyoto, Japan (

TSE:

7915). Across our global organization, our teams collaborate to design and manufacture innovative medical devices and solutions that make a real difference in patients' lives. We partner closely with our customers to solve complex challenges, move ideas forward, and support products from concept through commercialization. Our work spans patient monitoring, surgical and interventional solutions, precision components, and emerging technologies, all grounded in a strong culture of quality, accountability, and continuous improvement. At Nissha Medical Technologies, we believe our success is driven by our people. We foster an environment where curiosity is encouraged, teamwork is valued, and individuals are empowered to grow their skills and careers. If you're motivated by meaningful work, collaboration, and the opportunity to help shape the future of healthcare, you'll find a place to belong at NMT. What You Will Do The Manufacturing Engineer III is a technical engineering lead responsible for providing engineering support to manufacturing operations on a routine basis. This positions will develop and improve manufacturing methods, systems and processes to produce a high-quality product at optimal cost. The successful candidate will act under general supervision of the Director of Operations on multiple assignments of moderate scope and complexity, directs and coordinate engineering activities for multiple manufacturing projects and provide support for new product development projects. The ME III may supervise other Engineers and Technicians.

General Duties:

Follow Employee guidelines and Quality System Regulations as defined by Nissha Medical Technologies practices, policies and Standard Operating Procedures to ensure that customer requirements and industry standards and or regulations are met. Demonstrate knowledge and act in accordance with NMT's Employee Guidelines and applicable quality standards as outlined in NMT's Quality Manual. Abide by all safety and security rules set forth by the company and regulatory agencies Regular attendance is required.

Manufacturing Engineering Team Support:

May manage day to day activities of Manufacturing Engineering Team members (engineers or technicians). May monitor Manufacturing Engineering productivity to ensure timely completion of tasks. Provide guidance and coaching to other team members. Set goals for performance in deadlines to align with company plan and vision. Direct and coordinate Manufacturing Engineering team projects.

Production Support and Troubleshooting:

Provide engineering support to manufacturing operations on routine basis. Address product related issues arising on the production floor. Investigate non-conforming materials and products from receiving inspection and the production floor. Initiate and own CAPAs as necessary. Support supplier quality issues and changes in conjunction with the buyer. Customer Support Provide the customer with a dedicated SME for their product line. Implement changes required by the customer and request changes to their production lines as needed. Investigate customer complaints with Quality when necessary.

Continuous Improvement and Cost Reduction:

Continually improve manufacturing methods/systems and process/ product improvements to optimize product performance and reduce manufacturing costs. Identify and evaluate opportunities for improvement and make specific recommendations for adoption. Perform cost analyses to reduce or optimize product costs.

Concurrent Engineering:

Support new product development or existing product line extensions/modifications by ensuring new products or manufacturing processes are designed to facilitate ease of manufacturing and to produce quality, cost effective products with optimized yields. Ensures compliance with GMP's and internal protocol. Uses appropriate statistical support and Design of Experiments (DOE) when developing recommendations.

Equipment and Fixturing:

Determine specific requirements of manufacturing operation in order to specify equipment, fixturing, and process parameters. Collaborate on design with suppliers to fulfill equipment and fixturing requirements.

Qualification and Validation:

Develop plans to evaluate process repeatability and stability through equipment qualification and process validation. Apply appropriate statistical methodologies.

Documentation:

Define and generate all required documentation in support of manufacturing products and processes.

These include:

ECOs, Engineering protocols, FMEAs, reports, manufacturing instructions and procedures. Maintain a high level of documentation that is clear and understandable, contains pertinent and accurate information, and will promote confidence with customers and auditors. What You Bring Core Qualifications Bachelor's degree in engineering A minimum of 5 years of engineering experience in a manufacturing or production environment. Or a minimum of 3 years with an advanced Engineering degree. Experience with CAPA's, MRB's, and/or NCMR's Experience with statistical analysis of Production processes Current or recent experience with equipment and/or process qualifications and validations (IQ,OQ, PQ) Experience writing protocols, reports and engineering change orders Preferred Qualifications Experience designing and conducting DOEs using MiniTab preferred Advanced degree in Engineering preferred Three years of medical device manufacturing or manufacturing in highly regulated environment preferred Experience with quality standards such as

ISO 13485, ISO 14971, FDA 21 CFR

Part 11 preferred Professional Traits We Value Solid interpersonal and communication skills Ability to work in a team environment Problem-solving ability Compensation & Benefits The expected salary range for this position is $85,000 - $105,000 annually. Actual compensation will be determined based on experience, skills, qualifications, and geographic location. In addition, Nissha Medical Technologies offers a competitive total rewards package including medical, dental, and vision coverage, 401(k) with company match, paid time off, life and disability insurance, and professional development opportunities. Equal Opportunity Statement Nissha Medical Technologies is an Equal Opportunity Employer. We are committed to creating an inclusive environment for all employees and applicants and do not discriminate based on any protected status under applicable law.