2 Engineering jobs in Boise

NPI Project Engineering Manager

83605 Caldwell, Idaho Molex

Posted 8 days ago

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Job Description

Permanent
Your Job

Phillips Medisize is seeking anNPI Project Engineering Managerto lead our New Product Introduction teams in Phoenix, AZ and Caldwell, ID. As the NPI Project Engineering Manager, you will be responsible for introducing new products at two the campuses. In this role you will have responsibility for the NPI team as well as be the primary contact for our customers.

This is an onsite position that can be based in either Phoenix, AZ or Caldwell, ID.

Our Team

At Phillips Medisize, our goal is to create value for others. We empower every team member to hear, feel and see the quality in every action we take. By incorporating quality into the design of products and processes and predicting potential quality problems before manufacturing and delivering the product, we can create mutual benefit.

What You Will Do

  • Provide leadership and direction to the NPI Engineering team, including people management functions (performance management, recruiting, hiring, career development) and ensuring alignment with team goals
  • Oversee engineering activities, including project coordination, cost estimating, and development of automated solutions to meet program expectations
  • Plan and implement new manufacturing processes and improvements for current and future production lines
  • Lead problem-solving initiatives, such as lean manufacturing and six sigma projects, to optimize process flows and drive efficiency
  • Manage projects from initiation through completion, including planning, quoting, and execution to ensure objectives are met
  • Foster effective communication across internal and external stakeholders, including customers, departments, and broader teams
  • Facilitate collaboration between quality, engineering, and operations to ensure seamless project integration
  • Stay informed on emerging technologies and best practices in manufacturing to enhance facility operations
  • Proactively identify and address safety concerns, integrating safety systems into manufacturing processes

Who You Are (Basic Qualifications)

  • Five (5) years or more experience in New Product Introduction and project management
  • Three (3) years or more supervisory or leadership experience, preferably in a regulated manufacturing environment
  • Demonstrated knowledge of engineering systems and processes, with experience using project management tools, methodologies, and practices

What Will Put You Ahead

  • Bachelor's degree in engineering or a related field
  • Experience in FDA-regulated medical device manufacturing, with a strong focus on process control equipment and compliance standards
  • Expertise in defining and developing manufacturing solutions, including robotics and automated systems, to enhance efficiency and quality
  • Knowledge of fiber optics, tooling, materials, product design, and related processes, including secondary operations and automation technologies

In order to comply with U.S. export control laws and regulations, this position requires applicants to either provide proof of U.S. citizenship or lawful permanent resident status or be eligible to receive an export authorization (a license) under the International Traffic in Arms Regulations and/or the Export Administration Regulations.

At Koch companies, we are entrepreneurs. This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions. Any compensation range provided for a role is an estimate determined by available market data. The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location. If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.

Hiring Philosophy

All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds. We are Military Ready and Second Chance employers. Learn more about our hiring philosophy here .

Who We Are

As a Koch company, Molex is a leading supplier of connectors and interconnect components, driving innovation in electronics and supporting industries from automotive to health care and consumer to data c ommunications. The thousands of innovators who work for Molex have made us a global electronics leader. Our experienced people, groundbreaking products and leading-edge technologies help us deliver a wider array of solutions to more markets than ever before.

At Koch, employees are empowered to do what they do best to make life better. Learn how our business philosophy helps employees unleash their potential while creating value for themselves and the company.

Our Benefits

Our goal is for each employee, and their families, to live fulfilling and healthy lives. We provide essential resources and support to build and maintain physical, financial, and emotional strength - focusing on overall wellbeing so you can focus on what matters most. Our benefits plan includes - medical, dental, vision, flexible spending and health savings accounts, life insurance, ADD, disability, retirement, paid vacation/time off, educational assistance, and may also include infertility assistance, paid parental leave and adoption assistance. Specific eligibility criteria is set by the applicable Summary Plan Description, policy or guideline and benefits may vary by geographic region. If you have questions on what benefits apply to you, please speak to your recruiter.

Additionally, everyone has individual work and personal needs. We seek to enable the best work environment that helps you and the business work together to produce superior results.

Equal Opportunities

Equal Opportunity Employer, including disability and protected veteran status. Except where prohibited by state law, some offers of employment are conditioned upon successfully passing a drug test. This employer uses E-Verify. Please click here for additional information. (For Illinois E-Verify information click here , aquí , or tu ).

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REMOTE Senior Supplier Quality Engineering

Meridian, Idaho GForce Life Sciences

Posted today

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Job Description

part-time
Summary Our client, an innovative global leader within medical devices, has engaged GForce Life Sciences to provide a Senior Supplier Quality Engineer (SQE). The senior SQE will strategize and establish a baseline for supplier quality processes and turn over the QMS. Draft & Implement process and procedure changes for more efficient execution while enhancing regulatory requirements.
Lead Continues Improvement initiatives to streamline operations and transfer activities br> Lead and support supplier transfer activities, including validation of transferred processes, equipment, and measurement systems.
Lead Part Production Approval Process (PPAP) and ensure alignment of supplier validation and qualification deliverables.
Collect, review, and archive supplier documentation required for qualification, validation, and monitoring activities.
Ensure robust validation protocols and reports are executed in alignment with regulatory and internal quality standards.
Facilitate cross-functional collaboration with Engineering, Manufacturing, and Supply Chain during supplier transitions and process transfers.
Assess and propose appropriate measurement systems to ensure capability and repeatability in manufacturing and supplier processes.
Provide on-site support and oversight during manufacturing transfers, including presence on the manufacturing floor to evaluate processes, equipment setup, and operator readiness.
Review and acknowledge supplier notifications, verify content, and request additional information (scope, change description, supportive data) as needed.
Draft and manage Change Request Forms (CRFs) based on supplier notification details; Support supplier quality contracts and technical agreements by reviewing content, requesting clarifications, and facilitating negotiations with suppliers.
ensure compliance with quality system requirements.
Track supplier remediation actions (containment, root cause analysis, corrective and preventive action) and ensure timely closure of SCARs and nonconformances.
Support supplier performance monitoring and quarterly reviews with consolidated reporting on validation and transfer activities.
Bachelor of Science in Engineering or related technical discipline
~8+ years of experience in supplier quality within the medical device industry
~ Strong experience in validation activities (process, equipment, and/or measurement system validation)
~ Hands-on experience or exposure to manufacturing floor processes
~ Familiarity with PPAP, supplier change control, and regulatory requirements (ISO 13485, FDA, etc.)
~ Excellent problem-solving, communication, and technical writing skills


Onsite in Olive Branch, MS (3x/week first few months then flexible) highly preferred, remote is possible
~8-12 month contract
~ Start ASAP
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