Manufacturing Process Engineer

3 weeks ago

Enfield, Connecticut, United States Cirtec Medical Full time

Job Summary:

Cirtec Medical is seeking a skilled Manufacturing Engineer II to maintain, develop, and implement cost-effective manufacturing processes and methods in accordance with customer product specifications for components and assemblies to Class III medical device quality standards.

Key Responsibilities:

  • Maintain, develop, and implement cost-effective manufacturing processes and methods in accordance with customer product specifications for components and assemblies to Class III medical device quality standards.
  • Document processes and implement ideas or solutions to improve assembly operations, which may include development of tooling/fixturing as needed to accomplish this task.
  • 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.
  • May 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 coordinate the deployment of changes, including training Operations team members.
  • Perform product and process analysis for cost reduction, quality improvement, and improved efficiency through scrap models and weekly project updates with required actions.
  • Utilize tools associated with risk management (PFMEA/Hazard Analysis) to identify potential risks and the associated corrective actions.
  • Support required equipment installation qualifications, process validations, and retroactive legacy qualifications or validations.
  • Help to determine root cause and implement effective containment and countermeasures.
  • Help to lead Non-Conforming Material Report (NCMR) or customer complaint investigations.
  • Develop, test, and provide ROI cost justification for various tools or equipment recommended for manufacturing.
  • Communicate with customers regarding process improvements and requested production changes.
  • Represent manufacturing on cross-functional teams.
  • Attends, schedules, and may lead project meetings to evaluate current and future process initiatives.
  • Arrange project meetings with customers to discuss current and future process improvements and development initiatives.
  • Complies with company, quality, and safety standards, policies, and procedures.

Requirements:

  • A bachelor-s degree (STEM engineering discipline preferred) and 2 years of experience required; or a combination of education and relevant work experience.
  • Experience in an engineering environment with mechanical, tool design, and manufacturing processes (medical device preferred).
  • Willingness to travel, if required.
  • Must be able to read, write, and speak fluent English.
  • Strong computer skills, including the MS Office suite and MS Project.
  • Must be able to fully interpret technical drawings, blueprints, specifications, and illustrations.

Cirtec Medical Corporation is an equal opportunity employer and welcomes applications from diverse candidates.

Our benefits include training and career development, healthcare and well-being programs, Paid Time Off, and 401(k) retirement savings with a company match.

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