Technician I, Engineering

BP – Engineering        ·      Brooklyn Park, MN       ·        Full time

This position is eligible for a $3,000 sign on bonus.  

Job Summary

This position is primarily responsible for utilizing state of the art equipment for the development of life changing medical devices. The ideal candidate will be comfortable operating a variety of equipment including, but not limited to; lasers, injection molders, reflow machines as well as an array of test equipment while adhering to the quality requirements of the company. In addition, this position will work with the design and process teams to ideate, create, and build first prototypes. This individual is essential in the maturation of these prototypes and their progress through the development. Lastly, the technician must feel comfortable providing candid feedback to the development team to ensure success in later phases of the program.

Essential Responsibilities

• Comply with all Good Manufacturing Practices (CGMP) requirements to ensure products are consistently produced and controlled according to the Quality System.
• Complies with company, quality and safety standards, policies and procedures
• Run equipment tests, collect data and analyze data with the engineering team.
• Make recommendations on how to improve the quality or efficiency of a process based on data and observation.
• Ability to diagnose and solve problems with jobs in a timely manner.
• Assist in training employees on equipment and assembly skills.
• Interact effectively and assist engineering in improving quality and solving problems.
• Develop processes and procedures for projects to improve quality and cost.
• Originate and maintain written technical descriptions of processes and procedures comprehensive in scope and understandable by the audience.
• Represent engineering for Material Review Board concerning material dispositions.
• Represent Engineering in cross functional teams as assigned.
• Maintain compliance to procedures and regulatory requirements.
• Understand and follow safety policies and practices, attend safety training and wear PPE as required.
• Prepares Engineering Change Orders for processes and components.
• Performs Corrective and Preventative Action tasks.
• Complies with company, quality and safety standards, policies, and procedures
• Other duties as assigned. An individual in this position must be able to successfully perform the essential duties and responsibilities listed above. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position. Rev. 3/1/2021

Qualifications

• High school diploma or G.E.D. Certificate required
• Two-year technical degree in Engineering preferred
• Strong drive to learn, share and teach
• Understanding of and experience with mechanical equipment
• FDA, cGMP principles and practices, (ISO 9001, ISO 13485)
• 3 Plus years’ experience in the engineering/manufacturing environment for medical devices
• In-depth understanding of one or more manufacturing processes is a plus
• Familiarity with Pro-E / CREO and or SolidWorks is preferred.
• Strong computer skills associated with Microsoft software
• Ability to interpret technical drawing, blueprints, specification and illustrations
• Must be able to read, write and speak fluent English.
• Excellent reading, writing, communication, and organizational skills.
• Maintains performance with changing priorities under minimal supervision
• Possess strong team collaboration skills
• Must be able to make clear and accurate decisions
• Strong desire to learn and apply new technology

Working Environment

Work is performed in an office environment. The noise level in the work environment is usually moderate. The work environment characteristics described here are representative of those an individual encounters while performing the essential functions of this position.

If you are an individual with disabilities who needs accommodation or you are having difficulty using our website to apply for employment, please contact one of the the locations below:

MN: Kim Dickey 763-493-8556 Ext. 55762 or Kim.Dickey@cirtecmed.com
CT: Cheryl Walker 860-814-3962 or Cheryl.Walker@cirtecmed.com
CA & AZ: Claire Buchanan 763-493-8556 Ext. 55702 or Claire.Buchanan@cirtecmed.com
MA: Melinda Polleck 978-703-6822 Ext. 66911 or Melinda.Polleck@cirtecmed.com

Please click here to apply.