Getinge Job - 34285470 | CareerArc
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Company: Getinge
Location: Merrimack, NH
Career Level: Mid-Senior Level
Industries: Healthcare, Pharmaceutical, Biotech

Description

Job Functions:

  • Modify and improve existing equipment.  Improve manufacturing efficiency, production yields, product quality and consistency through equipment and product design modifications and fabrication.
  • Finalizes manufacturing methods for medical devices.
  • Responsible for process validation.
  • Provide assistance for equipment design for producing medical devices and components.
  • Responsible for processing ECO's.
  • Supports production and manufacturing.
  • Analyzes and documents test results for development and pilot production runs.
  • Responsible for tooling maintenance and upgrades.
  • Responsible for manufacturing methods and their transfer into production.
  • Engineering support which includes; vendor contact and auditing specification.
  • Develops and tests components and assemblies of manufacturer's products.
  • Assists in special projects as needed. 
  • Contributes to team effort by accomplishing related duties as requested.

Required Knowledge, Skills and Abilities: 

  • Demonstrated analytical and problem solving skills. 
  • Experience in new product development, introduction processes and procurement protocols. 
  • Effective communication skills both verbal and written. 
  • Ability to function as part of a team, and accomplish assigned tasks independently. 
  • The ability to be flexible while maintaining a positive attitude.

Minimum Requirements:

  • Bachelors or Masters' Degree in Engineering, or equivalent. 
  • A minimum of five years related manufacturing experience. 
  • Good computer skills, including MS Office applications (Word/Excel) are required.

Quality Requirements 

  • Build Quality into all aspects of their work by maintaining compliance to all quality requirements.
  • Ensure compliance to all FDA and Worldwide Quality & Compliance regulations (As applicable to the job function).
  • Must have the education and experience to understand and comply with U.S. and Worldwide medical device regulations (As applicable to your job function).
  • Attend all required Quality & Compliance training at the specified interval.
  • Adopt the “Beyond Compliance Quality Culture” in the work environment; always meet and exceed requirements.

Environmental/Safety/Physical Work Conditions: 

  • Ensures environmental consciousness and safe practices are exhibited in decisions.
  • Duties are performed in an office/manufacturing environment.  Personal protective equipment may be required as dictated by work environment.


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