ConforMIS, Inc. Burlington, MA
Project Documentation Engineer
To apply go to. http://www.conformis.com/About-Us/Careers
Job Description:
The Project Documentation Engineer is responsible for the documentation of product design and improvements, project completion plans as well the creation of documentation in the support of quality systems.
Essential Duties and Responsibilities:
- Create documentation for QSR compliance in support of engineering projects
- Write document change orders
- Communicate with production design, marketing, manufacturing and suppliers to gain knowledge into product design requirements
- Develop design documentation for the manufacture of product including drawings, product specifications and product validations, work instructions for CAD production
Qualification:
- BS in Mechanical Engineering or equivalent degree
- Minimum of 2 years experience in the engineering of medical devices
- Experience with documentation associated with medical device design and manufacturing
- A minimum of 2 years experience in computer engineering applications
- Knowledge of CAD/CAM software such as ProEngineer or Solidworks
Knowledge/Skills/Abilities:
- MS Office skills, a high proficiency in MS word a must
- Excellent written and verbal communication skills
- Excellent research, problem-solving and learning skills
- Must be able to work in a team environment, execute responsibilities with minimal direct supervision, and have a high attention to detail
- Busy work environment with frequent interruptions
- Must be aware of hazards within the company; adhere to quality and safety standards established by FDA and other regulatory agencies
- Able to work in changing environments (reduced lighting, increased noise, temperature variances, unpleasant odors, etc.)
ConforMIS is an Equal Opportunity Employer
Job posted - 1/31
Job Description:
The Project Documentation Engineer is responsible for the documentation of product design and improvements, project completion plans as well the creation of documentation in the support of quality systems.
Essential Duties and Responsibilities:
- Create documentation for QSR compliance in support of engineering projects
- Write document change orders
- Communicate with production design, marketing, manufacturing and suppliers to gain knowledge into product design requirements
- Develop design documentation for the manufacture of product including drawings, product specifications and product validations, work instructions for CAD production
Qualification:
- BS in Mechanical Engineering or equivalent degree
- Minimum of 2 years experience in the engineering of medical devices
- Experience with documentation associated with medical device design and manufacturing
- A minimum of 2 years experience in computer engineering applications
- Knowledge of CAD/CAM software such as ProEngineer or Solidworks
Knowledge/Skills/Abilities:
- MS Office skills, a high proficiency in MS word a must
- Excellent written and verbal communication skills
- Excellent research, problem-solving and learning skills
- Must be able to work in a team environment, execute responsibilities with minimal direct supervision, and have a high attention to detail
- Busy work environment with frequent interruptions
- Must be aware of hazards within the company; adhere to quality and safety standards established by FDA and other regulatory agencies
- Able to work in changing environments (reduced lighting, increased noise, temperature variances, unpleasant odors, etc.)
ConforMIS is an Equal Opportunity Employer
Job posted - 1/31
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