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Work with internal and external resources to design and develop new medical devices.
Design, develop and coordinate design verification and validation activities.
Perform verification activities including writing protocols and reports.
Create and document intellectual property according to established company procedures.
Work with cross-functional team to complete product development deliverables for new product launches.
Present recommendations/novel concepts to the team.
Maintain appropriate records for all test equipment and update Device History Records.
Bachelors Degree in Mechanical, Materials Science, Biomedical Engineering, or related discipline.
A minimum of 3 years of engineering experience in product and process development. Preferred medical device product and/or process development experience.
Strong analytical skills and problem solving skills.
Ability to communicate well through written and verbal means.
Ability to travel - international travel may be required in order to gain clinical knowledge, work with customers, interact with vendors, launch products, etc.
Additional Preferred Qualifications:
Experience in medical device manufacturing and/or design.
Knowledge of design control and design verification activities.
Ability to interface effectively with health care professionals and medical device customers.
Working knowledge of solid modeling (Solid Works preferred).
Working knowledge of business applications such as Microsoft Office (Word, Excel, PowerPoint, etc.).
To apply for this position, please visit
BioTech FYI Center