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| Job #03609 |
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| About our client |
| Our client was founded over 100 years ago. 1874. For the past 40 years, our client has stood out as the market leader in providing solutions in soft tissue reconstruction solutions including products for hernia repair, specialized surgical procedures, fixation and biologic implants. The company continues to maintain its leadership position in the medical device industry with an expanded portfolio of proven, innovative solutions. |
| Position |
Location |
| Senior Regulatory Affairs Associate |
Rhode Island |
| Salary |
| Highly competitive package, commensurate with experience |
| Responsibilities |
| 1) Contribute to PMA and 510k submissions to the FDA |
| Requirements |
| 1) 5 – 8 years of experience in directly submitting 510k and PMAs for Class II and Class III medical devices |

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