Regulatory Affairs Specialist
$50 - $54 per hourSunrise Systems
Our client, a leading Medical Device manufacturing company, is looking for a Regulatory Affairs Specialist. This is for an initial duration of 12 months and is located at Chaska, MN.
Job Title: Regulatory Affairs Specialist
Reference ID: 26-05136
Location: Chaska, MN
Duration: 12 months
Job Type: Contract (Candidates must be able to work on W2 without VISA sponsorship)
- The Senior Regulatory Affairs Specialist plans, coordinates, facilitates, and reports on Client regulatory programs.
- The incumbent's primary responsibilities will be the evaluation, coordination, preparation and implementation of post-market Regulatory Affairs activities.
- Responsibilities may include: - Administration of the company's complaint management program for compliance to corporate requirements
- Planning and implementing pre-market registration, reporting and compliance activities in accordance with the development center business plans.
- Implementing global regulatory compliance programs for product corrective action and/or adverse event reporting.
- Preparing premarket or other regulatory submissions (510(k), PMA, Technical Dossiers, etc.) for US and other governments.
- Additionally, may provide assistance to technical departments, manufacturing business centers and suppliers in the creation and structuring of clinical data for pre-market notifications.
- Functioning as a team expert for promotional materials review, experimental designs, data analysis and product labeling as they relate to registration and commercialization of medical devices.
- Educational requirements: Bachelor's degree in field with 5+ years exp. OR Master's degree in field with3+ years exp. Medical Technologist background and IVD experience strongly desired.
$47 - $52 per hour
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