Collabera is ranked amongst the top 10 Information Technology (IT) staffing firms in the U.S., with more than $550 million in sales revenue and a global presence that represents approximately 12,000+ professionals across North America (U.S., Canada), Asia Pacific (India, Philippines, Singapore, Malaysia) and the United Kingdom. We support our clients with a strong recruitment model and a sincere commitment to their success, which is why more than 75% of our clients rank us amongst their top three staffing suppliers.
Job Description
Associate MDR/Vigilance Specialists are responsible for the intake, documentation, Medical Device Reporting, and investigation of complaints for legacy Neuromodulation products in accordance with applicable internal procedures (work instructions) and external requirements (regulations or guidance from any and all regulatory bodies).
Position Responsibilities:
- Receive and assess product comments to determine need for complaint handling record.
- Document required information in Global Complaint Handling (GCH).
- Assess complaint file for missing required information. If information is missing, initiate attempts to gather information. Steps may include contacting outside parties.
- Communicate with outside parties in a professional and customer-focused manner that is in following with our Mission and enhances the Medtronic brand.
Qualifications
• 0-2 years experience in healthcare or medical device/pharmaceutical industry in safety or clinical data evaluation.
Additional Information
To know more and apply feel free to contact:
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