Job Summary

A scientific staffing company needs applicants for an opening for a Telecommute Pharmaceutical Post Market Surveillance Specialist.

Core Responsibilities of this position include:

• Translating case notes, reviewing, managing and closing complaints records in the complaint handling system
• Evaluating post-market data and updating risk management documentation
• Conducting post-market surveillance activities to analyze post-market quality issues and trends

Qualifications Include:

• BS/MS degree in Engineering or related
• 3 years of experience in medical device quality functions
• Knowledge of FDA's 21 CFR 820, 21 CFR 803, ISO 13485:2016, ISO 14971, MDD, EU MDR, MDSAP