Regulatory Affairs Specialist
R&D Partners - San Jose, California, United States, 95199
Work at R&D Partners
Overview
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Overview
Compile and maintain regulatory documentation databases or systems. Coordinate efforts associated with the preparation of regulatory documents or submissions. Analyze product complaints and make recommendations regarding their reportability. Develop or conduct employee regulatory training. Communicate with regulatory agencies regarding pre-submission strategies, potential regulatory pathways, compliance test requirements, or clarification and follow-up of submissions under review. What we are looking for in a Regulatory Affairs Specialist II:
3-5 years of work experience Knowledge of US, EU, and Canada Medical Device Regulations Familiarity with PLM WindChill and Veeva RIM platforms (not a mandatory requirement) Why Choose R&D Partners?
As an employee, you have access to a comprehensive benefits package including: Medical insurance PPO, HMO & HSA 401k plan Employee Assistance Program Long-term disability Weekly payroll Online timecard approval Salary Range: $99,611 - $122,283 (Dependent on Experience) R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies. R&D Partners is an equal-opportunity employer.
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