About this role
Regulatory Affairs Spec at Drägerwerk AG & Co. KGaA. Location: Andover, Massachusetts, United States. Role: developing strategies, preparing submissions, maintaining compliance Requirements: BS in life sciences/engineering preferred; 3+ years regulatory medical device experience and 2+ years interacting with regulatory agencies; RAC a plus; knowledge of US and international device regulations; Microsoft application skills; strong communication. Category: Quality Assurance Seniority: Mid Level Tools: Microsoft Excel Certifications: rac Commitment: Full Time Workplace: Hybrid Languages: English