We offer our employees a comprehensive, competitive program of benefits and a corporate culture based on core values of making a difference in lives of people, excellence and integrity.
Position: Regulatory Affairs Specialist
Description: Provides regulatory guidance and expertise to global project team on the assigned project(s) of responsibility. Identifies regulatory requirements and data reporting deadlines to ensure registration and approval of drug products
Requirements: MS in Science Field and 10+ years of experience in device and drug approval process. Excellent knowledge of ISO 13485, EMEA, EU and FDA regulations.
Position: Quality Assurance Engineer
Description: Leads the Quality Assurance objectives in accordance with company's global corporate policy and goals. Assists in preparation of regulatory documents.
Requirements: MS in Science Field and 5+ Years of Experience. Thorough understanding of ISO 13485, EMEA, EU and FDA regulations.