- Stryker (Portage, MI)
- …Master's in Regulatory Affairs). + General understanding of FDA, EU, and international medical device regulations. Health benefits include: Medical and ... We are seeking a **Staff Regulatory Affairs Specialist ** to join our Medical Division...ensuring compliance with evolving regulatory requirements. You will assess device changes, monitor emerging regulatory intelligence, and lead regulatory… more
- Abbott (Chicago, IL)
- …relevant technical field, engineering) or equivalent/related experience. + 7+ years clinical medical device experience or equivalent, ideally with CRM products. ... and present effectively written and verbal communications. + Thorough familiarity with medical device industry policies, operations and procedures. + Expert… more
- Globus Medical, Inc. (Audubon, PA)
- …combined with at least 2-3 years of healthcare compliance experience with a medical device or pharmaceutical company. + Compliance and Ethics Professional ... their lives as quickly as possible. **Position Summary** **:** The Compliance Specialist contributes to strengthening the Globus Medical Compliance Program by… more
- CalSTRS (Sacramento, CA)
- Job Posting: CalSTRS Benefits Specialist State Teachers' Retirement System JC-499854 - CalSTRS Benefits Specialist ASSOCIATE GOVERNMENTAL PROGRAM ANALYST ... MSC manager (Pension Program Manager II), the CalSTRS Benefits Specialist independently performs a wide variety of the more...+ Flexible work hours + Remote work options + Medical benefits, including health, dental and vision insurance +… more
- IQVIA (Fort Worth, TX)
- …is a fast-growing business focused on delivering fit for purpose **solutions to the medical device and in vitro diagnostics industry.** We are looking for a ... sales initiatives. **Job Overview** . As a Solution Sales Specialist , you will engage with our **MedTech** customers to...+ Possesses knowledge of key marketplace issues for the ** Medical Device / MedTech industry** and related… more
- Danaher Corporation (Richmond, IL)
- …field or equivalent experience. + Minimum of two years' experience within medical device /IVD, across a variety of regulatory submissions, compliance initiatives, ... actions. + Experience with ISO 13485:2016, IVD/MDR Regulations, FDA GMP and domestic/international Medical Device Regulations. It would be a plus if you also… more
- Globus Medical, Inc. (Audubon, PA)
- …or higher with minimum of 2 years progressive work experience, preferably in the medical device industry or other regulated industry. * Ability to review ... At Globus Medical , we move with a sense of urgency...lives as quickly as possible. **Position Summary:** The Documentation Specialist will be responsible for the functions of In-bound… more
- Actalent (Santa Clara, CA)
- …requires a strong understanding of complaint handling processes within the medical device or pharmaceutical industry. Responsibilities + Conduct investigations ... Job Title: Quality Complaint Specialist Job Description We are seeking a dedicated...Manufacturing, and Regulatory. + Determine regulatory reportability and submit Medical Device Reports (MDRs) to the appropriate… more
- Edwards Lifesciences (Austin, TX)
- …Degree or equivalent in Nursing or related field, 5 years experience related to medical device , Cathlab, and/or clinical experience in an acute care environment ... and be part of our inspiring journey. The Clinical Specialist at IHFM plays a vital support role, reporting...it relates to the business + Moderate understanding of medical device regulatory requirements and documents, … more
- Bausch + Lomb (San Diego, CA)
- …etc. **Responsibilities** + In-service (train) customer ophthalmic staff on company-manufactured medical device equipment, according to company standards, to ... and calculation software. + Certify customer ophthalmic staff on company-manufactured medical device equipment after training during surgery observation &… more