- Dentsply Sirona (Sarasota, FL)
- …Experience:** + 5(+) years of experience in regulatory affairs, preferably in the medical device industry + Experience with leading regulatory submissions and ... and oral health products as well as other consumable medical devices under a strong portfolio of world class...the Sarasota, FL location.** **Job Summary:** **The Senior Regulatory Specialist is a contributing member of cross-functional teams in… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …EU technical documentation under MDR, and other global regulatory filings. + Evaluate medical device regulations and lead the development of global regulatory ... collaboration and influencing skills. + Current knowledge of US and European medical device regulations. + Strong technical writing skills and ability… more
- Medtronic (Los Angeles, CA)
- …**Must Have: Minimum Requirements** + Bachelor's degree + Minimum of 7 years of medical device sales experience + Field-based role that requires 50% travel ... **A Day in the Life** The Executive Stapling Robotics Specialist is a key technical and strategic expert responsible...objectives + Proven track record in sales within the medical device or healthcare industry, preferably in… more
- embecta (Parsippany, NJ)
- …(eg engineering, bioengineering, biology, chemistry). + 5+ years Regulatory Affairs experience in medical device companies. + Must have current knowledge of the ... US and European Medical Device regulations. + Demonstrated success in the preparation and completion of 510(k) and EU MDR regulatory submissions to FDA and EU… more
- BD (Becton, Dickinson and Company) (Salt Lake City, UT)
- …ensure US, EU, and other global regulatory requirements are met + Evaluates medical device regulations and leads development of global regulatory strategies to ... degree or higher + 6-8 years' Regulatory Affairs experience in the medical device industry + Experience leading communications with FDA, EU notified bodies, and… more
- Otsuka America Pharmaceutical Inc. (Jackson, MS)
- …**Experience & Qualifications** + A minimum of 2 years of pharmaceutical or medical device sales experience. + Must reside within a commutable distance ... with a focus on pharmaceutical products to meet unmet medical needs and nutraceutical products for the maintenance of...In Otsuka's evolved customer engagement model, a Neuroscience LTC Specialist will engage HCPs through a variety of in-person,… more
- Abbott (Arecibo, PR)
- …colleagues serve people in more than 160 countries. **Job Description** **Technical Service Specialist ** **, this position is for the medical devices, Cardiac ... spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000… more
- State of Colorado (Colorado Springs, CO)
- …Scale/Hybrid Inspector (Compliance Specialist II) Print (https://www.governmentjobs.com/careers/colorado/jobs/newprint/5142294) Apply CDA-Large Scale/Hybrid ... Inspector (Compliance Specialist II) Salary $50,856.00 - $61,032.00 Annually Location Colorado Springs, CO Job Type Full Time Job Number BAA-00662-11132025… more
- GRAIL (Durham, NC)
- …metrics) as part of Measurement, Analysis, and Improvement activities, rolling up into medical device QMR and clinical laboratory QMI meetings. + Facilitate ... technical area.8+ years of related experience (Masters 5+ years) working within a medical device , pharmaceutical, or biotech QMS, with expertise in CAPA, NCR,… more
- Integra LifeSciences (Plainsboro, NJ)
- …US. Food and Drug Administration Regulations, ISO 9001, ISO 13485:2016 Standard, European Medical Device Directives, Canadian Medical Device Regulations, ... patient outcomes and set new standards of care. The **Quality Compliance Specialist ** will provide quality compliance support to the Collagen Manufacturing Center… more