- Canon USA & Affiliates (Sacramento, CA)
- ** Regulatory Affairs Specialist - Post Market - req1434** **OVERVIEW** Reporting to the Director Regulatory Affairs , the Regulatory ... including MS Word, Excel, Oracle, Sales Force, etc. + 2 Years Regulatory Affairs experience in medical device industry required + Minimum Education Level: 2… more
- J&J Family of Companies (Santa Clara, CA)
- …United States of America **Job Description:** Johnson & Johnson is hiring for a **Sr Regulatory Affairs Specialist ** **- Shockwave** to join our team located ... the treatment of calcified plaque. **Position Overview** The Sr. Regulatory Affairs Specialist is an...guidelines, policies and regulations. + Experience with pre- and post -market medical device submissions such as 510(k), IDE, PMA,… more
- Abbott (Santa Clara, CA)
- …imaging catheters and software, vessel closure devices and peripheral stents. This Senior Regulatory Affairs Specialist position is an onsite opportunity ... in the Abbott Vascular Division. As an individual contributor, the function of a Senior Regulatory Affairs Specialist is to provide support for the … more
- Envista Holdings Corporation (Brea, CA)
- **Job Description:** The ** Regulatory Affairs Specialist ** creates, evaluates and completes regulatory tasks related to worldwide product registration ... + Bachelor's Degree (BA/BS) from four-year college/university + 2+ years of regulatory affairs experience in medical devices or other regulated industry,… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- **Job Description Summary** As Staff Specialist Regulatory Affairs , you will have a deep understanding of Risk Based frameworks, Agile SDLC, experience with ... a related field. + 3-5 years of practical experience regulatory affairs , with a focus on SaMD....with cloud-based, or multifunction software systems. + Familiarity with post -market surveillance requirements for SaMD. Salary ranges have been… more
- Abbott (Alameda, CA)
- …years' experience working with Class II, Class III medical devices and/or biologics/drugs. Regulatory Affairs Certification (RAC) is a plus. . Experience with ... corporate policies. . Oversee processes & improvements involved with Partnership regulatory activities . Ensure compliance with product post -marketing approval… more
- Abbott (Alameda, CA)
- …years' experience working with Class II, Class III medical devices and/or biologics/drugs. Regulatory Affairs Certification (RAC) is a plus. + Experience with ... glucose levels with our new sensing technology. **The Opportunity** The **Principal RA Specialist - US New Product Introduction** will work on-site out of our… more
- Veterans Affairs, Veterans Health Administration (Los Angeles, CA)
- Summary This Peer Specialist position may only be filled with a Veteran that meets statutory requirements that are detailed in the qualifications section. Locations: ... West LA Campus housing: 11301 Wilshire Blvd. 90073 Responsibilities The Peer Specialist functions as an interdisciplinary team member, assisting physicians and other… more
- AbbVie (San Francisco, CA)
- …based on qualifications listed below. Purpose: The Scientific/Medical Director, Medical Affairs provides specialist medical and scientific strategic and ... operational input into core medical affairs activities such as: health-care professional and provider interactions; generation of clinical and scientific data… more
- Meta (Burlingame, CA)
- **Summary:** We're seeking a regulatory affairs specialist to join our medical devices compliance team. You will get to work on wearables and Software as a ... wrist wearables, and other innovative devices. **Required Skills:** Medical Devices, Regulatory Specialist Responsibilities: 1. Interact directly with FDA and/or… more
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