- Caldera Medical (Westlake Village, CA)
- …Life for Women! Message from the Hiring Manager: In your role as a Sr. Regulatory specialist , you will develop and implement medical device regulatory ... Sr. Regulatory Affairs Specialist 100% ONSITE in...worldwide regulatory bodies. From developing and authoring regulatory submissions to providing critical input on… more
- Abbott (Alameda, CA)
- …life Sciences, Biology (or equivalent vocational qualifications) + Experienced in regulatory submissions for Pharmaceuticals, medical devices, and/or in vitro ... regulations or with EU and other international medical device regulations and submissions . + Familiar with relevant regulatory requirements for medical devices,… more
- Abbott (Santa Clara, CA)
- …clinical documentation for submission filing. + Compile, prepare, review and submit regulatory submissions to authorities. + Monitor impact of changing ... life Sciences, Biology (or equivalent vocational qualifications) + Experienced in regulatory submissions for Pharmaceutical, In vitro diagnostic devices and/or… more
- J&J Family of Companies (Santa Clara, CA)
- …Regulatory Agencies and Notified Body + Support publishing of worldwide regulatory submissions in compliance with geography-specific regulatory ... Description:** Johnson & Johnson is hiring for a **Associate Regulatory Operations Specialist - Shockwave Medica** l...requirements + Support verification and quality review of submissions and other responses to regulatory agencies… more
- Abbott (Alameda, CA)
- …presented to substantiate claims. You'll also have opportunities to participate in worldwide regulatory submissions . This is a broad scoped position with strong ... As an individual contributor in the function of a Regulatory Affairs Specialist you will provide support...product release. + Reviews protocols and reports to support regulatory submissions . + Supports all business segment… more
- Abbott (Santa Clara, CA)
- …clinical documentation for submission filing. + Compile, prepare, review and submit regulatory submissions to authorities. + Monitor impact of changing ... catheters and software, vessel closure devices and peripheral stents. This Senior Regulatory Affairs Specialist position is an onsite opportunity working out… more
- Abbott (Alameda, CA)
- ….. The individual has department level influence with experience in global regulatory submissions and on-market changes, and is generally recognized as ... life Sciences, Biology (or equivalent vocational qualifications) . Experienced in regulatory submissions for Pharmaceutical, in vitro diagnostic devices and/or… more
- Astrix Technology (Los Angeles, CA)
- …compensation package. **Responsibilities:** + Prepare & maintain necessary documentation for regulatory submissions , inspections and import activities. + Ensure ... ** Regulatory Affairs Specialist (Global)** Regulatory...to work independently + Demonstrated ability to prepare complex documents/ submissions and presentations INDBH We are an equal opportunity… more
- Kelly Services (Sunnyvale, CA)
- Kelly(R) Science & Clinical is seeking a Regulatory Affairs Process Specialist for a 6-month contract opportunity with a leading molecular diagnostics company ... progress in the biotechnology realm. **Workplace:** Remote US **Position Title:** Regulatory Affairs Process Specialist **Position Type:** 6-month contract **Pay… 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 ... guidance on device versus non-device functionality. + Prepare, submit, and manage regulatory submissions for SaMD products. + Evaluate the impact of changes to… more