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Public affairs specialist • san jose ca

Last updated: 2 days ago
  • Promoted
Senior Regulatory Affairs Specialist

Senior Regulatory Affairs Specialist

IntuitiveSunnyvale, California, USA
Full-time
Regulatory Affairs serve as the primary regulatory representative on product and project teams supporting product lifecycle management activities. Responsibilities include developing regulatory plan...Show moreLast updated: 19 days ago
  • Promoted
Senior Regulatory Affairs Specialist

Senior Regulatory Affairs Specialist

SI-BONESanta Clara, CA, US
Full-time
Senior Regulatory Affairs Specialist.SI-BONE is a fast-growing, publicly traded medical device company that is an industry pioneer in minimally invasive sacropelvic solutions.Our mission is to help...Show moreLast updated: 30+ days ago
  • Promoted
Senior Regulatory Affairs Labeling Specialist

Senior Regulatory Affairs Labeling Specialist

PROCEPT BioRoboticsSan Jose, CA, US
Permanent
Senior Regulatory Affairs Labeling Specialist.Embark on an enriching journey with PROCEPT BioRobotics, where our vision, mission, and values guide everything we do as a company.At PROCEPT, we put t...Show moreLast updated: 30+ days ago
  • Promoted
Government Affairs Director

Government Affairs Director

Rush Street InteractiveSan Jose, CA, US
Full-time
Rush Street Interactive (NYSE : RSI) is a market leader in online casino and sports betting, currently operating real-money gaming with our brands : BetRivers. We're building bridges between online, s...Show moreLast updated: 25 days ago
Regulatory Affairs Specialist - Contractor

Regulatory Affairs Specialist - Contractor

Align TechnologySan Jose, California
Full-time
The Regulatory Affairs Specialist- Contractor will assist or lead a variety of regulatory tasks in support of global regulatory strategy, regulatory assessment for modified product, regulatory fili...Show moreLast updated: 30+ days ago
  • Promoted
AI Sales Specialist, ISV, Google Public Sector

AI Sales Specialist, ISV, Google Public Sector

California StaffingSunnyvale, CA, US
Full-time
AI Sales Specialist, ISV, Google Public Sector.Experience owning outcomes and decision making, solving ambiguous problems and influencing stakeholders. deep expertise in domain.Minimum qualificatio...Show moreLast updated: 2 days ago
  • Promoted
Regulatory Affairs Manager

Regulatory Affairs Manager

Gandiva InsightsSan Jose, California, USA
Full-time
Title : Regulatory Affairs Manager.The Manager supports Global Reg Teams in the development and execution of global nonclinical / clinical regulatory strategies through a programs lifecycle.The Mana...Show moreLast updated: 16 days ago
  • Promoted
Regulatory Affairs Associate

Regulatory Affairs Associate

KyybaSanta Clara, CA, US
Full-time
AN HOUR W2 CONTRACT 6 MONTHS+ Responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approva...Show moreLast updated: 30+ days ago
  • Promoted
Senior Regulatory Affairs Specialist - Vision

Senior Regulatory Affairs Specialist - Vision

J&J Family of CompaniesMilpitas, CA, US
Full-time
Senior Regulatory Affairs Specialist.Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments...Show moreLast updated: 11 days ago
Public Relations Specialist

Public Relations Specialist

VirtualVocationsSanta Clara, California, United States
Full-time
A company is looking for a Public Relations Specialist.Key Responsibilities : Proactively identify news angles and collaborate with PR agency partners to secure media coverage Draft and edit pres...Show moreLast updated: 30+ days ago
Clinical Affairs Training Specialist

Clinical Affairs Training Specialist

RXSIGHT INCSan Jose, CA, US
Full-time
RxSight® is an ophthalmic medical technology corporation headquartered in Aliso Viejo, California that has commercialized the world’s first and only adjustable intraocular lens (IOL) that...Show moreLast updated: 30+ days ago
  • Promoted
ntern Public Affairs, Digital Strategy and Governance

ntern Public Affairs, Digital Strategy and Governance

GileadSan Jose, CA, US
Full-time
At Gilead, we're creating a healthier world for all people.For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer working relentlessly to develop therapie...Show moreLast updated: 17 days ago
  • Promoted
Clinical Affairs Training Specialist

Clinical Affairs Training Specialist

RxSight, Inc.San Jose, CA, United States
Full-time
RxSight® is an ophthalmic medical technology corporation headquartered in Aliso Viejo, California that has commercialized the world's first and only adjustable intraocular lens (IOL) that is custom...Show moreLast updated: 30+ days ago
Public Benefit Specialist

Public Benefit Specialist

Ensemble Health PartnersRegional Medical Center, Firelands
Full-time
Thank you for considering a career at Ensemble Health Partners!.Ensemble Health Partners is a leading provider of technology-enabled revenue cycle management solutions for health systems, including...Show moreLast updated: 30+ days ago
Regulatory Affairs Specialist - Ion

Regulatory Affairs Specialist - Ion

Intuitive SurgicalSunnyvale, CA, United States
Full-time
At Intuitive, we are united behind our mission : we believe that minimally invasive care is life-enhancing care.Through ingenuity and intelligent technology, we expand the potential of physicians to...Show moreLast updated: 30+ days ago
  • Promoted
Regulatory Affairs Principal

Regulatory Affairs Principal

DanaherSunnyvale, California, USA
Full-time
Are you ready to accelerate your potential and make a real difference within life sciences diagnostics and biotechnology. Danahers 15 operating companies our work saves livesand were all united by a...Show moreLast updated: 12 days ago
  • Promoted
Regulatory Affairs Manager

Regulatory Affairs Manager

Katalyst Healthcares & Life SciencesSan Jose, CA, US
Full-time
Responsibilities : Regulatory submissions including original ANDAs, amendments, annual reports, supplements and PADERs to company applications. Preparation / review of original submission / amendments / su...Show moreLast updated: 30+ days ago
  • Promoted
Sr. Regulatory Affairs Specialist

Sr. Regulatory Affairs Specialist

Becton DickinsonMilpitas, CA, US
Full-time
Senior Regulatory Affairs Specialist.BD Life Sciences is recruiting for a Senior Regulatory Affairs Specialist in San Milpitas, CA. Regulatory Affairs Specialist will be responsible for the preparat...Show moreLast updated: 30+ days ago
  • Promoted
Sr. Regulatory Affairs Specialist

Sr. Regulatory Affairs Specialist

BDSan Jose, CA, US
Full-time
Be part of something bigger! BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics, and the deli...Show moreLast updated: 25 days ago
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Senior Regulatory Affairs Specialist

Senior Regulatory Affairs Specialist

IntuitiveSunnyvale, California, USA
19 days ago
Job type
  • Full-time
Job description

Primary Function of Position

The Sr. Regulatory Affairs serve as the primary regulatory representative on product and project teams supporting product lifecycle management activities. Responsibilities include developing regulatory plans reviewing design input / output documentation identification of applicable standards and guidance documents performing regulatory assessments to determine the impact of design / process changes preparing regulatory submissions maintaining regulatory filings and licenses and interacting with regulatory agencies

Essential Job Duties

  • Serve as the global regulatory liaison and primary point of contact for product and project teams.
  • Provide regulatory guidance to product teams develop regulatory plans and review and approve product design control documentation.
  • Determine regulatory pathways and formulate regulatory strategies for the U.S. and Canadian markets. Assess regulatory impact on design materials labeling packaging manufacturing processes and facility changes. Influence and lead global regulatory strategies.
  • Author and lead regulatory documentation and submissions including U.S. FDA 510(k) premarket notifications internal Letters to File pre-submissions with minimal supervision.
  • Coordinate with technical experts to provide additional data / information requested by regulatory agencies and prepare responses to facilitate regulatory approvals.
  • Provide risk-based guidance and regulatory input to projects and issues ensuring cross-functional alignment and resolution.
  • Collaborate with international counterparts to support global regulatory submissions approvals and implementation rollouts.

Qualifications :

Required Skills and Experience

  • Minimum 8 years of regulatory affairs experience working in a medical device company (can be in combination with a regulatory affairs master degree; e.g. Masters in Regulatory Science)
  • In-depth understanding of US Medical Device regulations and EU MDR especially as it related to Digital and SW related projects.
  • Regulatory working knowledge of product lifecycle management design controls risk management verification and validation and product labeling requirement
  • Ability to work in a fast-paced environment and handle multiple projects simultaneously
  • Strong verbal and written communication skills proven ability to translate technical documentation into effective internal documentation and regulatory submissions
  • Team player who seeks to help and learn from colleagues seeing the department success as their own
  • Strong interpersonal and negotiation / influencing skills while maintaining a high level of professionalism
  • Proactively seeks to develop and become well-versed within the regulatory landscape.
  • Required Education and Training

  • Minimum B.S. or higher in Biomedical Engineering Electrical Engineering Mechanical Engineering or Pharmacy preferred. Non-technical degrees with equivalent complex medical device experience are acceptable.
  • Preferred Skills and Experience

  • RAPS Regulatory Affairs Certification (RAC) is a plus.
  • Additional Information :

    Due to the nature of our business and the role please note that Intuitive and / or your customer(s) may require that you show current proof of vaccination against certain diseases including COVID-19.  Details can vary by role.

    Intuitive is an Equal Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees and prohibit discrimination and harassment of any type without regard to race sex pregnancy sexual orientation gender identity national origin color age religion protected veteran or disability status genetic information or any other status protected under federal state or local applicable laws.

    Mandatory Notices

    U.S. Export Controls Disclaimer :   In accordance with the U.S. Export Administration Regulations (15 CFR 743.13(b)) some roles at Intuitive Surgical may be subject to U.S. export controls for prospective employeeswho are nationals from countries currently on embargo or sanctions status.

    Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note : the governments licensing process can take 3 to 6 months) or (ii) implement a Technology Control Plan (TCP) (note : typically adds 2 weeks to the hiring process).

    For any Intuitive role subject to export controls final offers are contingent upon obtaining an approved export license and / or an executed TCP prior to the prospective employeesstart date which may or may not be flexible and within a timeframe that does not unreasonably impede the hiring need. If applicable candidates will be notified and instructed on any requirements for these purposes.

    We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws.

    Preference will be given to qualified candidates who do not reside or plan to reside in Alabama Arkansas Delaware Florida Indiana Iowa Louisiana Maryland Mississippi Missouri Oklahoma Pennsylvania South Carolina or Tennessee.

    We provide market-competitive compensation packages inclusive of base pay incentives benefits and equity. It would not be typical for someone to be hired at the top end of range for the role as actual pay will be determined based on several factors including experience skills and qualifications. The target compensation ranges are listed.

    Remote Work : No

    Employment Type : Full-time

    Key Skills

    Athletics,Corporate Banking,Dreamweaver,Facilities,IT Support

    Experience : years

    Vacancy : 1