- Search jobs
- San Jose, CA
- public affairs specialist
Public affairs specialist Jobs in San Jose, CA
Create a job alert for this search
Public affairs specialist • san jose ca
- Promoted
Senior Regulatory Affairs Specialist
IntuitiveSunnyvale, California, USA- Promoted
Senior Regulatory Affairs Specialist
SI-BONESanta Clara, CA, US- Promoted
Senior Regulatory Affairs Labeling Specialist
PROCEPT BioRoboticsSan Jose, CA, US- Promoted
Government Affairs Director
Rush Street InteractiveSan Jose, CA, USRegulatory Affairs Specialist - Contractor
Align TechnologySan Jose, California- Promoted
AI Sales Specialist, ISV, Google Public Sector
California StaffingSunnyvale, CA, US- Promoted
Regulatory Affairs Manager
Gandiva InsightsSan Jose, California, USA- Promoted
Regulatory Affairs Associate
KyybaSanta Clara, CA, US- Promoted
Senior Regulatory Affairs Specialist - Vision
J&J Family of CompaniesMilpitas, CA, USPublic Relations Specialist
VirtualVocationsSanta Clara, California, United StatesClinical Affairs Training Specialist
RXSIGHT INCSan Jose, CA, US- Promoted
ntern Public Affairs, Digital Strategy and Governance
GileadSan Jose, CA, US- Promoted
Clinical Affairs Training Specialist
RxSight, Inc.San Jose, CA, United StatesPublic Benefit Specialist
Ensemble Health PartnersRegional Medical Center, FirelandsRegulatory Affairs Specialist - Ion
Intuitive SurgicalSunnyvale, CA, United States- Promoted
Regulatory Affairs Principal
DanaherSunnyvale, California, USA- Promoted
Regulatory Affairs Manager
Katalyst Healthcares & Life SciencesSan Jose, CA, US- Promoted
Sr. Regulatory Affairs Specialist
Becton DickinsonMilpitas, CA, US- Promoted
Sr. Regulatory Affairs Specialist
BDSan Jose, CA, USThe average salary range is between $ 59,238 and $ 91,335 year , with the average salary hovering around $ 63,384 year .
- american sign language interpreter (from $ 70,941 to $ 551,925 year)
- investment banker (from $ 144,400 to $ 249,600 year)
- cardiothoracic surgeon (from $ 174,600 to $ 248,150 year)
- forensic pathologist (from $ 135,000 to $ 244,941 year)
- director of software engineering (from $ 183,000 to $ 240,000 year)
- psychiatrist (from $ 50,000 to $ 240,000 year)
- radiologist (from $ 57,103 to $ 238,613 year)
- chief investment officer (from $ 155,794 to $ 235,505 year)
- engineering director (from $ 151,059 to $ 235,000 year)
- product director (from $ 164,997 to $ 235,000 year)
- Milwaukee, WI (from $ 85,759 to $ 205,920 year)
- Detroit, MI (from $ 66,932 to $ 203,840 year)
- Richmond, VA (from $ 88,862 to $ 184,702 year)
- Pittsburgh, PA (from $ 92,202 to $ 179,085 year)
- Virginia Beach, VA (from $ 91,475 to $ 158,606 year)
- Springfield, MA (from $ 83,210 to $ 150,583 year)
- Springfield, IL (from $ 83,210 to $ 150,583 year)
- Columbia, MO (from $ 93,750 to $ 147,138 year)
- Washington, DC (from $ 87,495 to $ 145,145 year)
- Ann Arbor, MI (from $ 90,735 to $ 143,911 year)
The average salary range is between $ 63,384 and $ 130,070 year , with the average salary hovering around $ 85,830 year .
Related searches
Senior Regulatory Affairs Specialist
IntuitiveSunnyvale, California, USA- Full-time
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
Required Education and Training
Preferred Skills and Experience
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