Senior Regulatory Affairs Specialist - Medical Devices (Hybrid)
$89.2k - $169.5kBoston Scientific - Minnetonka
Boston Scientific is seeking a Senior Regulatory Affairs Specialist to join our team in Irvine, CA. The role involves supporting regulatory compliance and submissions for our active implantable device portfolio. Candidates should have a Bachelor's Degree in a scientific field and at least 4 years of experience in Regulatory Affairs, particularly with 510(k) submissions. The position requires strong analytical skills and effective communication. This hybrid role offers competitive compensation ranging from $89,200 to $169,500 depending on experience. #J-18808-Ljbffr Boston Scientific
- ...Position : Senior Regulatory Affairs Specialist Location : Irvine, CA Duration : 10 Months Total... ...week : 40.00 1st Shift Client : Medical Devices Company Job Category : Clinical... ...or GC EAD or OPT or EAD or CPT Hybrid onsite 3 days JOB DESCRIPTION...SeniorMedical deviceContract workDay shift
- ...Senior Regulatory Affairs Specialist At Boston Scientific, we'll give you the opportunity... ...Specialist position (hybrid work mode) supporting our... ...growing active implantable device portfolio. This role will... ...Affairs experience in the medical industry Prior experience...SeniorMedical deviceWork at officeLocal area3 days per week
$70 - $85 per hour
A leading medical device company based in South Orange County is seeking a Senior EMC Engineer for product certification and wireless electrical engineering. This hybrid role requires 4 days onsite per week. Ideal candidates will have a BS degree with at least 4 years of...SeniorMedical device$92k - $148.35k
...Job Function: Regulatory Affairs Group Job Sub... ...best talent for a Senior Regulatory Affairs Specialist . This role will work a Hybrid/Flex schedule with 3... ...function such as Quality, Medical, Clinical, R&D. Demonstrated... ...Class III Medical Devices strongly preferred....SeniorMedical deviceContract workTemporary workLocal areaImmediate startFlexible hours3 days per week$92k - $148.35k
Senior Regulatory Affairs Specialist Location: Irvine, California or Milpitas, California (Hybrid/Flex schedule, 3 days on-site). Purpose The Senior... ...equivalent field such as Quality, Medical, Clinical, or R&D.... ...Class II or Class III Medical Devices strongly preferred....SeniorMedical deviceContract workTemporary workLocal areaFlexible hours- ...in California is urgently hiring a Regulatory Affairs Specialist. This role involves planning and implementing... ...regulatory submissions for medical devices and requires in-depth knowledge of healthcare... ...ability to work independently in a hybrid work environment. Responsibilities...Medical deviceImmediate start
- A leading global medical device company is seeking a Sr. Clinical Research Specialist based in Irvine, CA. This full-time position emphasizes supporting clinical trial... ...with external site personnel. The role offers a hybrid work model with comprehensive benefits including...SeniorMedical deviceFull time
$125k - $130k
...collaborating with physicians and institutions to develop elegant medical devices. Our products are being used by physicians across the... ..., come and join us! About this opportunity - Senior Regulatory Affairs Specialist Description: The Senior Regulatory Affairs...SeniorMedical deviceWork at office- A leading medical devices company is seeking a Regulatory Affairs Specialist to join their team based in Irvine, CA. The candidate will be responsible for planning and implementing regulatory submissions while ensuring compliance with healthcare regulations. They will...Medical device
$92k - $148.35k
Johnson & Johnson is seeking a Senior Regulatory Affairs Specialist to provide regulatory support for product lifecycle activities based in Irvine, California... ...to $148,350, alongside comprehensive benefits including medical, dental, and 401(k) plans. #J-18808-Ljbffr Johnson &...SeniorMedical device$50 - $55 per hour
A leading consulting firm based in Irvine, CA is seeking a Senior Project/Program Manager for a 12+ month contract. The role involves managing large-scale projects in the medical technology sector, requiring skills in new product development and project management. Ideal...SeniorMedical deviceContract work- ...Regulatory Affairs Representative Responsibilities: Represent Regulatory Affairs on cross-functional project teams and provide strategic... ...lifecycle planning and regulatory requirements for non-medical devices, and medical devices. Assess the acceptability of...SeniorMedical device
- ...Responsibilities: Represent Regulatory Affairs on cross-functional project teams and provide strategic input and technical guidance... ...lifecycle planning and regulatory requirements for non-medical devices, and medical devices. Assess the acceptability of documentation...SeniorMedical device
$92k - $130k
...Regulatory Affairs Specialist Make a meaningful difference to patients around the world. From design to production, our Regulatory Affairs... ...knowledge and understanding of global regulations relevant to medical devices, Class II and/or Class III devices Full knowledge and...SeniorMedical device- A leading medical device firm seeks an Electrical Engineer for their Irvine, CA location. The role involves gap analysis in compliance, project... .... The position offers an on-site schedule with a potential hybrid option after the candidate is established in the team. #J-1880...Medical device
- ...to support manufacturing projects. Candidates should have at least 5 years of engineering experience and proficiency in Mechanical CAD tools. The position offers a hybrid work environment with a focus on collaboration and innovation. #J-18808-Ljbffr MillenniumSoft IncMedical device
- A leading medical device organization seeks a Senior Software Engineer to modify and manage Android OS for compliance with medical device... ..., implementing OS-level changes, and ensuring regulatory compliance. This is a hybrid position in California and offers the...SeniorMedical deviceContract work
- ...Job Description Our F500 Medical Device client has an exciting opportunity for a Senior Software Engineer. Job... ...maintaining software traceability and regulatory documentation. • Adapt and... ...extension • Work Set-Up: Hybrid in Arbor Lakes, MN • Start Date...SeniorMedical deviceContract workTemporary work
$81k - $116k
...as needed and escape as appropriate. Evaluate complaints for Medical Device Reporting (MDR). Prepare and submit MDR reports to FDA. Process... ..., and evaluation of events for reportability to applicable regulatory bodies. How you will make an impact: Assess complaint information...SeniorMedical deviceWork experience placementRemote work- Electrical Engineer — Medical Device (Onsite/Hybrid — Irvine, CA) Contract Irvine, United States | Posted on 04/16/2026 From development to commercialization... ...partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our...Medical deviceContract work
- BD Mexico is seeking a Senior Manager of Embedded Software Engineering... ...software development for medical devices. You'll manage and develop teams, ensure regulatory compliance, and collaborate with... ...standards. The position includes a hybrid work model with a minimum in-office...SeniorMedical deviceWork at office
- Cannon Corp is seeking a Civil Senior Principal Engineer Land Development in Irvine, California. This role involves managing civil engineering... ...satisfaction. The position offers a competitive salary and a hybrid work schedule. #J-18808-Ljbffr American Meteorological SocietySenior
$126.6k - $210.9k
...Senior Staff Regulatory Affairs Specialist Irvine, California As a Senior Staff Regulatory Affairs Specialist... ...access. Work Flexibility: Hybrid or Onsite Hybrid candidates must... ...Annual Health benefits include: Medical and prescription drug insurance, dental...SeniorTemporary workLocal areaFlexible hours$85 - $92 per hour
...Religion/LGBTQI/Age/Veterans.” Job Title: Senior Software Engineer (C/C++) Job Category: Information Technology Industry: Medical Device Industry Job Location: Irvine, CA Zip Code... ...extension Client Domain: Medical device Industry Hybrid schedule: Onsite 4 days 1 day remote....SeniorMedical deviceContract workRemote workShift work- ...Shift** : Mon - Fri, 8:30am - 5pm + **Hybrid** : In-office 2x/week + Overtime based... ...business needs **What you will do** As a Senior Customer Service Representative, you... ...+ Adheres to all applicable medical device mandated compliance requirements **What...SeniorMedical deviceHourly payMinimum wageTemporary workWork experience placementWork at officeLocal areaFlexible hoursDay shift
- ...Job Title: Global Regulatory Affairs Principal Specialist Location: Fort Worth, TX, Johns Creek, GA, or Lake Forest, CA Summary of Position... ...Ensuring rapid and timely approval of new medical devices and continued approved status of marketed medical devices...Medical deviceVisa sponsorshipRelocation package
- A leading medical device company is seeking a Clinical Budgets Analyst in Irvine, CA, to negotiate and manage budgets for clinical trials.... ...related to the healthcare industry. This role offers competitive pay and a hybrid work model. #J-18808-Ljbffr Edwards LifesciencesMedical device
- ...Senior Design Assurance Engineer At Boston Scientific, we'll... ...and compliant with BSC and regulatory requirements. This Design Quality... .... This role follows a hybrid work model requiring employees... ...product development or related medical device / regulated industry...SeniorMedical deviceWork at officeLocal areaRemote workRelocation package3 days per week
$102.7k - $171.1k
Stryker Corporation is seeking a Product Manager in Irvine, CA to lead product development from concept through launch. This hybrid position requires onsite presence at least four days a week for collaboration with cross-functional teams. Candidates must have a Bachelor...Medical device$124.7k - $205.8k
A global medical technology company is seeking a Principal Electrical Engineer in Irvine, CA. This role involves supporting the development of electronic hardware for medical device systems. Candidates should have a strong background in electrical engineering, particularly...SeniorMedical device
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