Senior Regulatory Affairs Lead - Medical Devices
MillenniumSoft Inc
A reputable medical devices company is seeking a Senior Regulatory Affairs Coordinator for an onsite position in Irvine, CA. The role involves supporting US and EU regulatory submissions, developing regulatory strategies, and providing guidance on registration. Candidates should possess a Bachelor's degree in a scientific discipline and have 5-7 years of relevant experience. Strong skills in Microsoft Office, communication, and problem-solving are essential. Contract employment on W2 is required, with a commitment of 40 hours per week. #J-18808-Ljbffr MillenniumSoft Inc
$92k - $148.35k
Johnson & Johnson is seeking a Senior Regulatory Affairs Specialist to provide regulatory support for product lifecycle activities based in Irvine... ...00 to $148,350, alongside comprehensive benefits including medical, dental, and 401(k) plans. #J-18808-Ljbffr Johnson &...SeniorMedical device- A medical devices company is seeking a Regulatory Affairs Coordinator with 5-7 years of experience in the medical device industry. You will support regulatory submissions and collaborate on change notifications while ensuring compliance with global regulations. The ideal...SeniorMedical deviceFull timeContract workWork at officeDay shift
$145k - $205k
Edwards Lifesciences in Irvine, California, seeks a candidate to lead imaging-based patient screening efforts. The ideal applicant will have at least 8 years of experience in the medical device sector, with a strong background in advanced cardiovascular imaging and analytical...SeniorMedical device$137k - $235.75k
Johnson & Johnson in Irvine, California is looking for a Programming Leader in the Medical Devices Sector. This role entails leading a team of SAS and R programmers responsible for statistical deliverables for clinical trials. The ideal candidate will have over 8 years...SeniorMedical device- A leading technology company is seeking an NPD Program Manager to oversee the product development life cycle in Irvine, California... ...6 years' experience in managing complex NPD projects in the medical device industry, focusing on a mix of software, firmware, and hardware...SeniorMedical device
$92k - $130k
Edwards Lifesciences is looking for a Senior Labeling Specialist in California. This role involves collaborating cross-functionally to... ...on complex labeling projects, ensuring compliance with regulatory standards, and contributing to continuous process improvements....SeniorMedical device$145k - $205k
...Lifesciences Gruppe in Irvine, California, is seeking a functional lead for imaging-based patient screening. You will oversee... ...Engineering or Scientific field and 8 years of experience in the Medical Device industry. The role offers a competitive salary range of $145,0...SeniorMedical deviceRelocation$121.2k - $166.7k
A leading life sciences company in Irvine, California, seeks a Manufacturing Engineer III to lead the design and optimization of manufacturing... ...s or Master’s degree, with at least 7 years of experience in medical device manufacturing. Responsibilities include managing continuous...SeniorMedical device- ...Position : Senior Regulatory Affairs Specialist Location : Irvine, CA Duration : 10 Months Total Hours/week : 40.00 1st Shift Client : Medical Devices Company Job Category : Clinical Level of Experience : Mid-Level Employment Type : Contract on W...SeniorMedical deviceContract workDay shift
$89.2k - $169.5k
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...SeniorMedical device$170k - $200k
...field. For 45 years, Balt has been leading the way - collaborating with physicians... ...institutions to develop elegant medical devices. Our products are being used by... ...join us! About this opportunity - Senior Principal Regulatory Affairs Specialist Description The...SeniorMedical device- A medical devices company is seeking a Senior Regulatory Affairs Coordinator in Irvine, CA. The role involves supporting US and EU regulatory submissions, developing regulatory strategies, and providing guidance on registration requirements. Candidates should possess a...SeniorMedical deviceWork at office
- A leading medical devices firm seeks a Senior Regulatory Affairs Coordinator (Contract) in Irvine, CA. The role involves supporting US and EU regulatory submissions, developing regulatory strategies, and ensuring compliance with regulations. Candidates should have a Bachelor...SeniorMedical deviceFull timeContract workWork at office
- A leading medical devices company is seeking a Senior Regulatory Affairs Coordinator in Irvine, CA. The candidate will support regulatory submissions, develop strategies, and provide guidance to teams on product registrations. A Bachelor's degree in a scientific discipline...Medical deviceFull timeContract work
- ...Position : Senior Regulatory Affairs Coordinator Location : Irvine, CA Duration : 12 Months Total Hours/week : 40.00 1st Shift Client : Medical Devices Company Job Category : Clinical Level of Experience : Senior Level Employment Type : Contract on...SeniorMedical deviceContract workWork at officeDay shift
- ...Senior Regulatory Affairs Specialist At Boston Scientific, we'll give you the opportunity to harness... ...rapidly growing active implantable device portfolio. This role will be responsible... ...Regulatory Affairs experience in the medical industry Prior experience with 510(...SeniorMedical deviceWork at officeLocal area3 days per week
$92k - $130k
...Regulatory Affairs Specialist Make a meaningful difference to patients around the world. From design to production, our Regulatory... ...knowledge and understanding of global regulations relevant to medical devices, Class II and/or Class III devices Full knowledge and...SeniorMedical device- A dental product company in California is looking for a Regulatory Affairs Specialist. The role involves preparing and submitting product registrations to the FDA, maintaining compliance with regulations across the US, Canada, and EU, and conducting audits. Candidates...Senior
$83.9k - $120k
A leading dental products company located in California is seeking a Regulatory Affairs Specialist to prepare and submit product registrations, maintain company registrations, and analyze compliance metrics. The ideal candidate will have at least 5 years of experience in...Senior- A global pharmaceutical company seeks a Senior Manager of Regulatory Affairs to oversee advertising and promotional compliance and lead a team of regulatory professionals. The ideal candidate will have a Bachelor's degree in a relevant field and at least 7 years of industry...Senior
$126.6k - $210.9k
Stryker Corporation in Irvine, California is looking for a Senior Staff Regulatory Affairs Specialist to influence global regulatory strategy throughout the product lifecycle. You will collaborate closely with product development, quality, and clinical teams, and address...Senior- A medical device company is seeking a Senior Engineer, R&D to lead complex engineering projects for novel ophthalmic medical devices. You will design experiments, troubleshoot technical issues, and mentor junior engineers to achieve engineering milestones. The ideal candidate...SeniorMedical device
$121k - $171k
Edwards Lifesciences Belgium is seeking a Principal Engineer in Irvine, California to lead manufacturing equipment development for Transcatheter Heart Valves. This position involves designing complex electromechanical systems and collaborating with R&D to ensure manufacturability...SeniorMedical device- Lgm-Pharma, LLC in Irvine, CA is seeking a Senior Regulatory Affairs Specialist to manage the submission and approval processes for regulatory applications... ...interacting with regulatory agencies. The position offers medical, dental, vision benefits, and a company matching 401K plan....Senior
- A leading medical device company in Irvine, CA is looking for a talented marketing and strategy professional with a strong background in the healthcare industry. The role involves developing innovative commercial marketing strategies for the EVOQUE tricuspid valve system...SeniorMedical device
$92k - $148.35k
.... Job Function: Regulatory Affairs Group Job Sub Function... ...best talent for a Senior Regulatory Affairs... ...lifecycle stages. Leads preparation and submission... ...such as Quality, Medical, Clinical, R&D. Demonstrated... ...or Class III Medical Devices strongly preferred....SeniorMedical deviceContract workTemporary workLocal areaImmediate startFlexible hours3 days per week- A leading medical device organization seeks a Senior Software Engineer to modify and manage Android OS for compliance with medical device standards. The ideal... ...risks, implementing OS-level changes, and ensuring regulatory compliance. This is a hybrid position in California...SeniorMedical deviceContract work
$92k - $148.35k
Senior Regulatory Affairs Specialist Location: Irvine, California or Milpitas, California... ...product lifecycle stages. Leads preparation and submission... ...field such as Quality, Medical, Clinical, or R&D.... ...Class II or Class III Medical Devices strongly preferred. Experience...SeniorMedical deviceContract workTemporary workLocal areaFlexible hours- ...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
- ...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
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