div.content {background: #6c6f70}div.joqReqDescription {background: #FFF repeat-y; !important;font family: arial; !importanttext-align: left;color: #000;width: 900px !important;margin: 0 auto !important;position: relative;-webkit-column-count: 1;-moz-column-count: 1;padding-top: 489px;padding-left: inherit;padding-bottom: 50px;}div.joqReqDescription strong{ font family: arial;font-size: 14px;color: #000;}div.joqReqDescription p{ font family: arial;padding-left:0px;width: 892px;}div.joqReqDescription div.image-box {width:
Hi , Hope you are doing well. My name is Jagdeep and I am a resource professional with Kyyba Inc. I came across your resume in my database and wondered if you would be interested in
DePuy Synthes, Inc., part of the Johnson & Johnson MedTech companies, is currently recruiting for a Senior Regulatory Affairs Specialist to support Life Cycle Management and New Product Development. This role will work a Hybrid/Flex schedule with 3 days in
Hello, Hope you are doing great. This is Aleem from Intellectt INC; weve got an important role Senior Regulatory Affairs Specialist Temecula, CA 92591 with one of our prestigious clients. Interested candidates can please send your updated resume at aleem@intellectt.com
Hello Im Komal from Intellectt we have an opening for a Senior Regulatory Affairs Specialist in Temecula, CA. Please find the job details and description below and if interested You can reach me at komal@intellectt.com or call me at +1(732)-813-9025.
Role: Senior Regulatory Affairs Specialist Location: Temecula, CA - 92591 Duration: 08 Months Description: Years Experience: Must have 3-5 years of experiences in Medical Device Regulatory Affairs Skills: Have working knowledge in EU MDR Have working knowledge in Regulatory Change Assessment in Have
This position will be working with multiple business units to develop, update, and improve regulatory affair processes. Assist the strategy implementation and operations for regulatory affairs activities, including directing development of product registration submission, progress reports, supplements, amendments, or periodic
Role: Senior Regulatory Affairs Specialist Location: Temecula, CA - 92591 Duration: 08+ Months on W2 Shift Timings: 8 AM to 5 PM Skills Looking For: - Regulatory Submission Experience: Proficiency in US (FDA) and European (CE) regulatory submissions, particularly with Class 3
Abiomed, part of Johnson & Johnsons MedTech, is recruiting for a Senior Regulatory Affairs Specialist . Remote work options may be considered on a case-by-case basis and if approved by the Company Abiomed, part of Johnson & Johnson MedTech, is
Job Description Job Description Summary: The main function of a regulatory affairs specialist is to complete and maintain regulatory approvals and clearances of assigned products. Key Responsibilities: Create regulatory submissions (exercising judgment to protect proprietary information) for finalization and submission by
Job Description Job Description · Perform assigned regulatory activities including submissions/responses to country authorities. Daily Responsibilities - Job Description suppliers should use: · Plan and prepare documents for EU MDR Technical File original submissions or responses to
Job Description Job Description Position: Product Regulatory Specialist II / Snr Regulatory Specialist Location: Rosemont, IL Responsibilities: The Snr Product Regulatory Specialist is responsible for obtaining registrations and certification approvals for new and existing products, necessary to sell them to worldwide markets.
Job Description Job Description Must have 1-3 years of experiences in Medical Device Regulatory Affairs Skills: Have working knowledge in EU MDR Have working knowledge in Regulatory Change Assessment in Have working knowledge in US and EU medical device
Job Description Job Description Eastridge Workforce Solutions, in collaboration with a leading innovator in neurovascular device technology, is seeking an experienced Senior Regulatory Specialist to join the team. This individual will play a pivotal role in overseeing global product
Job Description Job Description SMS Staffing Inc is Hiring Immediately for a skilled Senior Regulatory Affairs Specialist . Job Title : Senior Regulatory Affairs Specialist Job Location: Temecula, CA, U.S.A. Job Type: Contract (possible extension) Pay: Starts at $31.00 an hour Shift Structure: 8:00
Job Description Job Description Salary: $100k + DOE OrthAlign, Inc., a Smart Technology, growing medical device company, has an immediate opening for a Senior Regulatory Affairs Specialist responsible for implementing regulatory strategies, assisting with the preparation, organization, and maintenance of documentation
Job Description Job Description Description: The Senior Regulatory Affairs Specialist will be responsible for ensuring compliance with all regulatory requirements for medical devices and pharmaceutical products. This position requires a deep understanding of the regulatory landscape and the ability to navigate complex
Biofourmis brings the right care to every person, no matter where they are. The company’s AI-driven solution collects and analyzes patient data in real time and identifies shifts that require proactive interventions. This vital innovation provides
Job Description Job Description Skills: Have working knowledge in EU MDR Have working knowledge in Regulatory Change Assessment in Have working knowledge in US and EU medical device submissions Have experience supporting internal and external inspections Work
Years Experience: Must have 3-5 years of experiences in Medical Device Regulatory Affairs Education: BA Degree Required Skills: Have working knowledge in EU MDR Have working knowledge in Regulatory Change Assessment in Have working knowledge in US and EU