Job Description Summary As Senior Regulatory Affairs Specialist, you will will primarily focus on maintaining continued market access within our existing product portfolio and provide regulatory support for new product development projects. Job Description We are the makers of possible BD
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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
DemeTECH is seeking a highly motivated and detail-oriented Sr. Regulatory Affairs Specialist to join our team. The ideal candidate will play a pivotal role in ensuring our products meet all regulatory standards and achieve timely market access. This role involves
JOB SUMMARY The Regulatory Affairs Associate is required to work on a wide variety of regulatory tasks in maintenance of technical documentation, CE marking new devices and maintaining technical files to meet relevant regulatory requirements. ESSENTIAL JOB DUTIES & RESPONSIBILITIES
We are seeking a Senior Regulatory Affairs Specialist for a very important client. Duties: 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, product registration submission,
We are seeking a Senior Regulatory Affairs Specialist for a very important client. Role Overview: Perform assigned regulatory activities including submissions/responses to country authorities. Daily Responsibilities • Plan and prepare documents for EU MDR Technical File original submissions or responses to
(Must be able to re-locate to Naples, Florida; generous relocation package offered) Do you want to work for a global medical devices organization that is intended to provide full ongoing compliance and new submissions to support
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 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 · 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 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
Position: Product Regulatory Specialist II / Snr Regulatory Specialist Location: Rosemont, IL - Hybrid 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. Interfaces with