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Regulatory Affairs Specialist Jobs in California

84 jobs

CyberCoders Search. Apply. Done. Learn more about CyberCoders Regulatory Affairs Specialist Apply Sunnyvale, CA Full-Time Unspecified Job Details Based in Sunnyvale, CA we are an established leader in the diagnostic industry! For over two decades, we have been helping medical professionals worldwide to make more accurate diagnoses to make therapy more effective. Currently, we are in need o...
CyberCoders Search. Apply. Done. Learn more about CyberCoders Sr. Regulatory Affairs Specialist Apply San Jose, CA Full-Time $90,000 - $120,000 Job Details If you are a Sr. Regulatory Affairs Specialist with experience, please read on! We are located in San Jose, CA and are a major player in the Medical Device Industry. We are currently looking to hire a very experience Regulatory Affairs...
Rapidly expanding Medical Device company with local roots in San Diego, CA is seeking to hire an all-around unique Lead Regulatory Affairs Specialist to prepare and monitor global submissions for acquisition of appropriate commercial distribution clearances in an expeditious manner. This will be a full time position based out of the San Diego headquarters, offering up to a $120k base salary with a...
Pharmaceutical and Research organization looking for a Senior Regulatory Affairs Specialist to join their team in Los Angeles, CA. Responsibilities: Prepares, submits, and maintains regulatory filings with relevant health authorities Participates in product development teams and creating of Regulatory Strategies Maintains country specific site registration requirements; Provides prompt evalua...
Job Summary Responsible for assisting the team with regulatory filings as necessary to market Zimmer products. This is an experienced level position, providing training towards full competency in Regulatory Affairs (RA). This position requires an intermediate understanding of Zimmer products and their use as well as an understanding of the regulatory admissions process. Works under minimum superv...
Regulatory Affairs Specialist, P/T or Consultant, Flexible Hours DiamoDent, Inc. is a dental manufacturer located in Anaheim Hills seeking for a part time or local consultant Regulatory Affairs Specialist. The ideal candidate must have strong background with minimum of 7 years experience with FDA Quality Regulations, ISO 13485, CMDCAS, FMEA, Design Reviews, MDR and etc. He or she must have experi...
Rapidly expanding Medical Device company with local roots in San Diego, CA is seeking to hire an all-around unique Lead Regulatory Affairs Specialist to prepare and monitor global submissions for acquisition of appropriate commercial distribution clearances in an expeditious manner. This will be a full time position based out of Orange County, offering up to a $120k base salary with a competitive ...
CyberCoders Search. Apply. Done. Learn more about CyberCoders Regulatory Affairs Specialist Apply San Diego, CA Unspecified Job Details Based in San Diego, CA we are an established medical device diagnostic company! Currently, we are in need of a Regulatory Affairs Specialist to join our team and help us meet the demands of our customers! What You Will Be Doing • Prepares, submits, and m...
Overview: The position Regulatory Affairs Specialist I reports to the Supervisor, and is responsible for the development, retrieval and maintenance of regulatory submissions. This position will work closely with the Supervisor in the preparation of submissions (notifications & registrations) for new products, product changes, as required to ensure continued compliance, and timely approval for mar...
Overview: The position of the Regulatory Affairs Specialist 2 is responsible for the development, retrieval and maintenance of regulatory submissions. Responsibilities: Manage assigned product brands in line with Product Development/Marketing Brand Managers Review and approve formulas, raw materials and other product design criteria. Assist in preparing and maintaining domestic and internatio...
Overview: This position supports the activities of the Regulatory group(s) with particular emphasis on submission preparation, publishing and regulatory information management. Responsible for planning and coordinating submission projects in accordance with company goals and priorities, and in collaboration with Regulatory submission managers. Responsible for global Health Agency submission compi...
Our Company is an R&D company specializing in non-invasive electrophysiological measurement systems. Our work builds on our revolutionary wearable biosensors and advanced algorithms to produce systems that monitor cognitive and physiological states for medical, military, and consumer applications. Our company is a small company with less than 20 employees, most of whom are Ph.D. level scientists...
Job Description: Quest is seeking a Regulatory Affairs Specialist who will be responsible for successfully implementing and scaling the company’s global regulatory and compliance program to support bringing our products to the market globally. The role will ensure that Quest is in compliance with all applicable domestic and international laws, regulations and customs for key markets at both the i...
Job Description: Senior Regulatory Affairs Specialist Ajulia Executive Search Located near Lexington Hills, California COMPENSATIONCompetitive Salaries, Full Benefits, Bonus Eligible, Relocation and Interview Travel Assistance Available RESPONSIBILITIES · Develop and implement regulatory goals for research goods and supporting the engineering projects · Organizes/ directs the preparation for regu...
About us Description The Regulatory Affairs Specialist is responsible for support of a variety of regulatory activities and projects with oversight from senior regulatory staff with such tasks and deliverables including product registrations and other related regulatory activities. The scope of the position will support BDB product platforms for IVD and Research product portfolios. Activities ...
Endologix develops and manufactures minimally invasive treatments for aortic disorders. We offer a dynamic, growth environment, competitive compensation and benefits, and a challenging, fulfilling experience in a fast-paced, growing company. Medical device professionals have the opportunity to develop and further their careers in a dynamic company that features the latest innovations in endovascul...
Job Description: Summary: Regulatory Operations team member in the Authoring Support Group (ASG) responsible for formatting of regulatory submission documents ensuring that documentation meet our clients submission-ready standards under direct supervision. Responsibilities: · Convert MS Word documents in a legacy format to ISIWriter using a custom conversion tool, ensuring that the correct styles...
Description The Regulatory Affairs Specialist is responsible for support of a variety of regulatory activities and projects with oversight from senior regulatory staff with such tasks and deliverables including product registrations and other related regulatory activities. The scope of the position will support BDB product platforms for IVD and Research product portfolios. Activities include bu...
Allergan plc (NYSE: AGN) is a bold, global pharmaceutical company and a leader in a new industry model – Growth Pharma. Allergan is focused on developing, manufacturing and commercializing branded pharmaceuticals and biologic products for patients around the world. Allergan markets a portfolio of best-in-class products that provide novel treatments for the central nervous system, eye care, medical...