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Regulatory Affairs Specialist Jobs in Florida

14 jobs

Job Summary Works with a high level of autonomy to bring medical devices to market and ensure ongoing compliance while providing expertise and mentoring to less experienced colleagues in the development of their regulatory skills. Participates on cross-functional teams, develops global regulatory strategies, authors/reviews/approves regulatory submissions, interacts with regulatory agencies/notif...
Requisition ID 13862BR Job Title Principal Regulatory Affairs Specialist Group Orthopaedics Division Reconstructive Business Unit RCNCQR Business Function Regulatory Affairs Country United States State/Province FL City Fort Lauderdale Employment Category Full Time Percent Travel Required Up to 20% Shift 1st About Stryker Stryker is one of the world’s leading medical technology companie...
Oscor Inc. is a global US based medical device company headquartered in Palm Harbor, Florida. Oscor designs, manufactures and sells a variety of highly specialized implantable cardiac pacing leads, venous access systems and diagnostic catheters with sales to over 70 countries internationally. As a leading manufacturer of medical devices in the area of cardiology, electrophysiology and radiology, O...
Job Description: JOB DESCRIPTION Position type : Full-Time Location : Tampa, FL Top reasons to work for my client, Romark Laboratories: Do you want to work for an innovative company that explores molecules & treats infectious diseases/cancers. Do you want to work for a company that provides tremendous career advancement opportunities. Do you want to work for a company that offers health, dental, ...
Job Summary Works with a high level of autonomy to bring medical devices to market and ensure ongoing compliance while providing expertise and mentoring to less experienced colleagues in the development of their regulatory skills. Participates on cross-functional teams, develops global regulatory strategies, authors/reviews/approves regulatory submissions, interacts with regulatory agencies/notif...
Requisition ID 13862BR Job Title Principal Regulatory Affairs Specialist Group Orthopaedics Division Reconstructive Business Unit RCNCQR Business Function Regulatory Affairs Country United States State/Province FL City Fort Lauderdale Employment Category Full Time Percent Travel Required Up to 20% Shift 1st About Stryker Stryker is one of the world’s leading medical technology companie...
Requisition ID: 26182 Title: Regulatory Affairs Specialist Division: Arthrex, Inc. (US01) Location: INC- Naples, FL (US08) Main Objective: Supports Regulatory Affairs activities for Arthrex, Inc. Essential Duties and Responsibilities: With minimal supervision, prepares and submits regulatory applications to secure worldwide product approvals. Develops regulatory strategies in accordanc...
Requisition ID: 26182 Title: Regulatory Affairs Specialist Division: Arthrex, Inc. (US01) Location: INC- Naples, FL (US08) Main Objective: Supports Regulatory Affairs activities for Arthrex, Inc. Essential Duties and Responsibilities: With minimal supervision, prepares and submits regulatory applications to secure worldwide product approvals. Develops regulatory strategies in accordance wi...
Regulatory Affairs Specialist Job Summary Provides regulatory input for new product and sustaining engineering project teams; developing a regulatory strategy for global commercialization of products. Capable of identifying both domestic and international regulatory requirements early in product life cycles and coordinating the product registrations to meet company milestones and initiatives. Pr...
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 supervision. Princ...
DescriptionI. Department Overview: Regulatory Affairs supports the organization’s ability to market drugs throughout the development lifecycle by interacting with internal colleagues in Business Development, R&D, site RA; Regulatory Agencies; and Customers. Regulatory Affairs interacts with stakeholders by providing regulatory guidance throughout the product lifecycle, preparing and reviewing regu...
Regulatory Affairs Specialist Department: Regulatory Affairs - 067 Schedule: Full Time Shift: Days Hours: 8AM - 5PM Salary Range: Job Details: POSITION SUMMARY: · Manage assigned regulatory submissions including registration strategy, timeline and submission coordination, development/review of documentation, submission tracking, and liaison with submitter/regulatory authorities. Support di...
POSITION SUMMARY: · Manage assigned regulatory submissions including registration strategy, timeline and submission coordination, development/review of documentation, submission tracking, and liaison with submitter/regulatory authorities. Support distributors and business partners in securing and maintaining regulatory clearances. Maintain systems for tracking current projects and for projection f...
Overview: AMAZING INDIVIDUALS WORKING FOR POSITIVE PEOPLE at AIDS Healthcare Foundation! Does the idea of doing something that really makes a difference in people’s lives while being well-compensated intrigue you? Are you looking to work for an organization that encourages growth and success from each and every one of its employees? If so, AIDS Healthcare Foundation is the place for you! Found...