A company is looking for a Regulatory Affairs Specialist to support US and OUS regulatory activities for Class II and III products.
Key Responsibilities : Participate in product development teams to provide regulatory supportCompile technical documentation for global regulatory submissions and registrationsReview QMS and product changes for compliance with regulatory requirementsRequired Qualifications : Bachelor's Degree in STEM, Medicine, or Life Science1-2 years of experience in medical device product development or related fieldsFamiliarity with medical device regulations in the US and / or EUKnowledge of relevant standards and guidance documents (e.
g., 21 CFR 820, MDR)Experience in regulatory affairs, clinical affairs, Quality, or Engineering is required
Regulatory Affairs Specialist
We’re looking for a Regulatory Affairs Specialist with fragrance regulatory experience to join our team in the northern Fort Lauderdale area. Regulatory Affairs Specialist - Fragrance Industry. Minimum of 3 years of regulatory affairs experience, specifically within the fragrance or consumer g...
Regulatory Affairs Specialist
The Regulatory Affairs Specialist position entails managing diverse regulatory information and legal documentation requests from both internal and external stakeholders. These stakeholders include but are not limited to sample labs/shipping, production/logistics, customer service, perfumers, evaluat...
Regulatory Affairs Specialist
A company is looking for a Regulatory Affairs Specialist I to manage regulatory documentation and submissions. ...
Clinical Research Regulatory Specialist (experience in submissions to IRB)
The Regulatory Specialist will be responsible for ensuring regulatory compliance and keeping current with regulatory requirements. The Regulatory Specialist will also be responsible for using analytical skills to interpret complex regulations, communicating regulatory changes to stakeholders, and ov...
Behavioral Health Compliance Specialist
We are looking for a Behavioral Health Compliance Specialist to join our team! As a Behavioral Health Compliance Specialist, ensuring legal and ethical practices, promoting client quality care and safety, following all relevant internal rules and regulations, and carrying out the company mission wil...
Program Manager II - Vendor Management
A company is looking for a Program Manager II - Vendor Management. ...
Manager / Senior Manager, Compliance & Reporting Specialist
Manager / Senior Manager, Compliance & Reporting Specialist. Work with KPMG's extensive network of specialists & enjoy access to our Ignition Centers, where deep industry knowledge merges with cutting-edge technologies to create innovative tax solutions. KPMG is currently seeking a Manager / Senior ...
Senior Program Manager (Urinalysis)
Lead high visibility programs utilizing your experience and the Danaher Business System (DBS) tools to maximize efficiency and quality for critical-to-the-business product launches, communicate budget, schedule, resources, and performance to QCD (Quality, Cost, Delivery) metrics for the programs you...
Program Manager
The Program Manager serves a vital leadership role within the program and is responsible for management of canvass programs. He/She provides strategic guidance to teams and managers in ways to effectively deliver the program outcome to our organization. ...
Independence Compliance – Sr. Analyst
Compliance Senior Analyst, Independence Consultation – Business Relationships, Independence & Conflicts Network (ICN). Do you have a focus on compliance with regulations and policies? Are you passionate about quality-assurance and risk-management in a professional services environment? Then our Inde...