Regulatory Affairs Specialist III. The primary purpose of this position is to strategically plan, execute and provide oversight to regulatory activities. US, EU, ISO standards and other regulatory requirements based on geography. Responsible for planning, managing and implementing regulatory strateg...
Remote-Spanish-Speaking-Medical Device Regulatory Affairs Specialist II. As a Regulatory Affairs Specialist II you will:. Work with the international regulatory affairs group to ensure products are registered globally based on the spinoff strategy. Field requests from global regulatory associates fo...
Regulatory Affairs Specialist II. In this role, you will perform specialized level work assignments and/or analyses, evaluation, preparation, and submission of documentation for regulatory registration, ensuring products and procedures comply with regulatory agency specifications. Acts as a regulato...
The Senior Medical Safety Specialist works with minimal supervision on a range of medical safety activities of varying complexity in collaboration with Medical Safety team members and other functions, including Regulatory, Quality/Post-Market vigilance, Risk Management, Complaint Handling, Product D...
Remote-Spanish-Speaking-Medical Device Regulatory Affairs Specialist II. As a Regulatory Affairs Specialist II you will:. Work with the international regulatory affairs group to ensure products are registered globally based on the spinoff strategy. Field requests from global regulatory associates fo...
The Senior Regulatory Specialist is responsible for activities which lead to and maintain regulatory approval to market devices. Additionally, the Specialist is responsible for assessment of device changes for regulatory implications. You will have the opportunity to discuss your preferred working l...
The International Regulatory Affairs Specialist provides regulatory support for implantable neurostimulation therapy for the treatment of obstructive sleep apnea. Interact with international regulatory partners in local offices to support submission contents, as well as foreign regulatory agency rev...
Senior Regulatory Affairs Specialist. Acts as a regulatory representative on core product development teams, communicates regulatory requirements and impact of regulations to the development team. In this role, you will lead the preparation and submission for regulatory approvals and identify and re...
The Principal Regulatory Affairs Specialist will play a critical role in preparing comprehensive regulatory strategies for complex new devices and post market changes within Philips’ Ultrasound business. Develop regulatory strategies and communicate risks within regulatory strategies vs project plan...
The Senior Regulatory Affairs Specialist is responsible for planning, managing, and implementing regulatory submissions to the US FDA, EU notified bodies, as well as supporting world-wide product registrations. The position is also responsible for ensuring continued compliance with regulatory agency...
The Regulatory Associate is responsible for activities which lead, improve and drive efficiencies across regulatory product approval processes. Actively participate in various Quality System Community of Practice teams representing Regulatory Affairs interests, assessing impact, and bringing awarene...
The Regulatory Affairs Specialist will develop strategies and submissions for projects and issues related to regulatory documents, global submissions, investigations, product development planning, and regulatory agency interaction for blood products and biologics. Review and approve all labeling (pr...
The Specialist II is responsible for Regulatory Affairs support of global regulatory submissions for the BSC product development process, integration of acquired products, and ongoing regulatory compliance. Provides technical guidance and regulatory training/mentoring to other Regulatory Affairs emp...
As an Independence Program Manager, you would be responsible for supervision and training of Community Support Professionals and Community Support Specialists, oversight of program services delivery, completion of required documentation and data collection, among other tasks assigned by the supervis...
Residential Program Manager Description:. Residential Program Manager Responsibilities. Oversight of site operations and program service delivery including medication administration, coordination of medical appointments, meal planning/preparation, transportation, maintenance, implementation of progr...
Quality Assurance develops and implements a compliant and cost-effective quality system that assures products and services are reliable, safe and effective. This job family provides oversight of production/manufacturing activities, training to operational and quality control personnel, and educates ...
This role provides overall project management and leadership for one or more construction projects, or a portion of a large project, at any given time. This role is involved in managing all aspects of a project including planning, carry-out, and close-out of Egan Construction Projects specific to cu...
Program Manager to work in Ramsey, MN!. Defines when programs are to set up to manage multiple connected projects, and sets up the method and format for this program level management. Receives priorities and program or project specifics and generally can develop, plan and prioritize day to day activ...
The Program Manager will collaborate with various stakeholders, including LTC facilities, educational institutions, and community organizations, to develop and implement programs that address the unique challenges faced by New Americans entering the LTC careers. The New Americans in Long Term Care (...
The Program Manager (PM) maintains and expands relationships with customers. Be the lead to maintain productive, professional relationships with personnel in identified top tier MultiSource accounts and working closely with the Account Manager to grow the account. Coordinate internal stakeholders, i...
Layout and Composition Specialist, 508 Compliance. Layout and Composition Specialist, 508 Compliance. Remediate PDFs for 508 compliance to ensure they. Three years of experience with Section 508 compliance (PDF remediation). ...
The Project Manager will provide overall leadership direction to a project, including the management of project quality, timeliness, safety, as well as mentoring the project team. Develop and maintain project financial projections and equipment projections. Manage Assistant Project Manager(s) and Pr...
The Regulatory Affairs Manager is responsible for leading a team of Regulatory professionals with responsibility for developing strategies and executing on regulatory submissions to introduce new products and therapies and maintain existing products to global markets. Minimum 7 years experience in r...
The Lead Project & Program Manager (also referred to as Business Process Manager – Lead to Quote) is responsible for supporting initiatives across the Tax & Accounting Division. The Business Process Manager is responsible for developing and implementing standardized / best practices for Lead to Quot...
RCIS (Rural Crop Insurance Service), a division of Zurich North America, is currently hiring a Compliance Analyst and this person can work at either the Anoka, MN office in a hybrid schedule OR remotely for the right candidate. Reviews regulatory compliance internal controls and produces requested a...