Principal Regulatory Affairs Specialist - Endoscopy. This role in Regulatory Affairs will be responsible for developing regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contract manufacturers. Responsible for preparation and subm...
Principal Regulatory Affairs Specialist - Endoscopy. Principal Regulatory Affairs Specialist – Endoscopy . This role in Regulatory Affairs will be responsible fordeveloping regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contrac...
In addition, this position will support the regulatory department by maintaining data within regulatory data systems, supporting regulatory projects and initiatives and by supporting ongoing regulatory operations. The Specialist, I - Regulatory Affairs will support the maintenance of EU MDR technica...
In addition, this position will support the regulatory department by maintaining data within regulatory data systems, supporting regulatory projects and initiatives and by supporting ongoing regulatory operations. The Specialist, I - Regulatory Affairs will support the maintenance of EU MDR technica...
Our client is currently seeking a Senior Regulatory Compliance Specialist. Monitor international standards and guide regulatory testing requirements. Assist with risk analysis and regulatory submissions. ...
The Regulatory Affairs Specialist will work closely with the Director of Regulatory Affairs to obtain and maintain global regulatory approvals to allow IPG to market its state of the art devices worldwide. The ideal candidate is a diligent, hardworking individual with 2 to 5 years of regulatory expe...
Principal Regulatory Affairs Specialist – Endoscopy . This role in Regulatory Affairs will be responsible for developing regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contract manufacturers. Responsible for preparation and sub...
A SharkNinja Associate Program Manager thinks, acts and leads his/her programs like a global leader for every project or program they manage and owns the overall success of the program with a steady focus on Scope, Cost, and Schedule. Associate Program Managers deliver sustainable, best in class pro...
The Director of Quality Assurance and Regulatory Affairs (QA/RA) is responsible for ensuring that Precision Optics Corporation's products meet applicable regulatory requirements and quality standards. Responsible for all quality assurance and regulatory functions across POC's Portland & Gardner site...
The Clinical Manager is responsible for the management and quality assurance of all clinical services of the program, including the training and supervision of all clinical staff. The Clinical Manager is a key leader on the Management Team and works closely with the Senior VP of Clinical Services to...
As the Associate Director of Regulatory CMC, reporting to the Director of Regulatory CMC, you will be pivotal in managing the development and submission of regulatory filings for gene therapy projects both domestically and internationally. Identify and articulate regulatory opportunities and challen...
The Program Events and Volunteer Manager collaborates with other program staff and community partners to ensure that the programming and support offered at Bethany Hill Place is responsive to resident needs. The Program Events and Volunteer Manager reports to the Executive Director and is responsibl...
Provide overall company leadership and direction for worldwide Tecomet Quality Assurance and Regulatory Affairs Systems, encompassing both improvements and sustaining activities. ...
They are seeking a dynamic Director of Regulatory Strategy to steer our groundbreaking projects through the complex regulatory landscape with vision and precision. Director, Regulatory Strategy. Bachelor's degree in a relevant life sciences field with at least 8 years of experience in the biopharmac...
Analyze and review test packets, creating detailed test logs to track quality assurance. Oversee multiple projects concurrently, ensuring that quality standards are consistently achieved. Address quality issues promptly and develop effective solutions. Create or update procedures for capturing, inve...
Oversee the delivery, implementation, and impact tracking of in-person, virtual, and online training programs tailored to diverse audiences, including firefighters, first responders, teens, young adults, and workplaces nationwide. Proactively manage client relationships, including prospecting, sched...
Are you a seasoned regulatory CMC leader looking for a new challenge? We are seeking a dynamic professional to lead a Global Regulatory Affairs CMC team in a top-tier biopharmaceutical company. This is a pivotal role that will shape global CMC regulatory strategies through all phases of product deve...
The Compliance Specialist assists the Director of Quality and Compliance with ensuring program adherence with licensure, accreditation, regulation, and government agency standards. Work in conjunction with the Director of QA and Compliance and Program Management to monitor compliance with action pla...
Senior Analyst to join our Compliance team! This is an exciting new opportunity for an individual to join a growing company and compliance team. Senior Analyst, Legal & Compliance. Act as a primary legal and compliance resource for business units, offering timely and accurate legal research and ...
We seeking a highly collaborative, proactive Customs & Trade Compliance Analyst to ensure our adherence to U. Manage and conduct import and export compliance audits, review corrective actions, evaluate broker/freight forwarder compliance and report monthly metrics. Identify and report to Bose Corpor...
Regulatory Affairs Leader (Associate Director). Bachelor's Degree (or internationally recognized equivalent) & minimum of 3 years experience in the pharmaceutical or biotechnology industry or with regulatory agencies; OR minimum of 7 years progressive regulatory affairs experience. The Regulator...
Senior Director of Quality, Regulatory and Clinical Affairs. The role will be responsible to work through multiple levels within the organization and external stakeholders to influence and drive Waters Quality, Regulatory & Clinical Affairs strategy to support Waters business growth and success ...
This includes developing and implementing regulatory strategies for product approvals, leading the registration of products, ensuring compliance with global regulatory requirements, and managing the regulatory affairs team. Title: Regulatory Affairs Manager. The Regulatory Affairs Manager will be re...
ES Project Managers are responsible for managing the execution of a broad array of projects for client or at a client sites/facilities. Project managers are the main point of contact to escalate issues and reports daily activity and to ensure a safe, compliant, and profitable project. As demand for ...
Prepares project estimates, proposals, and assists with contract preparation. Possess ability to follow through on projects to completion. ...