Director, Device, Global Regulatory Affairs - Morrisville

The Regulatory Affairs Specialist will be responsible for a wide variety of regulatory activities for sustaining products including medical devices and Software as Medical Device (SaMD) and regulatory operation. · ...

The Director Regulatory Affairs provides operational leadership for the department overseeing innovative solutions including regulatory expertise and client interface to provide strategic regulatory intelligence and guidance for product development from preclinical through regist ...

Teleflex is investing in our capability to drive material cost improvement opportunities as part of a strategic corporate approach to reversing recent trends in cost escalation and generating significant stakeholder value. · ...

The Senior Director, CMC Global Regulatory Affairs is responsible for leading all regulatory CMC development, registration, and compliance activities from early development through commercialization. · Lead development of CMC and device regulatory submission strategies by working ...

The Associate Director Regulatory Affairs – CMC is responsible for preparing regulatory submissions to support clinical development registration lifecycle management assigned project including small molecules drug-device combinations. · ...

The Associate Director, Regulatory Operations & Projects is responsible for managing Liquidia's regulatory operations and regulatory infrastructure projects in the planning, coordination, · & execution of global regulatory submissions, document management activities, · & evolving ...

The Director Medical Affairs is a strategic leader within US Medical Affairs responsible for developing medical strategy driving evidence generation · Develop execute US Medical Affairs strategy for PAH brands pipeline programs aligned overall corporate product objectives · Cont ...

+The Regulatory Intelligence Manager will play a pivotal role in monitoring, analyzing, and communicating global regulatory developments that impact the client's pipeline and operations. · ...

Work Schedule · Standard (Mon-Fri)Environmental Conditions · OfficeJob Description · At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make t ...

We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. · We are agile and driven to accelerate the delivery of therapies, because we are passionate about changing lives. · Syn ...

We have successfully supported the top pharmaceutical companies and more than 750 biotechs in the last years. · ...

The QMS AI Quality & Compliance Specialist is responsible for supporting the implementation and operation of Thermo Fisher Scientific's AI Compliance Program within GxP-regulated environments.Apply established Quality standards, policies, and procedures to AI systems used in GxP- ...

The Head of R&D and Scientific Strategy leads medical and scientific contributions across clinical development programs and strategic partnerships in a TA. · The role will directly influence business growth through innovation and alignment. Develop strategies for exploring new in ...

The Assoc. Director / Director, Clinical Development Operations will have a strong blend of scientific knowledge, clinical operations and regulatory expertise., · ,Clinical Study Strategy & Oversight: · , Partner with the clinical team to design and execute diagnostic clinical s ...

The Assoc. Director / Director, Clinical Development Operations will have a strong blend of scientific knowledge, clinical operations and regulatory expertise, · Partner with the clinical team to design and execute diagnostic clinical studies supporting product development and re ...

The Director of Clinical Supply is responsible for the strategic planning, execution, and oversight of global clinical supply activities in support of clinical development programs. · ...

+Liquidia Technologies is seeking a Market Access Medical Science Liaison (MAMSL) to serve as a field-based scientific and strategic expert supporting managed care, Medicaid, and specialty pharmacy stakeholders involved in the access, education, and real-world utilization of YUTR ...

We Equip Clinicians With Some Of The Most Advanced Medical Devices On The Market Today, From Our World-class Brands Including The Arrow EZ-IO System that helps address the time-critical challenge of emergency vascular access, · and QuikClot and QuikClot Control+ hemostatic device ...

This role is responsible for creating biocompatibility evaluations and overseeing testing activities as necessary to support a variety of projects related to R&D and design control changes, · as well as special projects. ...

Expected Travel: Up to 10% · Requisition ID: 13446 · About Teleflex Incorporated · As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in healthc ...