Senior Director Regulatory Affairs - Watertown, MA

Company Overview · Founded in 1947, Pulpdent Corporation is an industry-leading dental research and development (R&D) and manufacturing company. Pulpdent's corporate headquarters, research laboratory, and manufacturing facilities are located in Watertown, Massachusetts, in the Bo ...

Site: The General Hospital Corporation · Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teach ...

Site: The General Hospital Corporation · Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teach ...

Site: The General Hospital CorporationMass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching ...

Overview: · Make a global impact—join Repligen. · We're united by a mission to inspire advances in bioprocessing as a preferred partner in the production of biologic drugs that improve human health worldwide. No matter your role or background, at Repligen, you will play a key par ...

Parexel International LLC seeks a Regulatory Affairs Consultant to prepare clinical and regulatory documentation for clinical trials. The position may telecommute from anywhere in the United States up to 5 days per week. · ...

Opportunity awaits those up to the challenge of developing transformative therapies across a broad range of debilitating diseases. · ...

The Director, Regulatory Affairs will be responsible for the strategic leadership, · development and execution of science-based, solution-oriented, · and globally aligned regulatory strategies for the program(s) · under his/her accountability.This role serves as a key · regulator ...

We are seeking a Regulatory Affairs Consultant to prepare clinical and regulatory documentation for clinical trials and deliver consulting services to ensure that the company meets regulatory requirements. · ...

· Overview · Make a global impact—join Repligen. · We're united by a mission to inspire advances in bioprocessing as a preferred partner in the production of biologic drugs that improve human health worldwide. No matter your role or background, at Repligen, you will play a key p ...

We are currently looking for an ambitious Principal Regulatory Affairs Specialist to join our Endovascular Robotics business within Advanced Therapies. · We believe the combination of endovascular robotics, image guidance, and dedicated devices will change the way neurovascular p ...

We are seeking professionals with the following required skills and qualifications to help us achieve our goals: · Bachelor's degree in Biological or Healthcare Science, with previous experience in similar strategic international regulatory affairs positions. · ...

Overview · Make a global impact—join Repligen.We're united by a mission to inspire advances in bioprocessing as a preferred partner in the production of biologic drugs that improve human health worldwide. No matter your role or background, at Repligen, you will play a key part in ...

Nazwa biura: USA - Maryland - Rockville, Durham Blackwell Street, USA - Massachusetts - Waltham, USA - Pennsylvania - Upper Providence · Posted Date: Feb · Business Introduction · At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion ...

At GSK, we have bold ambitions for patients, aiming to positively impact health of 2.5 billion people by end of decade. · We foster culture ambitious for patients, accountable for impact and committed doing right thing making sure focus efforts accelerating significant assets mee ...

We are looking for a Regulatory Affairs Specialist to develop and deploy innovative and compliant regulatory strategies across business and markets. · Assist in implementing comprehensive regulatory strategies by collaborating with regulatory subject matter experts (SMEs). · Coor ...

Job summary · Regulatory Affairs Manager for medical devices company. · Partner closely with the Director of Regulatory Affairs to define and implement regulatory strategies. · Provide regulatory guidance during product development to ensure compliance. · ...

We are seeking a Regulatory Affairs Specialist to support the Life Cycle Management (LCM) Regulatory Affairs team in the creation,maintenance,and review of technical documentation.This role ensures compliance with European and U.S.medical device regulations,includingsuch as EU MD ...

· Nearly 37 million Americans are currently affected by Chronic Kidney Disease. 37 million. · At Akebia we take that number very seriously and every day we come to work, with the purpose of bettering the lives of each person impacted by kidney disease and the renal community tha ...

+Job Summary · The VP of Regulatory Affairs will lead create and drive the regulatory strategy for life cycle management activities for Vafseo Auryxia and early development programs. · ...

The Regulatory Affairs Manager reports to the Director of Regulatory Affairs and is responsible for executing regulatory strategies, ensuring compliance with global regulations and leading the process to obtain and maintain market approval for DeepHealth's product and product dev ...