The Position As our Regulatory Affairs Manager, you will play a critical role in ensuring patients continue to have access to innovative healthcare solutions. You will lead and execute local regulatory activities aligned with regional strategies and
We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it’s no small feat. It takes
We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it’s no small feat. It takes
As a key member of the Government Affairs and Partnerships business unit of IIX, you will help drive key stakeholder relationships, business development, and support the strategic direction of the team for long term growth and profitability.
As a Senior Associate with the Government Affairs and Partnerships team at IIX, you will be given opportunities to design and implement development programs, support business development, contribute to strategic research and knowledge outputs, and facilitate key
Job Description: Job Responsibilities Government Affairs & State Liaisoning (Primary Responsibility) Develop and execute Mars Pet Nutritions Telangana Government Affairs strategy aligned with business priorities. Build and independently maintain trusted relationships with senior officials across Telangana Government departments
Senior Regulatory Specialist I – Toxicology, Global Regulatory Affairs (GBS) Location: Pune, India Function: Global Business Solutions (GBS) Department: Global Regulatory Affairs – Global Toxicology Team Reports To: Global Toxicology Team Lead, Global Regulatory Affairs Job Overview Join Ecolab
We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it’s no small feat. It takes
We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it’s no small feat. It takes
Overview: Dozee Health AI is a pioneer in Contactless Remote Patient Monitoring (RPM), proven to drive transformation at scale. Headquartered in Bengaluru, India, Dozee has emerged as India’s no. 1 RPM Company. We are seeking visionary
The Senior CRA will provide operational and administrative support to global clinical trial teams involved in New Chemical Entity (NCE) development programs. The role involves coordination of clinical trial documentation, regulatory submissions, site and vendor communications,
Position Title: Medical Writer, Clinical Development Role Summary: The Medical Writer will be responsible for authoring, reviewing, and managing high-quality clinical and regulatory documents to support global clinical development programs. The individual will work closely with
JOB PURPOSE The Head – Corporate Affairs at GMR Energy Group is responsible for managing strategic relationships, driving corporate engagement, facilitating regulatory clearances, revenue realization, and strengthening institutional networks. The role also focuses on reputation management, crisis
JOB PURPOSE The AGM- Corporate Affairs is responsible for driving the strategic positioning and stakeholder engagement initiatives of the organization within the energy sector. The role is responsible for overseeing government and industry relations, and public policy
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms
Job Description SummaryProvides regulatory strategy and direction to the business regarding healthcare industry regulatory requirements for product launch, premarket submissions/registrations and postmarket compliance, working closely with healthcare regulatory bodies globally. Interprets simple internal and external business challenges
SQR: Systems, Quality & Regulatory (SQR), a global function within Care Enablement ensuring Fresenius Medical Care’s products meet the highest standards of quality, safety, and regulatory compliance throughout the entire product lifecycle. The team supports market
Who We Are ABOUT ENOVIS Enovis Corporation (NYSE: ENOV) is an innovation-driven medical technology growth company dedicated to developing clinically differentiated solutions that generate measurably better patient outcomes and transform workflows. Powered by a culture of
Overview ROLE AT A GLANCE: The Supervisor – Public Affairs will support the Public Affairs team in day-to-day coordination, documentation and follow-up activities across regulatory, FSSAI, Direct Selling Monitoring Mechanism, Consumer Affairs, vendor management, special projects and internal processes.This