Regulatory Affairs Intern - Hyderabad, Telangana

We are looking for a highly motivated and detail-oriented individual to join our team as a Regulatory Affairs Intern in a reputed Pharma Company. · Strong understanding of regulatory requirements governing the pharma industry, including FDA, EMA, and other relevant agencies. · Ex ...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. · ...

The Associate in the Office of Global Affairs (OGA) supports the universitys internationalization efforts by managing administrative operations... · ...

+As an internal medical / technical / scientific resource, leads medical affairs objectives in the affiliate country. · + · +Minimum 2-3 years post-qualification work experience in Medical affairs function. · Demonstrated ability to learn quickly and convey clinical and non-clini ...

Prepare dossiers for regulatory submissions including DMFs and variations review and prepare responses to queries from regulatory authorities during product registration and post-marketing phases coordinate with cross-functional teams for timely submission of dossiers maintaining ...

Job summaryWe are seeking a dynamic and strategic Corporate Affairs Manager to oversee and manage the companys interactions with internal and external stakeholders. · Government Affairs: · Serve as the primary liaison between the company and government authorities, · Monitor regu ...

We are seeking an experienced regulatory affairs expert as our new Senior European Regulatory Affairs ManagerOur team will be responsible for managing registration projects across EuropeWe are looking for someone who has experience in dossier compilation and coordination activiti ...

We are seeking a Regulatory Affairs Specialist to assist Compliance and Regulatory Affairs department management in executing day-to-day tasks associated with managing, maintaining and continually improving Imaging Endpoints' regulatory systems to meet regulatory requirements. · ...

I'm looking for a Regulatory Affairs Specialist to oversee the preparation and submission of regulatory dossiers ensuring compliance and timely approvals. · ...

The Vice President – International Business & Regulatory Affairs is responsible for driving global business expansion managing international export operations and ensuring regulatory compliance across multiple geographies. · Bachelor s degree in Science with an MBA in Marketing · ...

The Vice President – International Business & Regulatory Affairs is responsible for driving global business expansion, managing international export operations, and ensuring regulatory compliance across multiple geographies. The role combines strategic leadership, commercial grow ...

We are looking for a seasoned leader to drive our International Business Development and Export Operations. · ...

We are looking for a highly skilled and experienced Regulatory Affairs professional to join our team at Appidi Healthcare. · The ideal candidate will have a strong background in regulatory affairs and be able to ensure compliance with industry regulations. · ,Develop and impleme ...

Azurity Pharmaceuticals seeks a Medical Information Manager to oversee internal and external communication on its products. · ...

The Asst Manager/Manager/Sr Manager- Medical Affairs (Emerging Markets) will support the initiation, oversight and follow up of clinical studies and medical projects initiated within the therapeutic area for which he/she carries responsibility. · ...

The Regulatory Affairs professional will manage regulatory submissions and lifecycle activities for US FDA and Health Canada markets. · ...

We are looking for a Regulatory Affairs Specialist to join our API Division. This role is critical to ensuring compliance with regulatory requirements for our active pharmaceutical ingredients (APIs). The ideal candidate should have 1-7 years of regulatory affairs experience in t ...

The Regulatory Affairs Specialist role is critical to ensuring compliance with regulatory requirements for our active pharmaceutical ingredients (APIs). The ideal candidate should have 1-7 years of regulatory affairs experience in the pharmaceutical industry. · ...

To manage and support regulatory submissions approvals lifecycle maintenance of pharmaceutical products in ROW markets ensuring compliance with local regulatory requirements and company timelines. · Prepare review submit regulatory dossiers CTD ACTD country-specific formats for p ...

We are looking for a highly skilled and experienced professional to join our team as a Drug Safety Associate at Thepharmadaily LLP. · ...