Regulatory Affairs Coordinator

About the RoleWe are seeking a highly skilled Regulatory Affairs Analyst to join our team in Mexico City. As a key member of our Regulatory Affairs department, you will play a crucial role in supporting the preparation and submission of dossiers for new registrations, variations, and other regulatory submissions.ResponsibilitiesSupport the Regulatory Affairs...

Expand patient access to life-changing medicines and vaccines with PfizerWe're pushing boundaries in the pursuit of excellence and integrity. To achieve this, we need a dedicated Regulatory Affairs Expert Clinical Trials Coordinator who can navigate the ever-changing regulatory landscape.You'll be working closely with key stakeholders to ensure smooth...

We're a global network of innovative professionals who drive the development and delivery of life-saving therapies to patients worldwide. At PPD, we foster a collaborative culture that encourages strategic thinking, expertise, and seamless communication.**Job Summary:**This pivotal role is responsible for providing cutting-edge regulatory solutions and...

Job SummaryWe are seeking a highly skilled Regulatory Affairs Export Specialist to join our team at Solventum. This role will be responsible for providing regulatory support to Consultants and Distributors in Export Countries, ensuring compliance with local regulatory legislation and company requirements.Key Responsibilities:Provide regulatory support to...

We are seeking a highly skilled Regulatory Affairs Specialist to join our team in Ciudad de México, Mexico. As a key member of our regulatory affairs department, you will play a critical role in ensuring the compliance and registration of our medical devices in Latin America.The ideal candidate will have a minimum of 8-10 years of experience in regulatory...

Job SummaryWe are seeking an experienced Global Regulatory Affairs Strategist to join our team at Tether Operations Limited. The successful candidate will be responsible for designing and executing global regulatory strategies for our Tether Data business vertical.

We are seeking a skilled Regulatory Affairs Manager to join our team at Johnson & Johnson in Mexico City, MX; Mendoza, AR; Bogotá, CO or São Paulo, BR. This role will be responsible for the preparation, submission, and maintenance of filings.Key Responsibilities:• Collaborate with senior department members to expedite commercialization of new...

As a Regulatory Affairs Consultant at Icon, you will be joining the world's largest and most comprehensive clinical research organisation, powered by healthcare intelligence.What You Will Be DoingYou will contribute to the success of our organisation by ensuring compliance with regulatory requirements and developing strategic partnerships.Key...

Unlock your career aspirations and grow with Abbott Laboratories, a global healthcare leader.We're looking for a talented Regulatory Affairs Specialist to join our team in Mexico City. As a key member of our Regulatory Affairs department, you'll play a crucial role in ensuring compliance with regulatory requirements for our medical devices portfolio in Latin...

Job SummaryWe are seeking a highly skilled Regulatory Data Coordinator to join our team at Icon Plc. This role involves managing and maintaining regulatory data, ensuring it is accurate, up-to-date, and compliant with global regulatory requirements.About the RoleThis position is responsible for supporting the preparation, organization, and submission of...

Regulatory Affairs Specialist Job DescriptionKey Responsibilities:Prepare dossiers for drug products, ensuring compliance with COFEPRIS regulations.Coordinate with manufacturers and regulatory authorities to ensure product compliance.Develop risk management plans for new molecules and submit reports to regulatory authorities.Provide market research and...

Job DescriptionWe are seeking an experienced Regulatory Affairs Specialist to join our team in Mexico. As a key member of our regulatory affairs group, you will play a critical role in ensuring compliance with local regulations and standards for medical devices in the LATAM region.Main Responsibilities:Develop and implement effective regulatory strategies...

As a Regulatory Affairs Specialist at Abbott Laboratories, you will play a pivotal role in ensuring compliance with regulatory requirements for the company's medical devices portfolio. With a focus on Mexico City, you will be responsible for coordinating and managing all related RA local activities within the LATAM RA local regional team.About the...

Tether Operations Limited, a pioneering company in the stablecoin and blockchain industry, is seeking an experienced professional to join our team as Global Regulatory Affairs Strategist. This role is crucial in designing and executing global regulatory strategies for our Tether Data business vertical.About UsWe are committed to innovation and leadership in...

As a Regulatory Affairs Specialist at Icon, you will be part of the world's largest and most comprehensive clinical research organisation, driven by healthcare intelligence.**What you will be doing**:Contributing to the development of regulatory strategies and plans to ensure compliance with relevant regulations and guidelines.Collaborating with...

Company OverviewGE Healthcare is a leading innovator in medical technology and digital solutions with over 100 years of experience in the healthcare industry.We have approximately 50,000 employees worldwide and are dedicated to improving patient outcomes through our innovative products and services.Job DescriptionThis role requires an experienced Senior Ra...

HSBC is a leading financial institution with a global presence.We are currently seeking an experienced Compliance Regulatory Affairs Specialist to join our team in Mexico.The ideal candidate will have a strong command of English and be able to interpret regulations.The role requires attention to detail, good analytical skills, and strong interpersonal skills...

Job DescriptionWe are seeking a skilled Regulatory Affairs Specialist to join our team at Pfizer. This role will involve coordinating and executing activities related to drug product submissions and license maintenance to health authorities.Responsibilities:Coordinate and execute activities related to dossier planning and submission, including initial...

Job Description:">Manage global regulatory submission projects and contribute to the technical regulatory strategy for developing and registering products worldwide.Collaborate with internal teams and external contacts to implement global systems, tools, and processes supporting product development and market expansion.Represent Novartis on specific projects...

About Abbott LaboratoriesAbbott Laboratories is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future, anticipating changes in medical science and technology.Working at Abbott LaboratoriesAt Abbott Laboratories, you can do work that matters, grow, and learn, care for yourself and family,...