Regulatory Affairs Coordinator

Job SummaryWe are seeking a skilled Regulatory Affairs Specialist to join our team at Pfizer.This role will support the Regulatory team in new product registration and post-approval changes, working closely with local and regional stakeholders to deliver efficient regulatory submissions and processes.The successful candidate will possess a thorough...

Lead Regulatory Affairs SpecialistWe are seeking an experienced Project Director to lead our Regulatory Affairs team in Colombia and Chile. As a key member of our Language Services department, you will play a critical role in expanding our business growth through Regulatory Labelling authorization services.Job SummaryThe successful candidate will have a...

Diversity, Equity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest...

Job Description: Regulatory Affairs Specialist, Chile (Export) (Solventum) 3M Health Care is now Solventum At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers’ toughest challenges, we pioneer game-changing innovations at the intersection of...

At Allergan, we strive to have a remarkable impact on people's lives across various key therapeutic areas – immunology, oncology, neuroscience, and eye care.Company OverviewOur mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow.We are committed to...

**Company Description** ArtiXio is a global consulting and services company specializing in Regulatory Affairs, Market Access, and Pharmacovigilance for pharmaceutical, biotech, cosmetics, medical device, and dietary supplements manufacturers. Our services cover compliance, regulatory intelligence in over 70 countries, regulatory operations, post-market...

At Guerbet, we build lasting relationships to enable people to live better. This is Our Purpose.We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, digital and AI solutions, for diagnostic and interventional imaging.As a pioneer in the field of contrast products since 95 years, we continuously...

Gracias por tu interés en trabajar para nuestra empresa. Contar con el talento adecuado es crucial para lograr nuestros objetivos. El 01 de abril de 2024, 3M Healthcare experimentó una separación corporativa que condujo a la creación de una nueva empresa denominada Solventum. Aún, estamos en el proceso de actualizar nuestra página de carreras y los...

387432BR **Regulatory Affairs Analyst**: Chile **About the role** 1.066.824. That’s the number of patients we reached in 2021. We want curious, courageous and collaborative people like you to join our inspiring environment. Here you’re given opportunities to make a genuine impact on our patient driven mission. Here you’re surrounded by people who...

**This is where you save and sustain lives** At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in...

Solventum, a pioneering healthcare company, is seeking a skilled Regulatory Affairs Specialist to join our team. With a legacy of creating breakthrough solutions, we're committed to improving lives through innovative healthcare products.About SolventumAt Solventum, we enable better, smarter, safer healthcare by partnering with the brightest minds in the...

Can you drive the global strategy for culture, engagement and performance management at Novo Nordisk? Do you have the interpersonal skills to navigate in a complex stakeholder landscape and are you able to motivate, set direction and deliver results? At Novo Nordisk, we are our people. And together we can make an impact. **The Position** **Main...

About Artixio Consulting Pvt LtdWe are a global consulting and services company specializing in Regulatory Affairs, Market Access, and Pharmacovigilance for pharmaceutical, biotech, cosmetics, medical device, and dietary supplements manufacturers. Our services cover compliance, regulatory intelligence in over 70 countries, regulatory operations, post-market...

**Job Description**: Regulatory Affairs Specialist, Export Countries (Solventum) - Chile or Colombia- 3M Health Care is now Solventum- At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers’ toughest challenges, we pioneer game-changing innovations...

About ICONICON plc is a world-leading healthcare intelligence and clinical research organization. We pride ourselves on fostering an inclusive environment that drives innovation and excellence, and we welcome talented individuals to join us in shaping the future of clinical development.Our company's success depends on the quality of our people, which is why...

Senior Project Manager Job DescriptionThe ideal candidate will have a proven track record of success in managing complex projects and teams, with a strong background in regulatory affairs labelling.We are seeking a highly experienced Senior Project Manager to join our team in Colombia and Chile. As a Senior Project Manager, you will play a key role in...

**Company Description** The mission of the Regulatory Affairs Manager is to lead the activities to register and maintain registration of oncology and specialty care products in Chile, cooperating with the Regional Manager, in alignment with business needs, to assure compliance with local regulations and with AbbVie policies. The Technical Director is...

Job OverviewWe are seeking a highly skilled Clinical Research Coordinator to join our Regulatory Submissions team at Medpace in Chile.Estimated Salary Range:$60,000 - $80,000 per year, depending on experience.Key ResponsibilitiesProvide day-to-day support to Regulatory Submission Managers and Start Up teams, ensuring deadlines are met.Conduct quality control...

Job SummaryA career opportunity has arisen within Medpace in Chile for a highly motivated and organized individual to join our Regulatory Submissions team as a Regulatory Submissions Coordinator. As a key member of the team, you will be responsible for providing day-to-day support activities, ensuring deadlines are met, and maintaining spreadsheets.This is...

Senior Project Manager OpportunityWe are seeking an experienced Senior Project Manager to join our team at ICON, a world-leading healthcare intelligence and clinical research organization.As a Senior Project Manager, you will play a crucial role in expanding our business growth within the Language Services team through Regulatory Labelling authorization...