Regulatory Affairs Manager

**Regulatory Affairs Manager Central & Latin America** Are you passionate about R&D? Would you like to join us and take a front seat in our R&D team based in Mexico City As our Regulatory Manager you will be working as part of a passionate Regulatory team with a can-do mentality, reporting to the Regulatory Affairs Leader for Emerging Markets. You will...

**Overview** At the heart of QIAGEN’s business is a vision to make improvements in life possible. We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many initiatives and to our presence across the...

A Regulatory Affairs Associate must have a knowledge of the organization´s basic consulting models and methodologies as well as basic knowledge of what services the department provides. A Project Leader must be technically competent and continually developing the skills as defined in the department, under general direction of his/her Line Manager and...

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s...

About the Role\As a Regulatory Affairs Leader at Novartis Farmacéutica, you will play a crucial role in ensuring compliance with regulatory requirements and maintaining the technical documentation change system.\The ideal candidate will have experience managing global regulatory submission projects, providing strategic input on regulatory strategy,...

**Regulatory Affairs Analyst** **Your task and responsabilities** - Support to the Regulatory Affairs area in the preparation and submission of dossiers for new registrations, variations, FSC and others. - Support to Clinical Operations on the submission of clinical research protocols and amendments. - Responsible for the submission of the advertising...

Regulatory Affairs Coordinator **Category**:Reg Affairs & Safety Pharmacovigilance**Location**:Ciudad de México, Ciudad de México, MX**Position for Novo Nordisk GBS Mexico**- Join Novo Nordisk for a life-changing career establishing and developing a world-class Global Business Service Centre in Mexico City.- This will impact millions of people living with...

**Regulatory Affairs Specialist, Mexico (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 health, material...

Job DescriptionWe are seeking a highly skilled Regulatory Affairs Specialist to lead our North American team. As a key member of our regulatory affairs department, you will be responsible for ensuring compliance with local, regional, and ICH regulations. Your expertise will play a critical role in supporting product development from preclinical stages...

Senior Regulatory Affairs Specialist - Mexico City - Office with Flex ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development JR123070 Senior Regulatory...

Job Description: Regulatory Affairs Specialist, Mexico (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 health,...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life Lead and prepare RA meetings (regulatory status) involving the OU's under their responsibility....

Senior Regulatory Affairs SpecialistWe're seeking a highly skilled Clinical Trials Regulatory Affairs Expert to join our team at ICON Plc. This is an exciting opportunity to leverage your expertise in regulatory affairs and contribute to the success of our clinical trials.About the Role:Lead the preparation, submission, and maintenance of regulatory...

El **ESPECIALISTA SR. DE ASUNTOS REGULATORIOS** ayudará en las actividades regulatorias de productos para dar soporte a nuestra empresa **Competencias**: - Garantiza el mantenimiento de los productos asignados y autorizados mediante la presentación oportuna de prórrogas y modificaciones a las condiciones de registro sanitario. - Para productos y...

**Overview** At the heart of QIAGEN’s business is a vision to make improvements in life possible. We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many initiatives and to our presence across the...

Regulatory Affairs Specialist Job description: Full time On-Site, 9:00AM to 6:00PM in Polanco CDMX, Mexico Immediate job! Chemist/ Biologist and also Pharmacist Diploma in order to act as sanitary responsible Experience in Dossier preparation for Drug products: take care of the preparation of your dossier. Printing, submitting. Including preparations of...

Responsible for coordinating, preparing, and maintaining regulatory submissions and documents on a global level for Europe, the United States, and other countries. Primary responsibilities are to ensure regulatory compliance for assigned product lines Other responsibilities include coordinating recalls, identifying relevant standards and guidance documents...

Regulatory Affairs Specialist Job description: Full time On-Site, 9:00AM to 6:00PM in Polanco CDMX, Mexico Immediate job! Chemist/ Biologist and also Pharmacist Diploma. Experience in Dossier preparation for Drug products: take care of the preparation of your dossier. Viewing, checking, preparing for submission to COFEPRIS, Printing, submitting. At least 1...

About the RoleWe are seeking a highly skilled Regulatory Affairs Expert to join our team at Worldwide Clinical Trials.Job DescriptionIn this role, you will be responsible for planning, initiating and tracking documents required for regulatory submissions. You will also be involved in collecting essential documents, reviewing country/site/EC requirements, and...

Regulatory Affairs Specialist Job description: Full time On-Site, 9:00AM to 6:00PM in Polanco CDMX, Mexico Immediate job! Chemist/ Biologist and also Pharmacist Diploma. Experience in Dossier preparation for Drug products: take care of the preparation of your dossier. Viewing, checking, preparing for submission to COFEPRIS, Printing, submitting. At...