Regulatory Affairs Specialist

**About Us**Galderma is a leading dermatology company with a rich legacy and a commitment to innovation. We are dedicated to advancing dermatology for every skin story.**Job Summary**We are seeking a highly skilled Regulatory Affairs Specialist to join our team. As a Regulatory Affairs Specialist, you will be responsible for implementing regulatory programs,...

About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Galderma. As a key member of our regulatory team, you will be responsible for implementing regulatory affairs programs, processes, and policies to support our product regulatory activities.Key ResponsibilitiesDevelop and implement regulatory affairs programs and...

About Zimmer BiometZimmer Biomet is a global medical technology leader with a rich history of innovation and commitment to improving patient outcomes. With a presence in nearly 100 countries, our products and technologies enhance patient mobility and quality of life.Our MissionWe are dedicated to providing mobility and renewed life to people around the...

{"h1": "Join Galderma's Regulatory Affairs Team", "p": "At Galderma, we are committed to advancing dermatology for every skin story. As a Regulatory Affairs Coordinator, you will play a critical role in implementing regulatory programs, processes, and policies to support our innovative products and services.Your key responsibilities will include: *...

Regulatory Affairs Manager - SAM RegionThe Regulatory Affairs Manager - SAM Region plays a key role in leading the planning and execution of regulatory activities for development, registration, and post-authorization initiatives in the SAM region (South America, Andean Region, and Mexico). Key responsibilities include:Developing and implementing regulatory...

Company Overview: Galderma stands as a leader in dermatology, with a legacy of innovation and a presence in around 90 countries. Our commitment to delivering a science-driven portfolio of premium brands and services spans the dynamic dermatology market, encompassing Injectable Aesthetics, Dermo-cosmetics, and Therapeutic Dermatology. Since our inception in...

About Zimmer BiometZimmer Biomet is a global medical technology leader with a nearly 100-year history of innovation. Our mission is to enhance patients' mobility and quality of life through our products and technologies.Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory team, you will...

Job DescriptionRegulatory Affairs Manager - Latin AmericaWe are seeking a highly skilled Regulatory Affairs Manager to join our team in Latin America. As a key member of our regulatory team, you will be responsible for ensuring compliance with regulatory requirements and developing strategies to advance projects in the region.Key Responsibilities:Prepare,...

About Zimmer BiometZimmer Biomet is a global medical technology leader dedicated to enhancing patient mobility and quality of life. With a rich history spanning nearly 100 years, our company has been at the forefront of innovation, driving advancements in medical technology that make a meaningful difference in people's lives.Our MissionWe are committed to...

Company Overview: Galderma is a leading entity in dermatology, recognized for its innovative contributions and a legacy that spans decades. Our commitment to advancing dermatological care is evident in our diverse portfolio, which includes Injectable Aesthetics, Dermo-cosmetics, and Therapeutic Dermatology. We operate in around 90 countries, focusing on the...

Company Overview: Galderma is a global leader in dermatology, dedicated to advancing the science of skin health. With a presence in around 90 countries, we focus on delivering innovative products and services across various dermatological segments, including Injectable Aesthetics, Dermo-cosmetics, and Therapeutic Dermatology. Position Overview: The...

Job Description Summary:Job Title: Contractor, Manager, Regulatory AffairsLocation: ColombiaWe are seeking a highly skilled Regulatory Affairs professional to collaborate with our team in leading the planning and execution of regulatory activities for development, registration, and post-authorization initiatives in the South America, Andean Region, and...

About the PositionWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Werfen. As a key member of our Quality Assurance department, you will play a critical role in ensuring the compliance of our products with regulatory requirements.Key ResponsibilitiesSupport the implementation and execution of regulatory and quality plans, and...

Job Title: QA RA SpecialistWerfen is seeking a highly skilled QA RA Specialist to support the implementation and execution of regulatory and quality plans, and perform any regulatory activities for products marketed by Werfen.About the PositionThe ideal candidate will have a strong background in Quality Assurance and Regulatory Affairs, with a minimum of 2...

Job Title: Regulatory Affairs Manager - Latin AmericaWe are seeking a highly skilled Regulatory Affairs Manager to join our team in Latin America. As a key member of our regulatory team, you will be responsible for ensuring compliance with regulatory requirements and developing strategies to advance projects in the region.Key Responsibilities:Prepare,...

Job DescriptionOrganon is seeking a highly skilled Pharmacovigilance and Regulatory Affairs Specialist to join our team in Colombia. As a key member of our Regulatory Affairs and Pharmacovigilance department, you will be responsible for ensuring compliance with local laws and regulations, managing Pharmacovigilance submission requirements, and executing...

About the PositionJob SummaryWe are seeking a highly skilled Quality Assurance and Regulatory Affairs Specialist to support the implementation and execution of regulatory and quality plans for products marketed by Werfen. The ideal candidate will have a strong background in Quality Assurance and Regulatory Affairs, with experience in the Medical Device...

About the RoleThis is a challenging and rewarding opportunity to join Takeda Pharmaceutical as a Regulatory Affairs Specialist. As a key member of our team, you will play a critical role in supporting the business strategic plan to obtain Marketing Authorizations, renewals, and variations for existing and new products.Key ResponsibilitiesSupport the...

At Zimmer Biomet, we are committed to advancing the field of medical technology and enhancing patient mobility. As a global leader in our industry, we strive to make a meaningful impact on people's lives.Key Responsibilities:Develop and implement regulatory strategies to ensure compliance with relevant laws and regulations.Collaborate with cross-functional...

About the RoleThe Regulatory Affairs Manager will lead a team of regulatory experts with complex projects. This role will work collaboratively with the business to seek efficiencies in the current team's operation, challenge the team to look for alternative regulatory strategies, and work hand in hand with the business as a whole. The manager will orient,...