Global Regulatory Affairs Expert

About The Zonal Group: As a global medical aesthetics organisation, we deliver an extensive product range with an in-house commercial infrastructure, including manufacturing and a network of distributors in leading global markets. Our products are sold in 55 countries worldwide.Job Description: We are seeking a Regulatory Affairs Specialist to manage the...

Job DescriptionWe are seeking a highly skilled Regulatory Affairs Expert to join our team. The ideal candidate will have a strong background in CMC Regulatory Affairs and experience with topical and/or systemic drugs.Key Responsibilities:Contribute to global regulatory CMC strategies.Assess regulatory impact of proposed CMC changes and contribute to the CMC...

About the Job: We are looking for a Regulatory Affairs Specialist to manage the global product registration and regulatory approvals for our Energy-Based Devices (EBD). In this role, you will ensure compliance with international regulatory authorities and support market entry for EBDs worldwide.Key Responsibilities:Manage complex projects and deliverables...

At Alira Health Group, we value innovation and initiative. Our global team is dedicated to collaboration, where physical boundaries don't limit, but encourage, mutual growth. We explore all contributions and new ideas with an open mind and drive our work by shared values: be courageous, be accountable, be honest, be inclusive, and elevate others.About the...

Job Details: We are seeking a highly skilled Pre-Market Regulatory Affairs Engineer to join our Corporate Regulatory Affairs Team at Sinclair EBD. The successful candidate will be responsible for ensuring regulatory requirements are met for new product development and design changes to established legacy devices.The Role: As a Pre-Market Regulatory Affairs...

**Company Overview**Sinclair is a global medical aesthetics organisation founded in 1971, delivering an extensive product range worldwide. With an in-house commercial infrastructure and a network of distributors, our products are sold in 55 countries.**Job Summary**We are seeking a highly skilled Regulatory Affairs Specialist to manage global product...

Job Title: Senior Regulatory Affairs EngineerAbout the Role: We are seeking a highly experienced Senior Regulatory Affairs Engineer to join our team at Com si fos ahir. As a key member of our Corporate Regulatory Affairs Team, you will be responsible for ensuring that our medical devices meet the necessary regulatory requirements for new product development...

Galderma, a leading dermatology company, offers a unique opportunity for a highly skilled Regulatory Affairs Strategist to join its team in Barcelona, Spain. As part of our Global Capability Center, you will be responsible for delivering innovative global regulatory strategies for clinical trial registration with health authorities.About the RoleThis is an...

We are seeking an expert in Regulatory Affairs to join our team at Galderma. This role will focus on preparing and updating the CMC (Chemistry, Manufacturing and Control) dossier sections of assigned products.The ideal candidate will have experience in CMC Regulatory Affairs and a background in the pharmaceutical industry. They will be responsible for...

We are seeking an expert in Regulatory Affairs to join our team at Galderma. As a Regulatory Affairs CMC Specialist, you will be responsible for preparing and updating the CMC dossier sections of assigned products. This includes assessing regulatory impact, reviewing data, and writing/ assembling CMC sections of regulatory submissions.Key responsibilities...

Company Overview: DSM-Firmenich, a leading global provider of innovative products and solutions for the food and pet food industry.Job Description: As a Regulatory Affairs Specialist, you will play a crucial role in ensuring compliance with European regulations and guidelines for our product portfolio. You will work closely with cross-functional teams to...

Job SummaryWe are seeking a highly skilled Senior Packaging Regulatory Affairs Specialist to join our Biopharma Regulatory department at Grifols Sa. This role will be responsible for preparing, reviewing, and following up on documentation generated at the Regulatory Affairs department or needed for a regulatory submission.Key ResponsibilitiesPrepare, review,...

Job Title:Regulatory Affairs SpecialistGalderma Pharma S.A is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a Regulatory Affairs Specialist, you will be responsible for delivering innovative, breakthrough global regulatory strategies for clinical trial registration with health authorities.The ideal candidate will have a strong...

Regulatory Affairs SpecialistAt Ramboll Group A/S, we are seeking a highly skilled Regulatory Affairs Specialist to join our international Health Sciences service line. As a key member of our team, you will be responsible for providing technical support to clients and colleagues on issues relating to product regulatory compliance and stewardship in Spain.Key...

Regulatory Affairs Specialist Job DescriptionSinclair EBD is seeking a skilled Regulatory Affairs Specialist to manage the global product registration and regulatory approvals for our Energy-Based Devices. As a key member of our team, you will ensure compliance with international regulatory authorities and support market entry for EBDs worldwide.About...

About GaldermaWe are a leading dermatology company with a unique legacy and decades of innovation. Our focus is on delivering a science-based portfolio of premium brands and services that meet the needs of consumers and patients.We are looking for a Regulatory Affairs Specialist to join our team. As a CMC expert, you will contribute to the development of...

The Regulatory Affairs department at Werfen is seeking a highly skilled Quality and Regulatory Affairs specialist to join our team in Barcelona, Spain.As a Quality and Regulatory Affairs specialist, you will be responsible for supporting the execution of pre and post-market regulatory affairs departmental functions. This includes assisting in the preparation...

As a Regulatory Affairs Associate Director at Sandoz, you will lead a team of associates within the Regulatory API department, driving and delivering high-quality documentation to support successful submissions. Your responsibilities will include leading, coaching, and mentoring associates, ensuring sufficient training and development opportunities to...

Job OverviewWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Com si fos ahir. The successful candidate will be responsible for ensuring regulatory compliance and ensuring that our medical devices meet the highest standards.About the RoleThe Regulatory Affairs Specialist will be responsible for providing expert knowledge and...

Regulatory Affairs Documentation SpecialistWe are seeking a highly skilled Regulatory Affairs Documentation Specialist to join our Biopharma Regulatory department at Grifols, S.A. This is a fantastic opportunity to work with a global healthcare company that has been improving the health and well-being of people around the world since 1909.Key...