Regulatory Affairs Expert

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...

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...

The Senior Manager, Regulatory Affairs will lead the regional regulatory affairs department at Innovaderm Research, ensuring all services are conducted according to standard operating procedures, applicable regulations, and good clinical practices. Key responsibilities include providing leadership on regulatory activities, planning and assigning work,...

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...

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...

Job OverviewWe are seeking a highly skilled Pharmaceutical Regulatory Expert to join our team at FARMAPROJECTS SAU. This is an exciting opportunity for a professional with a strong background in regulatory affairs to contribute to the success of our organization.

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...

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...

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 Title: Regulatory Affairs CMC SpecialistWe are seeking an experienced Regulatory Affairs CMC Specialist to join our team at Galderma. As a key member of our Regulatory Affairs department, you will be responsible for preparing and updating CMC dossier sections for assigned products.Key Responsibilities:Contribute to global regulatory CMC strategies and...

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...

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...

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...

Company OverviewGalderma is a leading dermatology category leader, operating in approximately 90 countries worldwide. Our innovative, science-based portfolio of premium flagship brands and services spans the full spectrum of the fast-growing dermatology market, including Injectable Aesthetics, Dermo-cosmetics, and Therapeutic Dermatology.We have dedicated...

Farmaprojects SAU is a B2B Pharmaceutical Laboratory company offering a broad portfolio of generic pharmaceutical products and value-added medicines. We are looking for a Regulatory Affairs Senior Specialist to join our Regulatory Affairs Department.Key responsibilities include:Developing assessments and strategic regulatory plans for strategic product...

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...

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...

About ICON plcICON plc is a world-leading healthcare intelligence and clinical research organization that fosters an inclusive environment driving innovation and excellence. We're proud to welcome talented professionals like you to join us on our mission to shape the future of clinical development.Role OverviewWe're seeking a skilled Clinical Trials...

OverviewWerfen is seeking a Regulatory Affairs Specialist to support the execution of pre- and post-market regulatory affairs departmental functions. The ideal candidate will assist in the preparation of documentation and information required to place and keep products on the market, including regulatory submissions, licensing and registrations. Key...