Regulatory Affairs Professional

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.

About Solutia Life SciencesSolutia Life Sciences is a recruitment division of Solutia, specializing in technical and middle management profiles in the pharmaceutical, biotech, and medical device sectors.We are currently selecting a Regulatory Affairs Technician for a pharmaceutical company focused on developing and producing innovative oncology products and...

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,...

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...

About the RoleWe are seeking a talented Regulatory Affairs Specialist to join our R&D team in Barcelona. As a key member of our team, you will be responsible for preparing documentation, maintaining product information files (PIFs), and managing technical dossiers for product registration in European markets.Key ResponsibilitiesPrepare and maintain PIFs and...

Job Title: Senior Regulatory Affairs EngineerJob Summary:We are seeking a highly skilled Senior Regulatory Affairs Engineer to join our Corporate Regulatory Affairs Team. The successful candidate will be responsible for ensuring regulatory requirements are met for new product development and design changes to established legacy devices.Key Responsibilities:*...

Job DescriptionWe are seeking a highly skilled Regulatory Affairs Consultant to join our Clinical and Regulatory Team at Clarivate. As a key member of our team, you will be responsible for delivering high-quality regulatory services to our global clients.Key Responsibilities:Project Delivery Support: Act as a point of contact for customers throughout a...

Job Title: Regulatory Affairs SpecialistAt Galderma, we are 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. You will work closely with our global...

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...

Job OverviewRegulatory Affairs Leader at WerfenJob Function: QA&RAAbout the PositionThis role provides regulatory support for manufactured products and customer products. The successful candidate will prepare and submit documentation according to legislation for different countries.Key Responsibilities:Implement new regulatory...

Job SummaryThe Senior Manager, Regulatory Affairs will lead the regional regulatory affairs department to ensure compliance with Innovaderm's standard operating procedures, applicable regulations, and good clinical practices. Key responsibilities include providing strategic guidance on regulatory activities, overseeing the performance of direct reports, and...

Job Details: At Ablecloset, we are seeking a highly skilled Senior Regulatory Affairs Engineer to join our Corporate Regulatory Affairs Team. The Role: This position is responsible for ensuring regulatory requirements are met for new product development and design changes to established legacy devices. The successful candidate will work closely with Research...

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...

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...

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...

Galderma Pharma S.A. is a dermatology category leader with a unique legacy and decades of innovation, present in approximately 90 countries worldwide. Our science-based portfolio spans the full spectrum of the fast-growing dermatology market through Injectables, Dermo-cosmetics, and Therapeutic Dermatology. We are seeking a highly motivated and...

About The Zonal GroupWe are a global medical aesthetics organization that delivers 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 OverviewThe Regulatory Affairs Specialist will be responsible for...

Job Summary:At Vetpharma, we are seeking a highly skilled Regulatory Affairs Associate to join our team. The successful candidate will be responsible for compiling and managing registration dossiers and coordinating submissions to health authorities until product approval and launch.Key Responsibilities:• Compile and manage registration dossiers and...

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...

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...