Trabajo de Regulatory Affairs Project Manager en Madrid

Environmental Resources Management (ERM) is seeking an experienced Plant Protection Regulatory Affairs professional to join us as a Project Manager in Southern Europe. This is a great opportunity to join a global consultancy with a strong track record of advising clients in the chemical sector, with a focus on agrochemicals, biocides and REACH, to help them navigate the complexities of the EU...

MFC-2510-344 REGULATORY AFFAIRS MANAGER MADRID Overall responsibilities - To provide regulatory advice and support to the organisation on the content of existing marketing authorisations and for products in development phase. - To provide general regulatory advice and support to other departments. - Review and approval of promotional and non-promotional material to comply with local...

Job Title Regulatory Affairs Data Manager Location Barcelona, Spain (hybrid) Job Description As the Regulatory Affairs Data Manager, you will support regulatory operations by managing, analyzing, and reporting regulatory data. This role involves transitioning from siloed applications to a unified platform, ensuring consistent data management across departments, and executing reporting...

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job...

Job Title: Regulatory Affairs Specialist Spain Full Time Permanent Location: Spain (Madrid) About Novumgen Novumgen is a rapidly expanding, science-driven pharmaceutical company committed to delivering high-quality, accessible medicines across global markets. Our diverse portfolio spans specialty generics, complex formulations, and innovative therapeutic solutions. With a strong focus on...

Regulatory Affairs Study Start Up Specialist II (RASSU) - Prepare, review, and manage regulatory submissions under CTR (Clinical Trials Regulation) using CTIS. - Handle regulatory submissions for medical devices, GMOs, and local country requirements in countries where CTIS is not mandated, including ethics committee submissions. - Prepare and QC Clinical Trial Application forms (via CTIS or...

Regulatory Affairs Study Start Up Specialist II (RASSU) Join to apply for the Regulatory Affairs Study Start Up Specialist II (RASSU) role at CTI Clinical Trial and Consulting Services What You’ll Do - Prepare, review, and manage regulatory submissions under CTR (Clinical Trials Regulation) using CTIS. - Handle regulatory submissions for medical devices, GMOs, and local country requirements in...

When our values align, there's no limit to what we can achieve. Parexel is seeking an experienced Regulatory Affairs Professional to join our dynamic team as a Senior Regulatory Affairs Consultant. This strategic position requires a proactive and agile regulatory professional able to build strategy, drive execution, and address challenges involved in gaining market approvals across international...

A global healthcare leader is seeking an Experienced Regulatory Affairs Professional in Madrid. In this role, you will develop regulatory strategies and support submissions for innovative pharmaceutical products across EMEA. The ideal candidate has a Bachelor’s degree in Life Sciences or Pharmacy and 2+ years of relevant experience. Strong project management and communication skills are...

Regulatory Affairs Specialist – Medical DevicesThe Regulatory Affairs Specialist is responsible for preparing, submitting, and maintaining regulatory documentation to support global approvals of high‑risk or implantable medical devices. This role ensures compliance with U.S. FDA regulations, EU MDR 2017/745, and other international requirements, supporting product lifecycle management from...

Staphyt veille au respect de l'égalité femmes/hommes : Cliquez ici pour télécharger l'index d'égalité femmes/hommes pour Staphyt France At Staphyt, our Regulatory Affairs Division helps clients navigate complex regulatory environments and successfully bring their chemical or biological substances and products to market. We support projects across Plant Protection & Nutrition, Biocides and REACh...

A career at Lombard Odier means working for a renowned global wealth and asset manager, with a strong focus on sustainable investing. An innovative bank of choice for private and institutional clients, our independently owned Firm is one of the best-capitalised banking groups in the world, managing close to CHF 300 billion and operating from over 25 offices across 4 continents. With a history...

Senior Translation Project Manager - Regulatory Submissions page is loaded## Senior Translation Project Manager - Regulatory Submissionslocations: Madrid, Spain: Barcelona, Spain: Reading, Berkshire, United Kingdomtime type: Full timeposted on: Posted Todayjob requisition id: R1519109SENIOR TRANSLATION PROJECT MANAGER – REGULATORY SUBMISSIONS Working with the wider Project Management team, the...

A leading global consulting firm in Madrid is looking for a Senior Project Manager to oversee the administration of REACH consortia. You will manage projects, coordinate activities, and support clients in navigating regulatory compliance. The ideal candidate should have a Master's degree and extensive experience in project management and European chemicals law, particularly REACH. Competitive...

Senior Translation Project Manager – Regulatory Submissions SENIOR TRANSLATION PROJECT MANAGER – REGULATORY SUBMISSIONS Working with the wider Project Management team, the Senior Translation Project Manager – Regulatory Submissions is responsible for coordinating and managing the full lifecycle of Regulatory Submissions for Marketing Authorization translation and localization projects to...

Who we are?Veterinary medicine manufacturersVetpharma is the veterinary division of Chemo, part of the Insud Pharma group, providing Animal Health solutions. We are located in Barcelona, where the group was founded in 1977.In Vetpharma we are a highly qualified team.We have extensive experience in development, registration and marketing veterinary medicinal products, API’s and...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare...

When our values align, there's no limit to what we can achieve. We are seeking a dedicated Regulatory Affairs Labelling professional to join our growing team! This role offers an opportunity to work with global labelling teams, ensuring regulatory compliance and supporting product labelling management across multiple regions. The role can be home or office based in various European...

Company Overview Working for a renowned global wealth and asset manager, with a strong focus on sustainable investing. The firm is one of the best-capitalised banking groups in the world, managing close to CHF 300 billion and operating from over 25 offices across 4 continents. LOCAL COMPLIANCE OFFICER (7-month contract) Reporting to the Chief Compliance Officer Europe, you will be responsible...

When our values align, there's no limit to what we can achieve. About the Role We are seeking an experienced Regulatory Affairs professional to join our team as a European Labelling & Promotional Regulatory Specialist. This key position provides expert guidance across a Therapeutic business unit, delivering both strategic and operational regulatory input to cross-functional teams. The role can...