Trabajo Regulatory Affairs Project Manager en Málaga

1 Year (FREELANCE) Contract Opportunity : EU Regulatory Affairs - Senior Manager (Biotech) A leading biotechnology company is seeking a highly experienced EU Regulatory Affairs Senior Manager to support development-stage projects and initial Marketing Authorisation Applications (MAAs) across Europe. Key Responsibilities : - Lead and support EU Clinical Trial Authorisation (CTA) submissions and...

Regulatory Affairs Manager Crop Protection (f/m/d) Knoell is one of the leading global service providers in regulatory registration, clinical development, and product development support. As a family‑owned business, we take pride in our commitment to the highest standards and believe that people are at the heart of our success. With our team of scientific and regulatory experts and an extensive...

Regulatory Affairs Project Manager Location: Remote/Home Working EU Wide Introduction Our client is seeking a highly skilled and motivated Regulatory Affairs Project Manager to join their dynamic team. This role offers the opportunity to work at the forefront of regulatory science, contributing to the successful registration and market approval of active substances under EU Regulation...

Regulatory Affairs Project Manager Introduction Our client is seeking a highly skilled and motivated Regulatory Affairs Project Manager to join their dynamic team. This role offers the opportunity to work at the forefront of regulatory science, contributing to the successful registration and market approval of active substances under EU Regulation ********* . The ideal candidate will have 5 to 10...

Regulatory Affairs Project Manager Life Cycle Management Get AI-powered advice on this job and more exclusive features. Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries ? PQE Group has been at the forefront of these industries since **** , with 40 subsidiaries and more than **** employees in Europe, Asia and the...

Overview Senior global regulatory role focused on medical devices and combination products (like injector pens and on-body delivery systems). You'll lead regulatory strategy, submissions, and interactions with global authorities - including Notified Bodies, EMA, and FDA. It's a hands-on but strategic position, perfect for someone who knows the medical device regulatory landscape inside out and...

Job Title European Regulatory Affairs Manager Location Hybrid – Munich (Germany), Rome (Italy), Madrid (Spain), Amsterdam (Holland), Prague (Czechia) Remuneration Competitive salary and package, including generous bonus scheme. Overview Regulatory Affairs Manager opportunity working for an established pharmaceutical company that specialises in generic, OTC, and prescription medicines. The...

Local Regulatory Affairs Manager in Spain (Freelance/Part-time) Freelance opportunity in Spain! Join our global team as a Local Regulatory Affairs Manager in Spain. Local Regulatory Affairs Manager will be responsible for ensuring that medicinal and other products comply with applicable regulatory requirements by providing input and coordinating marketing authorization and post-authorization...

Job Title: Regulatory Affairs Manager EuropeLocation: Barcelona, Spain (Onsite)Department: Regulatory/PharmacovigilanceEmployment Type: Full-Time, PermanentIndustry: PharmaceuticalsAbout Vivanta GenericsMSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in **** with a mission to make health care affordable, the company has 17 API and 8 finished...

Overview Join to apply for the Operations Manager (Regulatory Affairs) role at Revolut. About Revolut: People deserve more from their money. More visibility, more control, and more freedom. Since ****, Revolut has been on a mission to deliver just that. Our powerhouse of products—including spending, saving, investing, exchanging, travelling, and more—help our 60+ million customers get more from...

Regulatory Affairs Manager Crop Protection (f/m/d) 2 days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Join Us in Shaping the Future of Regulatory Services. Knoell is one of the leading global service providers in regulatory registration, clinical development, and product development support. As a family-owned business, we take pride in our...

¿Dónde trabajarás? Trabajarás en una destacada compañía farmacéutica italiana con presencia global y una sólida trayectoria de más de 130 años en el sector. Con un equipo de más de 150 profesionales en México. Su enfoque actual abarca áreas clave como riesgo cardiovascular, respiratorio, analgesia, salud sexual masculina y aparato digestivo. Además, están comprometidos con la investigación y el...

In a few words Position: Biotech Senior Project Manager Location: Madrid Experience: +5 years in biotech project management Want to know more? 👇 INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API),...

Empresa especializada en elaboración de productos dietéticos y dietoterápicos, busca incorporar un Responsable de QA y Regulatory con experiencia en laboratorios de suplementación, alimentación, medicamentos y/o bebidas. Su objetivo es liderar los subdepartamentos de QA y Regulatory para garantizar que el producto que se fabrica y se pone en el mercado, sea adecuado/apto/seguro para su uso y...

Regulatory Affairs Specialist – Medical Devices The 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 ********, and other international requirements, supporting product lifecycle management from...

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 Submission Management Prepare, review, and manage regulatory submissions under CTR using CTIS. Handle regulatory submissions for medical devices, GMOs, and local country requirements in countries where CTIS is not...

Avania is hiring for the position of Principal Consultant – EU / UK - Regulatory and Advisory Services . We are seeking an experienced Principal Consultant with expertise in medical device regulatory strategy, especially with the U.S. FDA and EU MDR. This senior role requires strategic insight, hands-on regulatory experience, and the ability to guide medical device companies through complex...

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries ? PQE Group has been at the forefront of these industries since **** , with 40 subsidiaries and more than **** employees in Europe, Asia and the Americas . Due to continued growth, we are seeking an experienced Regulatory Affairs Expert to provide strategic regulatory...

Regulatory Affairs Manager Crop Protection (f/m/d) Knoell is one of the leading global service providers in regulatory registration, clinical development, and product development support. As a family‐owned business, we take pride in our commitment to the highest standards and believe that people are at the heart of our success. With our team of scientific and regulatory experts and an extensive...

Regulatory Affairs Manager Crop Protection (f/m/d) Knoell is one of the leading global service providers in regulatory registration, clinical development, and product development support. As a family‐owned business, we take pride in our commitment to the highest standards and believe that people are at the heart of our success. With our team of scientific and regulatory experts and an extensive...