Post Market Quality and Regulatory Professionals
hace 6 meses
Vous souhaitez donner du sens à votre métier ?
Vous voulez contribuer à l'amélioration de nos soins de santé ?
Alors rejoignez notre équipe
Your Challenge:
- Embedded in the fast growing global Quality and Regulatory Team, you ensure regulatory compliance of our post market activities, managing our Health IT software medical devices.
- You review post market risk assessments performed by the clinical teams and assess the related product issues for reportability.
- Supporting the international Product Quality teams you drive and guide the cross functional teams addressing product issues to initiate, define and implement effective preventive and corrective actions.
- You drive and ensure compliant and timely resolution of vigilance related tasks like incident and trend reporting, field safety corrective actions for all applicable regulatory agencies.
- You conduct Post Market Surveillance activities and prepare and approve formal written reports, expressing opinions on the adequacy and effectiveness of the system and activity reviewed.
- You ensure that customer and service communication is regulatory compliant and accurate Your regular trend analysis reporting on product quality in our customer base supports senior management in taking effective decision for quality improvements.
- In our fast-growing business segment, your regulatory consulting is key in continuous improvement of our business processes.
Your Profile:
- University Degree (Engineering, Computer Science or Science) or equivalent from experience
- Minimum 3-5 years’ experience in a regulated industry - preferably medical device or related - in project management, analyst, technical support, quality management, or quality assurance and regulatory affairs position
- Familiar with international regulations and standards pertaining to medical devices development and servicing; familiarity with ISO 9001, ISO 13485, ISO 14971, MDR and ability to interpret and work with regulations and standards
- Active experience in Authority Communication of incidents and field safety corrective actions.
- Exposure to risk management processes, CAPA, Vigilance Management, Post Market Surveillance and software development Team player with self-starter attitude and excellent communication, collaboration, negotiation, conflict resolution, relationship-building skills
- Strong organizational skills, the ability to meet deadlines and the ability to navigate in an environment with several quality management systems.
- Experience with regulatory requirements for After Sales Processes and writing process documentation.
- Knowledge of data analysis and statistical techniques, knowledge of R programming language is an asset.
- Very good English verbal and written language skills, knowledge of one of the following languages German, French, Italian or Dutch is an asset.
- This position offers stepwise growth with adaptive challenges based on your experiences, so junior, senior and professionals profiles are welcome
Our benefits for you:
- A major challenge in an exciting, innovative and international high-tech company
- A permanent employment contract for long-term perspective
- A competitive salary package complemented by fringe benefits
- Flexible working time, adapting to the personal needs and preferences
-
Director, Quality and Regulatory
hace 2 semanas
España Thermo Fisher Scientific A tiempo completoThermo Fisher Scientific - Barcelona, SpainNegotiableFull-Time1 positionWhen you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your...
-
Regulatory Manager
hace 4 días
España Parexel International A tiempo completoAre you an experienced regulatory professional looking for a new opportunity? We are currently seeking a talented CMC Regulatory Manager (Regulatory Affairs Consultant) to join our dynamic team! This is a client dedicated project, and the role can be office or home based in various European locations.As the CMC Regulatory Manager, you will play a vital role...
-
Regulatory Manager
hace 1 mes
España Parexel A tiempo completoWhen our values align, there's no limit to what we can achieve. Are you an experienced regulatory professional looking for a new opportunity? We are currently seeking a talented CMC Regulatory Manager (Regulatory Affairs Consultant) to join our dynamic team! This is a client dedicated project, and the role can be office or home based in various European...
-
Senior Regulatory Affairs Engineer
hace 1 mes
España AbleCloset A tiempo completoJob Details: Senior Regulatory Affairs Engineer (Pre-Market)Full details of the job.Vacancy Name: Senior Regulatory Affairs Engineer (Pre-Market)Vacancy No: VN179Employment Type: Full-TimeLocation: Esplugues del Llobregat (Barcelona)The RoleSinclair is currently looking for a Pre-Market Regulatory Affairs Engineer at its offices located in Esplugues del...
-
Technical Manager Post-market Quality
hace 1 mes
España Grifols SA A tiempo completo¿Te gustaría unirte a un equipo internacional que trabaja para mejorar el futuro del sector de la salud? ¿Quieres contribuir a mejorar la vida de millones de personas? Grifols es una compañía global del sector de la salud que desde 1909 mejora la salud y el bienestar de las personas en todo el mundo. Somos líderes en medicamentos hemoderivados y...
-
Associate Director, Regulatory Affairs
hace 1 mes
España Cpl Healthcare A tiempo completoJob Title: Associate Director, Regulatory Affairs - Medical Device/Post-Market SurveillanceJob Type: Full Time, Permanent PositionLocation: Spain, Madrid – HybridRemuneration: Attractive salary and packageAn exciting opportunity to join a growing pharmaceutical company that specializes in Cancer and Supportive Care, Gastroenterology, and Hepatology. Due to...
-
España Babel Profiles S.L A tiempo completoAre you passionate about leading continuous improvement in quality systems and ensuring products meet the highest regulatory standards? Do you consider yourself an expert in ISO 9001, ISO 14001, or other international regulations and want to make a difference in a global company? Are you ready to drive quality culture at all levels of an organization and...
-
España Babel Profiles S.L A tiempo completoAre you passionate about leading continuous improvement in quality systems and ensuring products meet the highest regulatory standards? Do you consider yourself an expert in ISO 9001, ISO 14001, or other international regulations and want to make a difference in a global company? Are you ready to drive quality culture at all levels of an organization and...
-
Regulatory And Quality Expert
hace 2 semanas
España buscojobs España A tiempo completoDesde IMAN Temporing, empresa especializada en RRHH, queremos acompañarte en tu trayectoria laboral.#ConectamoseltalentoconlasoportunidadesDesde IMAN TEMPORING TARRAGONA nos encontramos en búsqueda de un / a REGULATORY AND QUALITY EXPERT para una empresa ubicada en Vila-Seca.¿Cuáles serán tus funciones?Notificación de productos (Generalitat, Código...
-
Quality Assurance
hace 1 mes
España Ferring Pharmaceuticals, Inc. A tiempo completoJob Description: At Ferring Pharmaceuticals, we help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused on scientific advances in the areas of reproductive and women’s health, gastroenterology, and urology. Ferring + You is all about working together and sharing ideas, so that we...
-
Quality Assurance
hace 1 mes
España Ferring Pharmaceuticals, Inc. A tiempo completoJob Description: At Ferring Pharmaceuticals, we help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused on scientific advances in the areas of reproductive and women’s health, gastroenterology, and urology. Ferring + You is all about working together and sharing ideas, so that we...
-
Quality Assurance
hace 1 mes
España Ferring Pharmaceuticals A tiempo completoJob Description: At Ferring Pharmaceuticals, we help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused on scientific advances in the areas of reproductive and women’s health, gastroenterology, and urology. Ferring + You is all about working together and sharing ideas, so that we...
-
Global Quality Regulatory API Specialist
hace 4 semanas
España Insud Pharma A tiempo completoWho we are? Today, we are a pharmaceutical group with a track record spanning over 45 years and a footprint in more than 50 countries, led by Leandro and Lucas Sigman. Our overarching goal is to improve people's health all over the world, providing accessible, effective, safe, quality medicines through our various business units, underpinned by continuous...
-
España Roche A tiempo completoThe Position Who We Are At Roche, we are passionate about transforming patients’ lives and we are fearless in both decision and action - we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. We do this today to build...
-
Quality Assurance
hace 1 mes
España Ferring Pharmaceuticals A tiempo completoQuality Assurance & Regulatory Affairs Specialist - Maternity leave coverJob Description:At Ferring Pharmaceuticals, we help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused on scientific advances in the areas of reproductive and women's health, gastroenterology, and urology....
-
Regulatory Affairs Manager
hace 1 mes
España AstraZeneca GmbH A tiempo completoRegulatory Affairs ManagerLocation: London St PancrasCompetitive salary, bonus & benefitsJoin our Biopharmaceuticals Business Unit as a Regulatory Affairs Manager and play a pivotal role in identifying regulatory strategies to support commercial and business objectives. This role offers the opportunity to plan and execute workload for defined product...
-
Regulatory Compliance specialist or Manager
hace 4 semanas
España Merlin Digital Partner A tiempo completoWe are Merlin Digital Partner, a leading IT and Digital headhunting company with over a decade of experience. We've successfully collaborated with industry heavyweights such as Wallapop, Glovo, Banc Sabadell, and Factorial. Our emphasis lies in people-centric approaches and optimizing selection processes. Our mission is to revolutionize companies by...
-
Sr. Manager, Post Marketing Study
hace 3 semanas
España Argenx A tiempo completo(Sr) Manager Post-Marketing Requirement Studies (PMR) Accountable for the operational activities including the planning, conducting, and completing argenx post-marketing studies globally (excluding Japan) in compliance with regulatory requirements. Plan, coordinate, and manage the selection and operations of CROs and other study vendors. ROLE...
-
Regulatory Affairs Specialist- EBD
hace 1 mes
España The Zonal Group A tiempo completoJob Details: Regulatory Affairs Specialist- EBDFull details of the job. Vacancy Name Vacancy Name Regulatory Affairs Specialist- EBD Vacancy No Vacancy No VN309 Employment Type Employment Type Full-Time Location About the JobSinclair is looking for a Regulatory Affairs Specialist to manage the global product...
-
Regulatory Affairs Associate
hace 1 mes
España Galderma Pharma S.A A tiempo completoRegulatory Affairs Associate With a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that spans the full spectrum of the fast-growing dermatology...