Regulatory Compliance Specialist for Global Medical Devices

hace 1 día


Valencia, Valencia, España Edwards Lifesciences A tiempo completo
Job Description

At Edwards Lifesciences, we're driven by a passion to improve patient lives. As a global leader in structural heart innovation, we offer rewarding opportunities and exciting challenges in a dynamic and friendly work environment.

About the Role

This is a unique career opportunity for an Associate Specialist, Quality Compliance role in Spain-Valencia. You'll bring your expertise and passion for problem-solving to partner with various teams to influence decision-making for a product's entire lifecycle.

Your key responsibilities will include:

  • Fulfilling applicable medical device regulations, including ISO13485 and other relevant requirements for designated complaint handling units.
  • Evaluating events for reportability to competent authorities.
  • Investigating complaints with the support of higher-level team members or managers.
What We're Looking For

We need someone with:

  • A Bachelor's Degree in a related field.
  • 1 year experience in complaint handling or similar roles.
  • Experience working in a medical device (cardiovascular, endovascular, or other critical care/surgical products), healthcare, or a related environment.
Benefits and Work Environment

We offer a competitive compensation package, flexible working hours, remote working options, pension plan, life insurance, medical plan, meal vouchers, service awards, enhanced leave benefits, employee stock purchase programme, employee assistance programme, comprehensive wellness programme, and much more.

Join Our Team

At Edwards Lifesciences, we foster a diverse and inclusive work environment where all employees can grow, personally and professionally. We offer on-the-job development, training opportunities, and the support and guidance provided by dedicated employee groups.



  • Valencia, Valencia, España Edwards Lifesciences Gruppe A tiempo completo

    About the RoleWe are seeking a highly skilled and experienced Senior Compliance Specialist to join our team in Valencia, Spain. As a key member of our quality compliance department, you will play a critical role in ensuring that our medical devices meet the highest standards of regulatory requirements.Key ResponsibilitiesEvaluate complaints and determine if...


  • Valencia, Valencia, España Edwards Lifesciences A tiempo completo

    Innovation at Edwards Lifesciences drives improvements in patient lives worldwide. As a key player in the development of groundbreaking technologies, you will be part of a global team shaping medical innovation.About UsWe are a leading structural heart innovation company committed to improving patient outcomes and discovering lasting solutions for unmet...


  • Valencia, Valencia, España ADM A tiempo completo

    About the RoleWe are seeking a skilled Regulatory Affairs Specialist to join our team at ADM. This role will be responsible for ensuring global compliance with regulatory requirements for our Human and Wellness (H&W) portfolio.ResponsibilitiesLeverage your knowledge of global regulatory compliance to own assessments of permissibility and suitability in the...


  • Valencia, Valencia, España ADM A tiempo completo

    At ADM, we seek a skilled Regulatory Compliance Specialist to join our team.Job OverviewThis role involves leveraging global regulatory compliance of the Human & Welfare portfolio by owning assessments of permissibility and suitability in the UK, EU, and US. The ideal candidate will coordinate these assessments with regional SMEs outside the EU to unlock key...


  • Valencia, Valencia, España Edwards Lifesciences A tiempo completo

    At Edwards Lifesciences, innovation is driven by a passion to improve patient lives. As a leading global structural heart innovation company, we serve millions of patients in over 100 countries.About the RoleThis exciting career opportunity as Associate Specialist, Quality Compliance offers a unique chance to contribute meaningfully to patient outcomes and...


  • Valencia, Valencia, España ADM A tiempo completo

    Job OverviewWe are seeking a highly skilled Regulatory Compliance Specialist to join our team at ADM. This is a fantastic opportunity to leverage your expertise in regulatory affairs and compliance to drive business growth and success.


  • Valencia, Valencia, España ADM A tiempo completo

    About the RoleThe Regulatory Compliance Specialist will be responsible for ensuring global regulatory compliance of the H&W portfolio by owning assessments of permissibility and suitability in UK, EU, and US, and coordinating assessments with regional SMEs outside the EU to unlock key markets according to the commercial strategy.This role involves leveraging...

  • Document Specialist I

    hace 2 meses


    Valencia, Valencia, España Gaming Laboratories International A tiempo completo

    Job Title: Document Specialist I - Regulatory Compliance ExpertAbout Us: Gaming Laboratories International (GLI) is a global leader in the testing and certification of gaming devices and systems, with over 30 years of experience in the industry.Job Summary: We are seeking a Document Specialist I to support our QA team in reviewing engineering test files for...


  • Valencia, Valencia, España ADM A tiempo completo

    About the RoleWe are seeking a skilled Global Regulatory Affairs Specialist to join our team at ADM Denmark.Job Description:The Senior Regulatory Affairs Associate owns/leverages the registrations, renewals and variations of the products in the market and works in conjunction with the RSA Strategy and Development team to assess and ensure timely and accurate...


  • Valencia, Valencia, España ADM A tiempo completo

    Unlock Your Potential with ADMWe are seeking a highly skilled and motivated Senior Regulatory Affairs Specialist to join our team in Denmark. As a key member of our Regulatory Affairs team, you will play a crucial role in ensuring the compliance of our human and animal nutrition products with EU and international regulations.About the RoleThe Senior...


  • Valencia, Valencia, España Gaming Laboratories International A tiempo completo

    At Gaming Laboratories International, we are the global leader in testing and certification of gaming devices and systems. We have over 33 years of experience in providing technical consulting services to regulators, manufacturers, and engineering staff.We are seeking a Senior Gaming Compliance Specialist to provide technical consulting services to...


  • Valencia, Valencia, España Edwards Lifesciences A tiempo completo

    At Edwards Lifesciences, we are committed to improving patient lives through innovative medical technologies. We are currently seeking a Quality Compliance Specialist to join our team in Spain.Job OverviewThis is a unique opportunity to make a meaningful contribution to the development of groundbreaking technologies while ensuring compliance with regulatory...


  • Valencia, Valencia, España Adm A tiempo completo

    About ADMAt ADM, we're a global leader in health and wellness through cutting-edge ingredient solutions for humans and animals. Our portfolio includes prebiotics, botanicals, plant-based oils, and microbiome solutions.About the RoleWe're seeking a Regulatory Affairs Manager to drive compliance, open new markets, and ensure our innovative products meet EU/UK...


  • Valencia, Valencia, España Analog Devices A tiempo completo

    Job OverviewAnalog Devices, a global leader in semiconductor innovation, is seeking a highly skilled Senior Verification Specialist to join its esteemed team. With a strong focus on delivering breakthroughs at the Intelligent Edge, Analog Devices combines analog, digital, and software technologies to drive advancements in digitized factories, mobility, and...


  • Valencia, Valencia, España Analog Devices, Inc. A tiempo completo

    Company OverviewAnalog Devices, Inc. is a global semiconductor leader that bridges the physical and digital worlds to enable breakthroughs at the Intelligent Edge. Our company focuses on employees through beneficial programs, aligned goals, continuous learning opportunities, and practices that create a more sustainable future.Job SummaryWe are seeking a...


  • Valencia, Valencia, España Adm A tiempo completo

    Job Title: Regulatory Affairs ManagerAbout the Role:At ADM, we're dedicated to improving global health and wellness through cutting-edge ingredient solutions for both humans and animals. As a Regulatory Affairs Manager, you will be responsible for ensuring our innovative products meet EU/UK regulatory standards.Your Responsibilities:Conduct gap analyses to...


  • Valencia, Valencia, España Analog Devices A tiempo completo

    We are seeking an energetic signal processing/ML engineer to couple ADI's advanced technologies to the physiological challenges in the market. The candidate will develop and test digital signal processing techniques and algorithms for medical devices, including vital signs monitoring and bioimpedance.Responsibilities:Develop and test digital signal...


  • Valencia, Valencia, España Edwards Lifesciences A tiempo completo

    Job OverviewWe are seeking a skilled Senior Quality Compliance Specialist to join our team at Edwards Lifesciences. As a key member of our quality team, you will play a crucial role in ensuring the highest standards of integrity and safety in our product development process.About UsEdwards Lifesciences is a global leader in structural heart innovation,...


  • Valencia, Valencia, España RingCentral A tiempo completo

    About the RoleRingCentral is a leading provider of business cloud communications and contact center solutions. We are seeking a highly skilled Risk and Compliance Specialist to join our team in Valencia, Spain.Job DescriptionWe are looking for a proactive problem-solver with excellent communication skills and a strong understanding of governance, risk, and...


  • Valencia, Valencia, España Edwards Lifesciences A tiempo completo

    Fulfilling medical device regulations in Spain is a vital role at Edwards Lifesciences. This position requires expertise in ISO13485 and other applicable requirements for complaint handling units, as well as event evaluation for reportability to regulatory bodies.