Safety Pharmacovigilance Lead for Global Sandoz Operations

Há 4 dias


Lisboa, Lisboa, Portugal Sandoz Tempo inteiro

At Sandoz, we're committed to shaping the future of healthcare by providing access to high-quality medicines. As a Safety Pharmacovigilance Lead, you'll play a key role in ensuring the safety of our products and maintaining compliance with international regulations.

The estimated salary for this position is $85,000 - $110,000 per year, depending on location and experience.

We're looking for a highly skilled professional with at least 2 years of experience in pharmacovigilance or drug safety. Your responsibilities will include:

  • Leading pharmacovigilance activities in our affiliate organizations to ensure comprehensive and effective safety procedures;
  • Collaborating closely with local QPPV and regional hubs to maintain awareness of safety profiles and provide expertise;
  • Establishing oversight mechanisms for safety activities outsourced to vendors;
  • Maintaining awareness of national and international regulations for pharmacovigilance;

To be successful in this role, you'll need:

  • A health care sciences background (e.g., Medical Doctor, Nurse, Pharmacist) or equivalent education and experience;
  • Minimum 2 years' experience in drug-safety or pharmacovigilance;
  • Demonstrated leadership and accomplishment in patient safety or similar roles;
  • Knowledge of pharmacological and medical terminology;
  • Good communication, planning, negotiation, organizational, and interpersonal skills;
  • Project management skills;

We offer a dynamic work environment with opportunities for growth and development. Our commitment to diversity and inclusion ensures that our teams reflect the patients and communities we serve. If you're passionate about making a difference in healthcare, join us as a Safety Pharmacovigilance Lead and help shape the future of Sandoz.


  • Patient Safety Specialist

    3 semanas atrás


    Lisboa, Lisboa, Portugal Sandoz Tempo inteiro

    About SandozSandoz is a leading global generic and biosimilar medicines company, with a mission to pioneer access for patients. With a presence in almost 140 countries, our products touch the lives of nearly 500 million patients every year.We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients...


  • Lisboa, Lisboa, Portugal Sandoz Tempo inteiro

    About the Role:We are seeking a highly skilled Patient Safety Expert to lead pharmacovigilance activities in our affiliate in Portugal. The successful candidate will be responsible for ensuring that local safety procedures are comprehensive, effective, compliant, and well embedded in the cross-functional and global-regional-local environment.The ideal...


  • Lisboa, Lisboa, Portugal Sandoz Tempo inteiro

    OverviewSandoz, a leader in the generic and biosimilar medicines industry, seeks a highly skilled Pharmacovigilance Expert Leader to join its team. With a strong focus on patient safety, this role will play a critical part in shaping the future of Sandoz and improving access to low-cost, high-quality medicines for millions of patients worldwide.


  • Lisboa, Lisboa, Portugal Healthcare Businesswomen'S Association Tempo inteiro

    Job Overview: We're seeking a Patient Safety Specialist to lead pharmacovigilance activities in the Sandoz affiliate in Portugal within the context of the Sandoz Pharmacovigilance System, the Sandoz patient safety operating model, and associated quality system.Company Overview: Generic and Biosimilar medicines are the backbone of the global medicines...


  • Lisboa, Lisboa, Portugal Healthcare Businesswomen'S Association Tempo inteiro

    About SandozSandoz, a leading generic and biosimilar medicines company, has the opportunity to shape the future of healthcare. Our innovative production sites, acquisitions, and partnerships enable us to provide low-cost, high-quality medicines sustainably.Why Work at Sandoz?At Sandoz, we value diversity and inclusion. Our agile and collegiate environment...


  • Lisboa, Lisboa, Portugal Phiture Tempo inteiro

    About UsAt Sandoz, we strive to make a meaningful difference in the lives of millions of patients worldwide. Our commitment to innovation and quality has made us a leader in the global medicines industry.We are proud to have touched the lives of almost 500 million patients last year and we're eager to continue our mission of providing low-cost, high-quality...


  • Lisboa, Lisboa, Portugal Phiture Tempo inteiro

    Sandoz, a global leader in generic and biosimilar medicines, is seeking an experienced Patient Safety Leader to join our team. As a key member of our affiliate organization, you will play a crucial role in promoting a thorough understanding of the pharmacovigilance system and ensuring compliance with safety requirements for local activities.We are looking...


  • Lisboa, Lisboa, Portugal PrimeVigilance Tempo inteiro

    Job Overview: PrimeVigilance is seeking a highly skilled Clinical Pharmacovigilance Specialist to join our team in global operations.About the Role: As a key member of our PV team, you will be responsible for reviewing and approving post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials. You...


  • Lisboa, Lisboa, Portugal Organon Tempo inteiro

    **Job Summary**Organon is seeking a highly skilled Drug Safety Specialist to join our team. As a key member of our Pharmacovigilance team, you will be responsible for managing adverse event cases, ensuring compliance with global and local regulations, and providing support for patient safety initiatives.**Key Responsibilities**Manage day-to-day adverse event...


  • Lisboa, Lisboa, Portugal Organón Tempo inteiro

    Job DescriptionCompany OverviewWe are Organón, a company committed to delivering innovative solutions in the field of pharmacovigilance. Our team is dedicated to ensuring the safety of our products and protecting public health.SalaryWe offer a competitive salary ranging from $80,000 to $110,000 per year, depending on experience and qualifications.Job...


  • Lisboa, Lisboa, Portugal Primevigilance Tempo inteiro

    Established in 2008, PrimeVigilance has grown organically year after year to become a leading provider of pharmacovigilance services. As a global company with staff across Europe, North America, and Asia, we cover a range of services including Medical Information, Pharmacovigilance, Regulatory Affairs, and Quality Assurance.We value our relationships with...

  • Medical Safety Professional

    3 semanas atrás


    Lisboa, Lisboa, Portugal Organon Tempo inteiro

    Explore a rewarding career opportunity at Organon, a leading global healthcare company dedicated to improving women's health and well-being.About the RoleWe are seeking an experienced Medical Safety Professional with expertise in pharmacovigilance to join our team. As a key member of our safety organization, you will be responsible for ensuring compliance...


  • Lisboa, Lisboa, Portugal IQVIA Tempo inteiro

    Join IQVIA's International TeamIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.Job DescriptionProvide phone...


  • Lisboa, Lisboa, Portugal Organón Tempo inteiro

    Job DescriptionWe are seeking a highly skilled Pharmaceutical Safety Operations Specialist to join our team at Organón. This role will be based in [Location], and the ideal candidate will have excellent communication skills, both written and verbal.Job SummaryThe Pharmaceutical Safety Operations Specialist will be responsible for managing adverse event...


  • Lisboa, Lisboa, Portugal Organón Tempo inteiro

    Job DescriptionJob Title: Pharmacovigilance SpecialistJob Summary:We are seeking a highly skilled Pharmacovigilance Specialist to join our team at Organon. As a key member of our Pharmacovigilance department, you will be responsible for ensuring the safe and effective use of our products.Responsibilities:Manage adverse event cases from receipt to closure in...


  • Lisboa, Lisboa, Portugal Organon Tempo inteiro

    Job SummaryWe are seeking a highly skilled Pharmacovigilance Specialist to join our team. The ideal candidate will have a strong background in pharmacovigilance and regulatory affairs, with a minimum of 1 year of industry experience.Key ResponsibilitiesManage day-to-day adverse events case intake and follow-up activities in accordance with Global...


  • Lisboa, Lisboa, Portugal Primevigilance Tempo inteiro

    About the Company">We are PrimeVigilance, a leading pharmacovigilance service provider with global reach and expertise. Our team of professionals is dedicated to delivering high-quality support to pharmaceutical and biotechnology partners across various therapy areas.At PrimeVigilance, we prioritize diversity, equity, and inclusion by creating an equal...


  • Lisboa, Lisboa, Portugal Organon Tempo inteiro

    Job DescriptionWe are seeking a highly skilled Pharmacovigilance Specialist to join our team at Organon. The ideal candidate will have a strong background in pharmacovigilance and regulatory affairs, with excellent communication and time management skills.ResponsibilitiesManage day-to-day adverse events case management, including case intake and follow-up...


  • Lisboa, Lisboa, Portugal Organon Tempo inteiro

    About OrganonOrganon is a global healthcare company dedicated to delivering innovative health solutions that empower people to live their best lives. We focus on women's health, biosimilars, and diverse health solutions.Salary InformationThe estimated annual salary for this position is between $65,000 and $90,000, depending on the location and qualifications...


  • Lisboa, Lisboa, Portugal Iqvia Tempo inteiro

    Job SummaryJoin IQVIA's team of medical information specialists and contribute to the development and commercialization of innovative medical treatments.We are seeking a highly skilled Medical Information and Adverse Event Intake Specialist with expertise in Italian and English languages to support our global safety operations team.ResponsibilitiesProvide...