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Johnson & Johnson
Johnson & Johnson
Sponzor vizuma H1BBiotehnologijaFarmacevtski izdelkiZdravstveno varstvo
Johnson & Johnson je globalno zdravstveno podjetje, ki deluje na področju farmacevtskih izdelkov, medicinskih pripomočkov in potrošniškega zdravja. Njegove raziskovalne in razvojne dejavnosti vključujejo zdravila in terapije za onkologijo, imunologijo, nevroznanost in kardiopulmonalne bolezni ter rešitve MedTech za kardiovaskularno oskrbo, ortopedijo, kirurgijo in oftalmologijo. Širše delo podjetja vključuje tudi izobraževanje o zdravju in dobrem počutju, obsežno proizvodnjo, dejavnosti za vlagatelje ter globalne pobude z družbenim učinkom, kar ustvarja priložnosti na znanstvenih, kliničnih, inženirskih, proizvodnih, komercialnih in korporativnih področjih.
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Delovna mesta v podjetju

Senior Techno-Vigilance Analyst – Johnson & Johnson, Hybrid in Mexico City

Oversee drug and medical device safety monitoring at Johnson & Johnson, investigating signals and root causes. Improve safety processes and help manage product risks across development, clinical trials, and regulatory approval.

MXMehikaHibridnoPolni delovni časSeniorZahtevani Jezik: angleščinaZahtevani Jezik: španščinaAnalitik

Opis

  • Investigate safety signals, analyze root causes, and conduct safety monitoring.
  • Monitor drug and medical device safety and complete follow-up under established standards and protocols.
  • Prepare and present reports based on customers’ use of company products.
  • Apply risk-based systems to identify, assess, and manage techno-vigilance and pharmacovigilance requirements.
  • Review safety data and signals throughout ongoing monitoring activities.
  • Recommend improvements to department processes and systems.
  • Address external stakeholders’ questions about product information and developments.
  • Train junior colleagues in relevant techniques, processes, and responsibilities.
  • Work across disciplines to manage and reduce safety risks from product development through clinical trials and regulatory approval.

Zahteve

  • Degree-level education in chemistry, medicine, pharmacy (QFB), or biomedical engineering.
  • At least three years of pharmacovigilance and techno-vigilance experience.
  • Skills in process optimization and quality management systems (QMS).
  • Experience reporting serious adverse events, writing reports, health intelligence, and safety orientation.
  • Root cause analysis (RCA) skills.
  • Knowledge of clinical operations, regulatory affairs management, pharmacovigilance, performance measurement, critical thinking, and safety investigations.
  • Spanish proficiency is required.
  • English proficiency is preferred.
  • Limited domestic or international travel may be required, generally under 10%.

Ugodnosti

  • An inclusive work environment.
  • Equal employment opportunity.
  • Interview accommodations for applicants with disabilities.
  • Limited domestic or international travel, generally under 10%.

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