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Johnson & Johnson
Johnson & Johnson
Sponzor vizuma H1BFarmacevtski izdelkiZdravstveno varstvoZdravstveno zavarovanje
Johnson & Johnson je globalno zdravstveno podjetje, ki deluje na področju inovativne medicine in medicinske tehnologije. Njegove ekipe razvijajo rešitve na področjih onkologije, imunologije, nevroznanosti, specializirane oftalmologije, interventne oskrbe in ortopedije ter združujejo znanost in tehnologijo za reševanje kompleksnih zdravstvenih potreb. Podjetje poudarja tudi enakost na področju zdravja, okoljsko trajnost, raznolikost in vključevanje pri oskrbi zdravstvenih delavcev, pacientov in skupnosti po vsem svetu.
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Delovna mesta v podjetju

Senior Techno-Vigilance Analyst

Lead safety monitoring, signal assessment, and investigations for Johnson & Johnson products. Support risk controls, reporting, and quality system improvements.

MXMehikaHibridnoPolni delovni časSeniorZahtevani Jezik: angleščinaZahtevani Jezik: španščinaAnalitik

Opis

  • Investigate safety signals through root cause analysis and monitoring to identify, assess, and manage risks.
  • Monitor medical device and drug safety and conduct follow-up in line with organizational standards and protocols.
  • Prepare and present reports based on customers’ use of company products.
  • Apply risk-based systems independently to identify, assess, and manage techno-vigilance and pharmacovigilance requirements.
  • Assess safety data and signals as part of ongoing techno-vigilance and pharmacovigilance activities.
  • Recommend improvements to department processes and systems.
  • Address external stakeholder questions about product information and developments.
  • Train less experienced colleagues in relevant techniques, processes, and responsibilities.
  • Work across disciplines to manage and reduce safety risks through product development, clinical trials, and regulatory approval.

Zahteve

  • Degree in chemistry, medicine, pharmacy (QFB), or biomedical engineering.
  • At least three years of experience in pharmacovigilance and techno-vigilance activities.
  • Skills in process optimization and quality management systems (QMS).
  • Experience with serious adverse event reporting, report writing, 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 language skills required.
  • English proficiency preferred.
  • Willingness to travel domestically or internationally as needed, generally less than 10%.

Ugodnosti

  • Inclusive work environment.
  • Equal opportunity employment.
  • Interview accommodations for applicants with disabilities.
  • Domestic or international travel may be required, generally less than 10%.

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