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Johnson & Johnson
Johnson & Johnson
H1B vizos rėmėjasBiotechnologijaFarmacijos produktaiSveikatos priežiūra
Johnson & Johnson yra pasaulinė sveikatos priežiūros bendrovė, veikianti farmacijos, medicinos prietaisų ir vartotojų sveikatos srityse. Jos mokslinių tyrimų ir produktų kūrimo veikla apima onkologijos, imunologijos, neuromokslų bei širdies ir plaučių ligų vaistus ir gydymo būdus, taip pat medicinos technologijų sprendimus širdies ir kraujagyslių priežiūros, ortopedijos, chirurgijos ir regos srityse. Platesnė bendrovės veikla apima ir sveikatos bei gerovės švietimą, plataus masto gamybą, darbą su investuotojais bei pasaulines socialinio poveikio iniciatyvas, sudarančias galimybes dirbti mokslo, klinikinėse, inžinerijos, gamybos, komercinėse ir įmonės funkcijose.
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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.

MXMeksikaHibridinisVisas etatasVyresnysis specialistasPrivaloma Kalba: anglųPrivaloma Kalba: ispanųAnalitikas

Aprašymas

  • 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.

Reikalavimai

  • 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%.

Privalumai

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

Susiję darbai

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