LogoFresh Jobs Ahead
Johnson & Johnson
Johnson & Johnson
Sponsor pentru viza H1BAsistență medicalăBiotehnologieProduse farmaceutice
Johnson & Johnson este o companie globală din domeniul sănătății, care activează în industria farmaceutică, a dispozitivelor medicale și a produselor pentru sănătatea consumatorilor. Activitățile sale de cercetare și dezvoltare a produselor includ medicamente și terapii pentru oncologie, imunologie, neuroștiință și afecțiuni cardiopulmonare, precum și soluții MedTech pentru îngrijirea cardiovasculară, ortopedie, chirurgie și oftalmologie. Activitatea mai amplă a companiei include, de asemenea, educație pentru sănătate și bunăstare, producție la scară largă, activități pentru investitori și inițiative globale cu impact social, oferind oportunități în domenii științifice, clinice, inginerești, de producție, comerciale și corporative.
LinkedIn
Locurile de muncă ale companiei

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.

MXMexicHibridNormă întreagăSeniorLimbă Obligatorie: englezăLimbă Obligatorie: spaniolăAnalist

Descriere

  • 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.

Cerințe

  • 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%.

Beneficii

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

Locuri de muncă similare

General Motors

Senior Embedded Software Engineer, General Motors

General Motors
Sponsor pentru viza H1BIndustria autoIndustria prelucrătoareTransport
USStatele Unite ale AmericiiMIMichiganHibridNormă întreagăSeniorLimbă Obligatorie: englezăInginer full-stackInginer software
Securitate cibernetică

Develop embedded C and AUTOSAR controls software for General Motors, leading delivery across the software lifecycle. Test, debug, and improve supplier solutions in a hybrid role based in Milford, Michigan.

Deschide