Pharmacovigilance Manager US & Latam

Tata Consultancy Services

São Paulo

Presencial

BRL 80 000 - 120 000

Tempo integral

14 dias+

Uma candidatura completa num minuto

Currículo e carta de apresentação personalizados, prontos a enviar.

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Vantagens oferecidas por esta oferta de emprego

Health and life insurance
Gympass
Support programs including psychological, legal, social, and financial assistance
Partnerships with educational and training institutions
Reimbursement for certifications
Access to TCS Learning Portal
International experience opportunities
Referral bonuses and recognition programs

Resumo da oferta

A leading IT services company seeks a Pharmacovigilance Manager for US & Latam. This role involves managing safety projects, ensuring compliance with FDA regulations, and collaborating with stakeholders. Ideal candidates will have extensive experience in pharma/biotech and strong communication skills. Join a culture of continuous learning and growth.

Qualificações

  • At least 10 years of experience in pharma/biotech, with 6 years in US FDA regulations and project management.
  • Experience in team management and understanding of business principles.

Responsabilidades

  • Maintain a comprehensive understanding of FDA and regional regulations.
  • Support the US Local safety team by managing projects and communicating effectively.
  • Ensure adherence to processes and maintain relevant documentation.

Conhecimentos

Attention to Detail
Communication

Formação académica

University degree in Life Sciences or Pharmacy

Descrição da oferta de emprego

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Come to one of the biggest IT Services companies in the world! Here you can transform your career!

Why join TCS? We believe that people make the difference, which is why we foster a culture of continuous learning, opportunities for growth, and mutual development. It's an ideal environment to expand ideas with the right tools, contributing to our collective success.

We are looking for a Pharmacovigilance Manager for US & Latam who is eager to learn and advance their career.

In this role, you will:

  • Maintain a comprehensive understanding of FDA and regional regulations;
  • Support the US Local safety team by initiating, planning, executing, controlling, and closing projects, and communicate procedures and solutions effectively under tight deadlines;
  • Engage regularly with internal and external stakeholders through proper channels to ensure accuracy, completeness, and issue resolution;
  • Ensure adherence to processes, and maintain relevant documentation;
  • Assess the impact of changes on safety requirements and coordinate with stakeholders for timely decisions;
  • Escalate unresolved issues following the established process;
  • Meet quality and turnaround time targets consistently;
  • Collaborate across functions to ensure smooth communication and delivery.

Preferred qualifications:

  • Strong attention to detail and excellent communication skills in English (verbal & written);
  • Experience in team management and understanding of business principles;
  • University degree in Life Sciences or Pharmacy;
  • At least 10 years of experience in pharma/biotech, with 6 years in US FDA regulations and project management;
  • Personal initiative, responsibility, flexibility, and ability to handle multiple projects independently.

Application instructions:

Please attach your resume in English.

What we offer:

  • Health and life insurance
  • Gympass
  • Support programs including psychological, legal, social, and financial assistance
  • Partnerships with educational and training institutions
  • Reimbursement for certifications
  • Access to TCS Learning Portal
  • International experience opportunities
  • Referral bonuses and recognition programs

Tata Consultancy Services is an equal opportunity employer committed to diversity and inclusion. We welcome candidates from all backgrounds and encourage participation in our recruitment process.

Join us and be part of an inclusive culture that respects individuality and promotes equity across gender, disability, LGBTQIA+, religion, race, and ethnicity.

Additional details
  • Seniority level: Mid-Senior level
  • Employment type: Full-time
  • Job function: Management
  • Industry: Pharmaceutical Manufacturing
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