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Dr. Reddy's Laboratories

Global generic medicines and APIs exporter

Senior Regulatory Affairs Analyst

Regulatory & Quality (Life Sciences)Posted on Nov 12
Full-timeSão Paulo, State of São Paulo, BrazilNo salary listed

About the Job

Requirements

  • A completed undergraduate degree in Pharmacy, Pharmaceutical Sciences, Biotechnology, Life Sciences, or a related field.
  • Advanced or fluent English.
  • Eight to ten years of experience in Regulatory Affairs in the pharmaceutical industry.
  • Strong experience with Brazilian regulatory processes and submissions to ANVISA.
  • Experience with new product registrations, product lifecycle management, and post-registration changes.
  • Experience interacting with ANVISA, including technical meetings, responses to requirements, and regulatory appeals.
  • Experience with synthetic medicines, innovative products, biologics, and biosimilars.
  • Consistent knowledge of Brazilian health regulations and ANVISA requirements for drug registration and post-registration.
  • Experience preparing, reviewing, and submitting CTD/eCTD dossiers.
  • Knowledge of GMP/CBPF processes, regulatory inspections, and certification maintenance.
  • Experience managing responses to ANVISA technical requirements.
  • Knowledge of regulatory requirements related to bioequivalence, labeling, package inserts, and electronic submissions.
  • Ability to develop regulatory strategies for new registrations, portfolio expansion, and maintenance of marketed products.
  • Expertise assessing regulatory impacts of manufacturing, quality, supply-chain, and labeling changes.
  • Ability to analyze complex situations, work autonomously, make recommendations, and manage multiple priorities.
  • Ability to build effective relationships with internal and external stakeholders.
  • Strong communication, negotiation, and problem-solving skills, proactivity, and attention to detail.

Responsibilities

  • Conduct regulatory activities for registrations, post-registrations, and portfolio maintenance in Brazil.
  • Participate in defining and implementing regulatory strategies for new registrations, post-registrations, and portfolio expansion.
  • Manage and track registration processes for synthetic medicines, innovative products, biologics, and biosimilars within the assigned portfolio.
  • Coordinate the preparation, review, and submission of CTD/eCTD dossiers.
  • Prepare, review, and track responses to regulatory requirements, administrative appeals, and other ANVISA matters.
  • Participate in and, when applicable, lead technical interactions and meetings with ANVISA related to assigned processes.
  • Conduct and track regulatory activities related to GMP/CBPF and support inspections.
  • Assess and implement post-registration changes and regulatory variations affecting marketed products.
  • Review package inserts, packaging materials, and labeling to ensure regulatory compliance.
  • Act as the regulatory interface for local and international partners, supporting business and licensing initiatives.
  • Monitor regulatory changes and advise internal teams on applicable impacts and requirements.
  • Collaborate with Quality, Research and Development, Supply Chain, Pharmacovigilance, Medical Affairs, and Commercial teams to support regulatory strategies.

Desired Qualifications

  • Postgraduate study and/or a master's degree.
  • Experience in multinational pharmaceutical environments and working with global teams.
  • Experience providing regulatory support for business development, licensing, and strategic partnerships.

About the Company

Dr. Reddy's Laboratories

Global generic medicines and APIs exporter

Dr. Reddy's Laboratories focuses on affordable generic medicines and pharmaceutical ingredients. Its products include generic drugs and active pharmaceutical ingredients (APIs) produced in-house and distributed worldwide. The company grew from a Hyderabad-based startup in 1984, becoming the first Indian firm to export APIs to Europe in 1986 and to enter the U.S. market in the early 1990s, culminating in a 2001 NYSE listing that underscored its global standards. Today, the group operates in over 150 countries, supported by ongoing research and development to create new and improved medications. The core goal is to improve global health by providing high-quality, affordable healthcare solutions at scale.

Company size
10,001+
Company stage
IPO
Headquarters
Hyderabad, India
Founded
1984

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