D

Dr. Reddy's Laboratories

Global generic medicines and APIs exporter

Head of Medical Affairs

Biology & BiotechConfirmed live in the last 24 hours
Full-timePrinceton, NJ, USANo salary listedIn-person

About the Job

Requirements

  • MD, DO, PharmD, or PhD is required.
  • At least 15 years of progressive pharmaceutical or biopharmaceutical experience, including 5–10 years in Medical Affairs leadership.
  • Therapeutic expertise in Oncology, Immunology/Rheumatology, Rare Disease, or Neurology.
  • Strong knowledge of FDA regulatory pathways, promotional compliance, health economics and outcomes research (HEOR), and real-world evidence.
  • Commitment to compliance, ethics, and patient-centered decision making.

Responsibilities

  • Define and execute the North America Medical Affairs strategy across biosimilars, biologics, specialty products, generics, and complex generics.
  • Serve as the senior medical authority for North America products and pipeline assets.
  • Lead medical launch readiness, evidence generation, publication planning, and scientific communications.
  • Provide scientific input on portfolio selection, development programs, and regulatory interactions, including therapeutic equivalence, biosimilarity, and interchangeability.
  • Oversee real-world evidence, HEOR, investigator-sponsored studies, and post-marketing research.
  • Build the key opinion leader (KOL) engagement strategy, lead advisory boards, and represent the organization at major scientific conferences.
  • Run advisory boards, scientific exchange programs, and expert consultations to shape development and commercial strategy.
  • Scope, build, and lead a high-performing team including medical science liaisons (MSLs), HEOR, Scientific Communications, and Medical Information.
  • Partner with Commercial and Market Access on payer value propositions and participate in promotional and Legal-Medical-Regulatory reviews.
  • Lead medical due diligence for licensing, acquisition, and portfolio expansion opportunities.
  • Assess clinical differentiation, unmet needs, competitive landscapes, and evidence needs for potential new assets.
  • Ensure compliance with FDA regulations, the PhRMA Code, OIG guidance, and internal SOPs and governance standards.
  • Work with Pharmacovigilance and Quality on medical review of safety and product-related matters.
  • Establish and maintain Medical Affairs SOPs, governance processes, and quality standards.

Desired Qualifications

  • Board certification or post-doctoral clinical training is preferred.
  • Experience across biosimilars, biologics, and small-molecule or complex generics is strongly preferred.
  • Proven success leading Medical Affairs for product launches and building field medical teams.
  • Prior Medical Affairs experience at both large and smaller pharmaceutical organizations is ideal.

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

Recently Posted Jobs

Explore more opportunities at Dr. Reddy's Laboratories

See more jobs