Dr. Reddy’s Laboratories: Head, Medical Affairs — Princeton, NJ, United States

Dr. Reddy’s Laboratories lists a Head, Medical Affairs opening in Princeton, NJ, United States. The position is listed as full-time. The job description covers pharmacovigilance, regulatory affairs, pharmacy, compliance, business development, marketing, communication.

Recruitment overview

OrganisationDr. Reddy’s Laboratories
Post / roleHead, Medical Affairs
Employment typeFull-time
Notification / job IDREF29751E
Job locationPrinceton, NJ, United States
Work arrangementOn-site
Educational qualificationQualification references: PhD / doctorate
Experience required15+ years of progressive pharmaceutical/biopharmaceutical experience, including 5–10 years in Medical Affairs leadership
Salary / stipendSee employer notice for pay details
Last date to applySee official notice

About Dr. Reddy’s Laboratories

Dr. Reddy’s Laboratories is a pharmaceutical business with research and development, medicine-manufacturing and commercial activities. Its employer description centres on making affordable and innovative medicines accessible. The organisation connects scientific development with the production and delivery of pharmaceutical products, rather than operating only as a research laboratory. Its published business priorities include strengthening existing medicine activities, developing future opportunities and conducting operations with attention to people, resources and corporate governance.

The position and its setting

Dr. Reddy’s Laboratories lists Head, Medical Affairs in Princeton, NJ, United States, under reference REF29751E. The details below separate the work described by the employer from essential conditions, preferred experience and practical preparation advice.

  • Employment type: Full-time
  • Employer listing date: 21 October 2026
  • Job Family: Medical Affairs & Pharmacovigilance
  • Brands: Dr Reddy's Laboratories Limited

Responsibilities and work described

  • Job Summary
  • Dr
  • Reddy's Laboratories is seeking a visionary Head of Medical Affairs, North America to build and lead the Medical Affairs organization supporting our portfolio of biosimilars, biologics, specialty pharmaceuticals, small-molecule and complex generics for Dr
  • Reddy’s North America Generics including Dr
  • Reddy’s Canada
  • 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 all North America products and pipeline assets
  • Leadership: medical launch readiness, evidence generation, publication planning, and scientific communications
  • Delivery: 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
  • Building: KOL engagement strategy, lead advisory boards, and represent Dr
  • Reddy's 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 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
  • Leadership: medical due diligence for licensing, acquisition, and portfolio expansion opportunities

Essential requirements and candidate background

  • Minimum work
  • 15+ years of progressive pharmaceutical/biopharmaceutical experience, including 5–10 years in Medical Affairs leadership
  • Skills & attributes:
  • Success leading Medical Affairs for product launches and building field medical teams
  • Ideal candidate to have prior Medical Affairs experience at both large and smaller pharma organizations
  • Therapeutic expertise in Oncology, Immunology/Rheumatology, Rare Disease, or Neurology
  • Knowledge: FDA regulatory pathways, promotional compliance, HEOR, and real-world evidence
  • Executive presence with communication, strategic thinking, and stakeholder management skills
  • Commitment to compliance, ethics, and patient-centered decision making

Education and qualification routes

  • Degree / qualification: Educational qualification: MD, DO, PharmD, or PhD required; board certification or post-doctoral clinical training preferred

Preferred experience and additional strengths

  • Experience across biosimilars, biologics, small-molecule/complex generics strongly preferred

Location, schedule and contract conditions

For this overseas or regional listing, confirm work authorisation and any location restrictions with the employer. The location does not establish visa sponsorship or permission to work remotely from India.

  • Work arrangement: On-site
  • Advertised location: Princeton, NJ, United States

Conditions requiring the complete notice

Some passages contain complex or combined conditions that have not been reduced to short eligibility statements here. Read the complete linked notice for those passages, including any alternatives, exceptions or restrictions. The concise facts above should not be treated as the full wording of every condition.

Pay and application dates

A verified salary figure is not established in this article. An online estimate for another Head, Medical Affairs vacancy is not an offer for reference REF29751E; use the employer’s own pay disclosure and recruitment communication.

A closing date is not confirmed in this article. Check the current employer page before submitting: an undated posting can change or be withdrawn.

How to apply to Dr. Reddy’s Laboratories

Applications follow the official employer page linked below.

Open the official Dr. Reddy’s Laboratories posting below and match the title and reference REF29751E.

Compare your qualifications and experience with the essential conditions for the Princeton, NJ, United States position, then read the preferred criteria separately.

Prepare an accurate CV and the supporting items requested in that employer’s application. Provide only information and documents you are authorised to share.

Use the employer’s application option, complete the required fields and review the submission. Retain the acknowledgement when one is provided. Job Alerts World does not receive the application.

Practical preparation: pharmacovigilance

A pharmacovigilance example should identify the process and your own responsibility for safety information, documentation or review. Discuss the work at a level that protects confidential case information.

Relevant skills

  • pharmacovigilance
  • regulatory affairs
  • pharmacy
  • compliance
  • business development
  • marketing
  • communication
  • training
  • stakeholder management
  • oncology

Important links

Official notification / job descriptionOpen official page
Online application portalOpen official page

Read the complete official notice before applying. Availability and requirements can change.

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