About the Opportunity
Pharmadose Generics LLP is seeking a highly experienced and commercially-minded Senior Legal Manager to lead its global contracting, dispute management, and corporate regulatory strategy. Reporting directly to the CEO, this role offers an extraordinary opportunity for a seasoned pharmaceutical legal professional to take full ownership of high-stakes global contracts, manage international counterparties, and safeguard the company's commercial interests across regulated and emerging markets.
About Pharmadose Generics LLP
Pharmadose is a global B2B pharmaceutical power partner with over 27 years of industry expertise. Enabling sustainable growth across the global pharmaceutical landscape, Pharmadose collaborates with international partners across product development, registration, licensing, supply, and commercialization. Built on regulatory discipline, quality governance, and long-term strategic relationships, Pharmadose helps pharmaceutical companies navigate complex global market requirements with utmost confidence and compliance.
Key Responsibilities
- Global Contracting: Independently draft, review, and negotiate complex CDMO agreements (manufacturing, supply, licensing, and technology transfer) alongside CRO and master service development agreements.
- Contract Governance: Prepare CDAs/NDAs, maintain a rigorous contract repository, and track legal obligations across all global commercial arrangements.
- Dispute Management & External Counsel Oversight: Formulate pre-litigation strategies, manage commercial disputes, and coordinate external legal counsel across India, the United States, and other international jurisdictions while optimizing legal spend.
- Regulatory & IP Coordination: Support regulatory-adjacent legal matters, including Paragraph IV / patent-related litigation support in coordination with specialized IP counsel, and ensure strict compliance with global data-protection obligations.
- Strategic Advisory: Serve as a trusted legal advisor to promoters and senior management, providing sound business judgment and cross-border strategic counsel.
Eligibility & Requirements
- Education: Bachelor of Laws (LLB) required; Master of Laws (LLM) strongly preferred.
- Experience: 8 to 10 years of focused legal experience in a pharmaceutical company or a top-tier law firm serving pharma clients.
- Domain Expertise: Hands-on expertise drafting and negotiating CDMO/CRO, technology transfer, and licensing agreements.
- US Market Knowledge: Working knowledge of US pharmaceutical commercial arrangements (wholesaler, GPO, and distribution agreements) is highly desirable.
- IP Fundamentals: Deep understanding of intellectual property fundamentals including patents, trade secrets, and tech-transfer mechanics in pharma contracts.
How to Apply
Interested candidates who meet the qualifications are invited to apply directly via the official LinkedIn listing before the deadline on October 18, 2026. Early applications are strongly encouraged.