Project Manager – Europe Business Development & Portfolio Management

Glenmark Pharmaceuticals

Mumbai

Vor Ort

INR 1.800.000 - 3.200.000

Vollzeit

vor 29 Stunden
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Zusammenfassung

Glenmark Pharmaceuticals seeks a senior Business Development professional to support Europe BD activities, including managing portfolio selection, regulatory alignment, and due diligence for in-licensing opportunities. The role emphasizes cross-functional coordination and governance without client-facing duties.

The ideal candidate has 6+ years in pharma BD, experience with European generics development, and proficiency in data analytics to drive strategic decisions across the portfolio

Qualifikationen

  • Experience with IQVIA/IMS data analysis and market insights in BD context.
  • Knowledge of European generic formulation development processes and project management.
  • Strong exposure to due diligence, portfolio management and in-licensing activities.

Aufgaben

  • Manage the annual Europe Portfolio selection exercise.
  • Manage RA withdrawal contract termination process.
  • Coordinate cross-functional evaluations and consolidate business cases for BD/In-Licensing.
  • Support due diligence and regulatory/commercial alignment for projects.
  • Prepare MIS and leadership updates on BD initiatives.

Kenntnisse

IQVIA/IMS data analysis
European generic formulation

Ausbildung

M.Pharm

Jobbeschreibung

To support the Business Development Europe team by managing and monitoring in-licensing contract terminations and MA withdrawals, consolidating BD budget and Long-Range Plan activities, coordinating and managing the annual portfolio-selection exercise for Europe, coordinating CAPEX governance for BD, supporting the Head of BD/In-Licensing with scouting for M&A and strategic in-licensing opportunities, coordinating due diligence and business-case consolidation, coordinating regulatory and commercial activities (including trade-dress checks), and tracking progress across in-house projects. This is not primarily a client-facing BD role.

OVERALL JOB RESPONSIBILITIES
  • Manage the annual Europe Portfolio selection exercise
  • Manage RA withdrawal contract termination process.
  • Manage trade name and trade dress evaluations.
  • Maintain portfolio trackers and dashboards.
Business Development Scouting
  • Analyse tail-end Big Pharma brands using IQVIA/IMS data.
  • Conduct initial evaluation scouting and initial partner engagement for M&A opportunities
  • Prepare and consolidate business cases and power point presentations for M&A projects
  • Support Scout for distribution opportunities before handover to IL team.
Business Development & Strategic Projects
  • Manage due diligence for M&A and strategic in-licensing opportunities.
  • Coordinate cross-functional evaluations and consolidate business cases.
  • Support commercial, technical and regulatory assessments.
Reporting & Governance
  • Compile, Consolidate and coordinate the LRP data on new projects with finance and Launch.
  • Prepare MIS, leadership presentations and project trackers.
  • Provide governance updates and risk reporting to senior management
European Development Project Management
  • Evaluate IH project plans and manage timelines, risks and resources.
  • Coordinate R&D, Regulatory, Supply Chain, QA, Clinical and Commercial teams.
  • Ensure on-time EB execution, Pilot batches, Pivotal studies and Dossier submission.
  • Ensure complete handover of the projects to Launch team with alignment with the Projects team
KEY INTERFACES / INTERACTIONS
Internal Stakeholders
  • BD IH/ IL teams
  • Supply Chain
  • Regulatory Affairs
  • Project Management
  • Europe Country Heads
  • R&D
  • Analytical
  • IPM
  • Demand Planning
  • Manufacturing
  • QA
  • QC
  • Clinical
  • Marketing
  • Finance
KNOWLEDGE, SKILLS AND ABILITIES
Education

M.Pharm

Experience
  • 6+ years in the pharmaceutical industry.
  • Experience in European generic formulation development and project management.
  • Exposure to Business Development, Due Diligence, Portfolio Management or In-Licensing preferred.
Knowledge & Skills
  • IQVIA/IMS data analysis.
  • European Generic Formulation Development process.
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