Job Description

  • Lead end-to-end project management for IT/technology initiatives in the pharma/life sciences domain, ensuring timely delivery and within budget.
  • Collaborate with cross-functional teams including R&D, Quality, Manufacturing, Regulatory, and Commercial teams.
  • Define project scope, objectives, deliverables, milestones, and timelines.
  • Manage vendor coordination, software implementation, system integration, and infrastructure deployments.
  • Ensure alignment of projects with industry regulations such as GxP, CFR Part 11, HIPAA, GDPR, etc.
  • Prepare detailed project plans, status reports, risk mitigation strategies, and issue logs.
  • Act as a single point of contact for stakeholders, ensuring effective communication and expectation management.
  • Facilitate change management, training, and adoption strategies.
  • Ensure adherence to internal project governance, compliance, and validation procedures.

Requirements

  • 10–12 years of total experience in IT/Technology Project Management, with at least 5 years in the Pharma/Life Sciences domain.
  • Proven experience managing technology transformation, digital health, lab systems (e.g., LIMS, ELN), clinical systems (e.g., CTMS), manufacturing systems or similar.
  • Strong understanding of regulatory environments and compliance standards (FDA, GxP, CSV, etc.).
  • Hands-on experience with Agile, Scrum, or Hybrid delivery methodologies.
  • Ability to manage cross-functional teams and third-party vendors.
  • Excellent communication, stakeholder management, and leadership skills.
  • PMP/Prince2/CSM certification is a plus.

Good to Have:

  • Experience with data platforms, analytics in pharma, or AI/ML initiatives in life sciences.
  • Exposure to cloud migrations, enterprise platforms like SAP, Veeva, Oracle Health Sciences, etc.
  • Prior experience with global project rollouts across geographies.
  • Understanding of pharma manufacturing processes, quality control, or clinical development lifecycle.

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