Program Management

Job Description

Role Purpose

The Manager – Program Management is responsible for end-to-end coordination, tracking, and enablement of global regulatory filings and approvals across biosimilars and generic product portfolios. The role works in close partnership with Regulatory Affairs and cross-functional teams to ensure predictable execution of submissions, approvals, and lifecycle activities. In addition, the role provides technical program support to technology transfer (Tech Transfer) activities on a case-by-case basis, coordinating inputs across functions to enable smooth execution.

Key Responsibilities

1. Regulatory Filing & Approval Management

– Own global tracking of regulatory filings, approvals, commitments, and health authority queries across molecules and markets.

– Maintain molecule-wise and market-wise dashboards covering planned vs actual submissions and approvals.

– Ensure accuracy, clarity, and timely updates of regulatory status to stakeholders.

2. Cross-Functional Team (CFT) Orchestration

– Act as the primary coordination point between Regulatory Affairs, CMC, Clinical, Quality, Supply Chain, and Commercial teams.

– Identify critical path activities and interdependencies impacting submission and approval timelines.

– Drive action closure across teams and escalate risks with data-backed mitigation options.

3. Filing Readiness & Execution Governance

– Lead filing readiness checkpoints and support pre-submission planning activities.

– Coordinate internal reviews for submissions, responses to health authority questions, and lifecycle changes.

– Support execution discipline across submissions, variations, renewals, and post-approval commitments.

4. Technical Support for Tech Transfer Activities

– Provide program-level technical coordination support for technology transfer activities on a case-to-case basis.

– Coordinate inputs between CMC, MSAT, Manufacturing, Quality, Regulatory, and external partners during tech transfer phases.

– Track tech transfer milestones, dependencies, and regulatory touchpoints to ensure alignment with filing and approval timelines.

– Support documentation readiness and cross-functional alignment during initial transfers, site changes, or scale-up activities.

5. Reporting, Metrics & Leadership Communication

– Prepare leadership-ready dashboards, summaries, and updates for governance and review forums.

– Track execution KPIs such as on-time filings, approval timelines, and query closure metrics.

– Highlight trends, risks, and opportunities for continuous improvement.

6. Regional & Partner Coordination

– Support coordination with regional affiliates and external partners to enable local submissions and approvals.

– Ensure alignment between global regulatory plans and regional execution requirements.

Qualifications & Experience

Education

Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, Engineering, or a related discipline.

Experience

• 13+ years of experience in Program Management, Regulatory Operations, or Regulatory Enablement roles within the pharmaceutical or biotechnology industry.
• Hands-on exposure to global regulatory submissions, approvals, and lifecycle management activities.
• Experience supporting biosimilars and/or biologics portfolios is preferred.
• Exposure to tech transfer or site change activities is an advantage.

Key Skills & Competencies

– Strong understanding of regulatory submission and approval lifecycle.

– Working knowledge of CMC, manufacturing, and quality concepts relevant to regulatory filings and tech transfer.

– Excellent cross-functional coordination and stakeholder management skills.

– Strong execution, tracking, and analytical skills.

– Ability to communicate clearly with senior stakeholders.

– Proficiency in Excel-based trackers, dashboards, and PowerPoint reporting.

– Exposure to MOW marketShow more

• Seniority levelAssociate
• Employment typeFull-time
• IndustriesPharmaceutical Manufacturing and Manufacturing