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Navixus | Tech Mahindra

Program Manager

Posted 3 Hours Ago
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Hybrid
Sunnyvale, CA
Expert/Leader
Hybrid
Sunnyvale, CA
Expert/Leader
Lead large-scale, cross-functional life sciences programs across R&D, manufacturing, quality, and regulatory. Define roadmaps, budgets, governance; manage stakeholders, vendors, risks, and KPIs. Ensure GxP and regulatory compliance (FDA/EMA, 21 CFR Part 11, EU Annex 11), audit readiness, and adherence to SDLC/CSV/CSA for digital programs.
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Job Summary
Program Manager
FUll Time

The pay range for this role is $180K Max per annum including any bonuses or variable pay. Tech Mahindra also offers benefits like medical, vision, dental, life, disability insurance and paid time off (including holidays, parental leave, and sick leave, as required by law). Ask our recruiters for more details on our Benefits package. The exact offer terms will depend on the skill level, educational qualifications, experience and location of the candidate.

Job Summary
We are seeking a highly experienced Program Manager with 15+ years of experience in the Life Sciences / Pharmaceutical domain to lead large scale, cross functional programs. The ideal candidate will be responsible for driving strategic initiatives, ensuring GxP compliance, managing stakeholders, and delivering complex projects across R&D, manufacturing, quality, and regulatory functions.
Key Responsibilities
✿ Program & Portfolio Management
  • Lead and manage multiple large scale programs/projects across Life Sciences value chain
  • Define program roadmap, scope, timelines, budget, and resource allocation
  • Ensure successful delivery of programs aligned with business goals
  • Establish governance frameworks and reporting structures
Stakeholder Management
  • Engage with senior leadership, business stakeholders, and cross functional teams
  • Act as a primary point of contact for program status, risks, and escalations
  • Manage vendor and third party relationships
Regulatory & Compliance Oversight
  • Ensure programs comply with:
    • GxP (GMP, GLP, GCP) requirements
    • FDA, EMA regulations
    • 21 CFR Part 11, EU Annex 11 (for digital programs)
  • Drive audit readiness and support regulatory inspections
Delivery & Execution
  • Drive end to end program execution across:
    • Clinical, R&D, Manufacturing, Supply Chain, Quality
  • Monitor KPIs, milestones, risks, and dependencies
  • Ensure adherence to SDLC / CSV / CSA methodologies (if IT/digital programs)


Tech Mahindra is an Equal Employment Opportunity employer. We promote and support a diverse workforce at all levels of the company. All qualified applicants will receive consideration for employment without regard to race, religion, color, sex, age, national origin, or disability. All applicants will be evaluated solely based on their ability, competence, and performance of the essential functions of their positions with or without reasonable accommodations. Reasonable accommodation also are available in the hiring process for applicants with disabilities. Candidates can request a reasonable accommodation by contacting the company ADA Coordinator at [email protected] .

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