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Location: Pittsburgh, Pennsylvania (PA)
Contract Type: C2C
Posted: 4 days ago
Closed Date: 03/17/2026
Skills: QC / QA Pharmacovigilance CSV / GxP IT systems
Visa Type: Any Visa

Role- Project Manager

Location- Pittsburgh, PA (Onsite) – LOCALS only

Duration- Long term contract

 

Required Skills & Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Engineering, or related field (Master’s preferred).
  • 5–12 years of experience in project management within pharma, biotech, CRO, or medical devices.
  • Strong domain knowledge in one or more:
  • Drug discovery & development
  • Clinical trials / Clinical Operations
  • Regulatory Affairs
  • Pharma manufacturing / QC / QA
  • Pharmacovigilance
  • CSV / GxP IT systems
  • Practical understanding of FDA, ICH, GxP, 21 CFR Part 11, and pharma SDLC/validation processes.
  • Proficiency with PM tools: MS Project, Jira, Smartsheet, Confluence, Veeva Vault (plus).
  • Strong communication, leadership, analytical, and stakeholder management skills.
  • PMP, PRINCE2, CSM, or industry-specific certifications preferred.