Warman OBrien
Project Manager & Scheduler - CQV (Pharma/Biotech)
Warman OBrien - Baltimore, Maryland, United States, 21276
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Overview
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Overview
Project Manager & Scheduler - CQV (Pharma/Biotech)
Warman O'Brien is delighted to partner with a Leading Pharmaceutical Company seeking a Project Manager & Scheduler to oversee Commissioning, Qualification, and Validation (CQV) activities for a 12-month extendable project.
Responsibilities:
Develop and maintain CQV project schedules using Primavera P6, MS Project, or equivalent tools.
Align CQV activities with construction, installation, and operational readiness milestones.
Identify critical path activities, risks, and schedule bottlenecks, proposing mitigation strategies.
Track and report CQV progress, KPIs, and risk assessments to senior management.
Ensure GMP, GDP, FDA, and EMA compliance in all CQV scheduling activities.
Experience & Skills:
8+ years of project scheduling and management experience in CQV, commissioning, or validation.
Strong proficiency in Primavera P6, MS Project, and regulatory compliance (GMP, FDA, EMA).
Proven ability to coordinate multidisciplinary teams and manage complex pharma projects.
1099 Contract
Competitive Hourly Rate
Full time onsite - 40 hours per week
Start Date - April/May 2025
If you would like to be considered, please apply now to arrange for a confidential discussion with one of our recruiters!