Job Description

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!

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