What are the responsibilities and job description for the Project Manager & Scheduler – CQV (Pharma/Biotech) position at Warman O’Brien?
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!
