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| Advertiser Name | Warman OBrien | | Advertiser Type: | Agency |
| Classification: | 6227 | | Subclassification: | |
| Country: | United States | | Location: | United States |
| Language: | English - United Kingdom (en-GB) | | Contact Name: | |
| Employment Type: | Permanent | | Workhours: | Full Time |
Position: Project Manager & Scheduler - CQV (Pharma/Biotech) |
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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