What are the responsibilities and job description for the Project Manager position at United Pharma Technologies Inc?
Job Title : Project Manager
Location: Pennsylvania, USA
Overview
We are seeking a Project Manager & Scheduler to lead the planning, coordination, and execution of Commissioning, Qualification, and Validation (CQV) activities for pharmaceutical and life sciences projects. This role ensures seamless integration of CQV timelines into overall project schedules while maintaining compliance with FDA, EMA, and GMP regulations.
Key Responsibilities
- Project Scheduling: Develop and manage CQV schedules using Primavera P6, MS Project, or similar tools.
- Coordination & Risk Management: Align CQV timelines with construction, installation, and operational readiness, identifying critical path activities and mitigating risks.
- Progress Tracking & Reporting: Monitor CQV progress, generate KPIs, dashboards, and risk assessments for stakeholders.
- Resource & Stakeholder Management: Optimize personnel and equipment allocation while adapting to schedule changes.
- Regulatory Compliance: Ensure adherence to GMP, GDP, FDA, and EMA requirements in CQV activities.
Qualifications & Experience
- Bachelor’s degree in Engineering, Project Management, or a related field.
- 8 years of experience in CQV project scheduling in pharmaceutical, biotech, or life sciences industries.
- Proficiency in Primavera P6, MS Project, and project scheduling tools.
- Strong knowledge of CQV processes, GMP compliance, and risk management.
- Excellent problem-solving, communication, and stakeholder management skills.
Preferred Qualifications
- PMP, PRINCE2, or equivalent certification.
- Experience managing large-scale biotech/pharmaceutical projects.
