consultpharmatek
New Brunswick, United States | Posted on 10/02/2024
Industry Pharma/Biotech/Clinical Research
Job Type Contract
Work Experience 5+ years
State/Province New Jersey
Country United States
Job Description
We are seeking a Senior ProjectManager with extensive experience in managing CapEx projects within the pharmaceutical industry. The role involves overseeing project schedules, budgets, and reporting for a complex CQV initiative. The Project Manager will work closely with cross-functional teams, ensuring alignment with project milestones and regulatory compliance. Key Responsibilities
Develop, manage, and maintain the project schedule, budget, and financial tracking. Coordinate cross-functional teams including CQV, engineering, and construction. Lead project reporting activities, including regular updates to stakeholders on project status, risks, and budget adherence. Monthly schedule and cost reporting incl. cash flow curves and resource utilization (mobilization) Facilitate communication between construction, engineering, and validation teams. Manage project changes, ensuring documentation and approvals align with company standards. Implement risk management processes to mitigate project delays or cost overruns. Requirements
Qualifications
Bachelor’s degree in Engineering, Project Management, or related field. 10+ years of experience managing CapEx projects in the pharmaceutical industry. Strong background in commissioning, qualification, and validation (CQV). Proficient in project management tools (e.g., MS Project) and methodologies. Excellent communication and stakeholder management skills. PMP certification is a plus. Excellent documentation and communication skills
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We are seeking a Senior ProjectManager with extensive experience in managing CapEx projects within the pharmaceutical industry. The role involves overseeing project schedules, budgets, and reporting for a complex CQV initiative. The Project Manager will work closely with cross-functional teams, ensuring alignment with project milestones and regulatory compliance. Key Responsibilities
Develop, manage, and maintain the project schedule, budget, and financial tracking. Coordinate cross-functional teams including CQV, engineering, and construction. Lead project reporting activities, including regular updates to stakeholders on project status, risks, and budget adherence. Monthly schedule and cost reporting incl. cash flow curves and resource utilization (mobilization) Facilitate communication between construction, engineering, and validation teams. Manage project changes, ensuring documentation and approvals align with company standards. Implement risk management processes to mitigate project delays or cost overruns. Requirements
Qualifications
Bachelor’s degree in Engineering, Project Management, or related field. 10+ years of experience managing CapEx projects in the pharmaceutical industry. Strong background in commissioning, qualification, and validation (CQV). Proficient in project management tools (e.g., MS Project) and methodologies. Excellent communication and stakeholder management skills. PMP certification is a plus. Excellent documentation and communication skills
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