What are the responsibilities and job description for the Pharmaceutical CQV Project Manager position at IT Engagements,Inc.?
Greetings from IT Engagements
Job Title: CQV Project Manager/Program Manager (NO H1B)
Location: Mount Vernon, IN
KEY RESPONSIBILITIES
Capital Project Management:
Lead and manage full lifecycle of capital projects, including planning, budgeting, execution, and closeout, ensuring alignment with site and corporate goals
Technical Leadership:
Oversee engineering activities for projects including, but not limited to: Facilities/Utilities supporting Oral Solid Dosage Manufacturing and Packaging, GMP processes, Automation upgrades, and QC Lab equipment.
Budget & Financial Oversight:
Develop and maintain accurate project budgets and forecasts; monitor project spend, track variances, and ensure financial accountability for capital expenditures.
Documentation & Phase Deliverables:
Ensure adherence to established project documentation, phase gates, and change management processes for technical and operational projects.
Cross-Functional Collaboration:
Partner with Manufacturing, Quality, Validation, and other cross-functional stakeholders to deliver integrated project outcomes and support site readiness for commercial and clinical operations.
Vendor & Contractor Management:
Manage external engineering firms, equipment vendors, and contractors to ensure adherence to project scope, quality, safety, and schedule requirements.
Education:
Bachelor’s degree in Engineering (Mechanical, Chemical, Industrial, or related discipline). Advanced degree preferred.
Experience:
- Minimum 7–10 years of experience in pharmaceutical manufacturing with a focus on Oral Solid Dosage Manufacturing and Packaging, GMP processes, Automation upgrades, and QC Lab equipment.
- Proven track record in capital project management, managing multiple projects at once.
Technical Expertise:
- Strong understanding of Facilities/Utilities supporting Oral Solid Dosage Manufacturing and Packaging, GMP processes, Automation upgrades, and QC Lab equipment.
- Knowledge of pharmaceutical packaging, modern controls and safety devices, tablet inspection systems, SCADA/PAS-X integrations, and equipment validation.
- Familiarity with process utilities and equipment qualification protocols (IQ/OQ/PQ).
Project & Financial Skills:
- Highly skilled utilizing Microsoft Project for schedule/project plan development.
- Skilled in budgeting, forecasting, and cost control within complex, regulated environments.
Soft Skills:
- Strong leadership and communication skills, with the ability to influence cross-functional teams.
- Highly organized, detail-oriented, and capable of managing multiple priorities in a dynamic environment.
Other:
- Willingness to work onsite at a GMP manufacturing facility
Thank you
vinaya@itengagements.com
Job Type: Contract
Pay: $65.00 - $70.00 per hour
Expected hours: 40 per week
Work Location: In person
Salary : $65 - $70