Job ID: JOB_ID_687
Role Overview
We are seeking a highly skilled Technical Project Manager to lead a critical Pharmaceutical Validation project in Rensselaer, NY. This onsite role requires a deep understanding of GxP environments and the technical nuances of manufacturing execution systems. The Project Manager will be responsible for overseeing capital-scale projects, ensuring that all systems meet stringent CSV/CSA validation standards while maintaining strict adherence to project schedules and budgets.
Key Responsibilities
- Lead the planning and execution of technical projects within a pharmaceutical manufacturing environment, focusing on Rockwell and Factory Talk Batch systems.
- Ensure all project activities comply with Computer System Validation (CSV) and Computer Software Assurance (CSA) protocols.
- Develop and maintain detailed project schedules using Project 2021, tracking milestones and resource allocation for capital-scale initiatives.
- Collaborate cross-functionally with Engineering, Quality Assurance, and IT departments to ensure seamless system integration and compliance.
- Manage the full project lifecycle from initial requirements gathering through deployment and final validation reporting.
- Utilize Jira for task tracking, issue management, and agile reporting within the project framework.
- Communicate project status, risks, and mitigation strategies to senior leadership and external stakeholders.
Technical Requirements
- At least 5 years of experience in Technical Project Management within the pharmaceutical or life sciences industry.
- In-depth technical understanding of Rockwell Automation platforms and Factory Talk Batch from a project leadership perspective.
- Proven expertise in CSV/CSA validation methodologies and GxP regulatory requirements.
- Extensive experience in project planning and scheduling for large-scale capital projects.
- Familiarity with Plant PAX and other industrial automation solutions is a significant plus.
Professional Qualifications
- Strong leadership skills with the ability to drive results in a highly regulated and fast-paced environment.
- Excellent verbal and written communication skills, with a focus on technical documentation and stakeholder management.
- Ability to work onsite in Rensselaer, NY, for the duration of the 12-month contract.
- Bachelor’s degree in a technical or scientific discipline is preferred.
Special Requirements
Visa Constraint: No H1B; Onsite requirement; Domain: Pharmaceuticals/GxP.
Compensation & Location
Salary: $140,000 – $185,000 per year (Estimated)
Location: Rensselaer, NY
Recruiter / Company – Contact Information
Recruiter / Employer: Stellent IT LLC
Email: aditya@stellentit.com
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