摘要
About the Role
Key Responsibilities:
- Develop a comprehensive project scope statement, deliverable list, man-hour estimates, and cost estimates for design projects.
- Lead the preparation and delivery of the kick-off meeting presentation, ensuring alignment with project objectives and scope.
- Prepare and manage project management documents such as the project charter, PSS, PMP, risk register, and organization chart.
- Help outline project scope, objectives, and deliverables to ensure alignment with project goals.
- Support the creation of detailed project plans and timelines for design and construction phases, ensuring timely completion and adherence to deadlines.
- Coordinate with vendors and contractors in collaboration with the Purchasing team, assisting in issuing inquiries, conducting technical discussions, and collecting offers.
- Accurately calculate the total project cost, ensuring all aspects of design, construction, and regulatory compliance are accounted for.
- Ensure designs comply with pharmaceutical regulations (e.g., GMP, FDA, EMA) under supervision.
- Facilitate timely review and approval processes with internal and external stakeholders and cross-functional teams.
- Proactively identify and address risks related to design, cost, and regulatory compliance throughout the project lifecycle.
- Ensure that project documents, including design specifications, contracts, and compliance documentation, are accurately prepared and maintained.
Essential Requirements:
- 8-12 years of pharmaceutical Green Field/ Brown Field project Experience.
- High level Understanding of Engineering like HVAC, Electrical, Civil & Automation
- Basic Layout understanding of Aseptic and Biologics facility with regulatory compliance
- Assist in ensuring CAPEX projects of are delivered on time and within budget, while meeting quality standards.
- Support the completion of project reviews on schedule, ensuring that no critical observations arise.
- Contribute to the development of business cases for CAPEX projects, assisting in the approval process.
- Assist in providing timely and accurate progress reports to project managers and stakeholders.
Desirable Requirement:
- Candidate should be Engineering Degree with 8-10 years of experience.
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
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Accessibility and accommodation
Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
