About the Role

　　The role profile is responsible for leading and supporting all activities related to Facilities, Procurement, Logistics and Licensing. Interact closely with REFS team and Site Leadership team for site Operations.

　　Your responsibilities include, but are not limited to:

　　• Identify opportunities to design and deploy solutions for increasing site productivity, CI pro-grams and lead site operational excellence (OPEX) projects.

　　• Identify opportunities to design and deploy CI programs for site. Work in collaboration with site and global strategy teams to deploy productivity initiatives for site.

　　• Function as Business liaison between Site and REF team. Ensure all legislative and regulatory licences are maintained and available for inspection on demand.

　　• Provide oversight for material management-import license coordination, sample shipment and receipt.

　　• Manage and coordinate capital equipment acquisition, installation, qualification, and staff training.

　　• Coordinate asset management (Asset verification, Asset write off /disposal) with finance/FRA. Responsible for supporting ARD and PHAD in Capex and Opex procurement /sourcing operations.

　　• Function as business Liaison between Site Engineering and business for all Engineering, HVAC, and MEP related works.

　　• Support ARD and PHAD with project management for Lab Upgrades, new projects, or facility adaptations. Responsible for Administration related CAPEX & OPEX planning, budgeting.

　　• Responsible for Coordination of compliance activities including site assistance to ARD, PHAD, QA for managing internal and /or external audits and any required remediation actions. Aware of Quality Management and GXP requirements.

　　Diversity & Inclusion / EEO

　　We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

　　Role Requirements

　　• BE (Mechanical) or equivalent, 10-15 Years of experience as a lead role in Site Operations, regulations, Logistics, manage Contracts and site Opex and Capex.

　　• Good knowledge of English and site language (oral and written).

　　• Recognized expertise in a GxP area and broad scientific as well as technical and strategic background.

　　• Demonstrated successful experience with working in interdisciplinary and cross-cultural teams.

　　• Demonstrated leadership and advanced coaching and mentoring skills.

　　• Thorough knowledge of relevant SOP, GMP and GXP regulations and policies if applicable.

　　• Excellent communication/presentation skills, Stakeholder management, Change management.

　　Why Novartis?

　　Our purpose is to reimagine medicine to improve and extend people's lives and our vision is to become the most valued and trusted medicines company in the world. How can we

　　achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture

　　Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network

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　　Division

　　Development

　　Business Unit

　　TECHNICAL R & D GDD

　　Location

　　India

　　Site

　　Hyderabad, AP

　　Company / Legal Entity

　　Nov Hltcr Shared Services Ind

　　Functional Area

　　Research & Development

　　Job Type

　　Full Time

　　Employment Type

　　Regular

　　Shift Work

　　No