RLT Project Manager

Novartis Sasayama, Japan

Company

Novartis

Location

Sasayama, Japan

Type

Full Time

Job Description

Summary

Responsible for developing strategies and implementing engineering activities in line with the business objectives of the Sasayama Operations and Novartis Manufacturing & Supply and RLT projects

About the Role

Major accountabilities:

  • Ensure all facilities, utilities and equipment are designed and operated in a safe and effective manner and are compliant with applicable standards
  • Lead innovation and reliability for Sasayama RLT operations
  • Support / implement Global Engineering initiatives and projects in Sasayama (ALCM, Standards, Best Practice Networks, Automation, Project Roadmap etc.).
  • Work closely with RLT Project Director and Campus Engineering Head to control and deliver major projects ensuring project objectives of scope, cost and schedule are maintained.
  • Develop facilities and equipment recapitalization plan for Sasayama RLT
  • Ensure that all facilities and equipment are designed and implemented fit for purpose operating standards, develop early asset management strategy during the project phase
  • Support / Lead cost for unit and operational efficiency initiatives for RLT Sasayama
  • Be part of the site RLT Ops leadership team that leads competitiveness journey to achieve long term performance
  • Ensure that process and equipment technology used in operations is consistent with product needs and people capability
  • Ensure sustainable internal operations through effective asset risk control and timely recapitalization of site assets to match product needs and 'Fit for Purpose'
  • Consistently apply a standard asset maintenance strategy across Divisions, to maintain design working conditions, reduce breakdowns and increase equipment life cycle
  • Develop / implement necessary organizational structure inline with global blueprints and campus dynamics
  • Manage baseload capital projects after site operations
  • Develop site qualification / commissioning plans and support site validation master plan

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Requirements:

  • 7+ years of general engineering experience thereof +5 years' experience in a pharmaceutical manufacturing environment specifically in the manufacturing of aseptic, radiopharmaceutical or customized medicine
  • Outstanding Technical knowledge with demonstrated ability to deliver safe and fully compliant technical solutions
  • Demonstrated Leadership abilities leading a team aligned around business/technology/project processes
  • Well-developed communication skills, able to present com-fortably to Senior Management and to Technical experts
  • Demonstrated with knowledge/understanding of key non-technical business processes, Human Relations, Finance
  • Advanced HSE and GxP/QA knowledge.
  • Business acumen, understanding value chain of manufacturing and applying risk based / fit for purpose solutions.

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

Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network

Benefits and Rewards: Read our handbook to learn about all the ways we'll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Division
Operations

Business Unit
Innovative Medicines

Location
Japan

Site
Sasayama

Company / Legal Entity
JP99 (FCRS = JP005) Ciba-Geigy Ltd.

Functional Area
Technical Operations

Job Type
Full time

Employment Type
Regular

Shift Work
No

Apply Now

Date Posted

01/12/2025

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