Expert, Supply Chain

3 days ago

Singapur, Singapore Lonza Full time

Overview

Lonza is seeking an Expert, Supply Chain - ERP & Supply Chain Transformation (Fixed Term Contract) for a 15 months fixed term contract at the Tuas site in Singapore.

There is a focus on gaining exposure to cutting-edge biotechnology and innovation, manufacturing therapeutic proteins under cGMP conditions, and contributing to data integrity and ERP-related initiatives within the Supply Chain team.

What You’ll Do
  • Responsible for the creation and maintenance of various SAP master data, including material master, vendor master, resource master, BOM, recipe, and PV.
  • Ensure the integrity of SAP master data, implement data governance KPIs and dashboards, and develop action plans to continuously improve data quality.
  • Ensure that SOPs and workflows related to new part setups, BOMs, and recipe creations are current, accurate, and practical for end users.
  • Monitor workflow progress to ensure all materials pass through designated approval streams, complying with GMP requirements.
  • Manage the full lifecycle of part numbers (PN), including deactivation, reactivation, and discontinuation of parts in the ERP system.
  • Provide hands-on support to SAP users, ensuring material master data accuracy and consistency.
  • Proactively identify and implement workflow process improvements to reduce lead time and drive operational excellence.
  • Serve as the SME for the ERP system, focusing on best practices and processes for new material creation.
  • Collaborate with all relevant stakeholders requiring new materials and serve as the key user for any ERP-related projects.
  • Assess production feasibility, calculate costings, and perform variance checks to ensure the accuracy of master data and BOMs.
  • Act as the primary representative for the function during regulatory inspections and quality audits, ensuring compliance and effective communication.
  • Collaborate with cross-functional teams to identify and resolve data integrity issues.
  • Continuously evaluate and improve data integrity processes to enhance overall quality assurance efforts.
  • Monitor data processing procedures to ensure compliance with data integrity standards.
  • Implement robust data quality controls to maintain the accuracy and reliability of information.
  • Develop and maintain documentation outlining data integrity protocols and procedures.
  • Provide training and guidance to colleagues on best practices for maintaining data integrity.
What We’re Looking For
  • 5-10 years experience, with 4-5 years hands on SAP experience
  • Relevant pharma industry experience is preferred
  • Strong problem solving ability, troubleshooting and analytical skills
  • Planning/Work Management
  • Communication - present facts clearly, logically & accurately so that it can be understood by others

Reference: R69897

Seniority level
  • Not Applicable
Employment type
  • Contract
Job function
  • Management and Manufacturing
Industries
  • Pharmaceutical Manufacturing

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