Digital Transformation Manager (Permanent)

gmp technologies (s) pte ltd; Singapore; On-site; SGD 120,000 - 180,000; Full time

Job summary

GMP Technologies (S) Pte Ltd is seeking a senior digitalization and ERP lead to develop and execute the site's roadmap, integrating ERP/SCADA/MES workflows. The role requires strong GMP/GxP and CSV expertise and a track record in pharmaceutical manufacturing digitalization.

You will partner with IT, Manufacturing, Quality, Engineering, and Supply Chain to deliver complex, multi-vendor projects, ensuring compliance, data integrity, and timely delivery in a highly regulated environment.

Qualifications

• Bachelor's or Master's degree in Computer Science, Information Technology, or related discipline.
• Minimum 5 years of ERP implementation/management experience (SAP/Oracle).
• Minimum 3 years of digitalization project experience in pharmaceutical manufacturing.
• Strong understanding of GMP/GxP, CSV, and data integrity requirements.

Responsibilities

• Develop and implement the site's digitalization roadmap aligned with business and operations.
• Drive integration and optimization of ERP, HR, SCM, MES, SCADA systems.
• Lead end-to-end ERP implementation, upgrade, integration, and maintenance (SAP/Oracle).
• Ensure system architecture, performance, and regulatory compliance.
• Lead manufacturing systems (MES, WMS, SCADA) implementation and maintenance.
• Drive digitalization to improve efficiency, data visibility, and traceability.
• Collaborate with IT, Manufacturing, Quality, Engineering, and Supply Chain teams.
• Coordinate resources, vendors, and system integrators for projects.
• Ensure systems comply with GMP/GxP and FDA/EMA regulations.
• Oversee CSV and maintain data integrity throughout lifecycles.
• Manage multiple digitalization projects within scope, budget, and timelines.
• Monitor progress, mitigate risks, and coordinate stakeholders to milestones.

Skills

ERP implementation

Project management

GMP/GxP knowledge

CSV/data integrity

SCADA/MES/WMS

Regulatory compliance

Vendor management

Education

Bachelor's or Master's degree in Computer Science or IT

Tools

SAP/Oracle ERP

SCADA

MES

WMS

CSV validation tools

Job description

Responsibilities

• Develop and implement the site's digitalization roadmap in alignment with business and operational objectives.
• Drive integration and optimization of enterprise and manufacturing systems, including ERP, HR, SCM, MES, and SCADA.
• Lead end-to-end ERP implementation, upgrade, integration, and maintenance (e.g., SAP/Oracle).
• Ensure system architecture, performance, and functionality meet business and regulatory requirements.
• Lead the implementation, upgrade, integration, and maintenance of manufacturing systems, including MES, WMS, and SCADA.
• Drive manufacturing process digitalization to improve operational efficiency, data visibility, and production traceability.
• Collaborate with IT, Manufacturing, Quality, Engineering, and Supply Chain teams to drive digital initiatives.
• Coordinate internal resources, external vendors, and system integrators to ensure effective project execution.
• Ensure digital systems comply with pharmaceutical GMP/GxP requirements and applicable FDA/EMA regulations.
• Oversee computerized system validation (CSV) and ensure data integrity throughout the system lifecycle.
• Manage multiple digitalization projects, ensuring delivery within agreed scope, budget, and timelines.
• Monitor project progress, manage risks, and coordinate stakeholders to achieve project milestones.

Qualifications

• Bachelor's or Master's degree in Computer Science, Information Technology, or a related discipline.
• Minimum 5 years of experience in ERP implementation and management (SAP/Oracle), including system architecture and integration.
• Minimum 3 years of digitalization project experience in pharmaceutical manufacturing.
• Strong understanding of GMP/GxP, computerized system validation (CSV), and data integrity requirements
• Experience with manufacturing systems such as MES, WMS, or SCADA.
• Strong project management, organizational, and problem-solving skills.
• Proven ability to manage cross-functional teams, vendors, and multiple projects.
• Excellent communication and stakeholder management skills.
• PMP or PRINCE2 certification is an advantage.
• Experience in multinational pharmaceutical companies or CDMO manufacturing environments.
• Knowledge of pharmaceutical drug discovery and process development.
• Familiarity with AI/ML and data analytics applications in manufacturing.

We regret that only shortlisted candidates will be notified.

GMP Technologies (S) Pte Ltd | EA License: 11C3793 | EA Personnel: Bautista Gia Grace De Guzman | Registration No: R23111973

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