Benchtop CI Lead CW Role

Advanced Manufacturing Tech Solutions PTE. LTD. (AMTSOL); Singapore; On-site; SGD 89,000 - 123,000; Full time

Job summary

AMTSOL is seeking a hands-on Benchtop CI Lead CW to support GMP Benchtop and Analytical Systems on a 6-month contract in Singapore. You will collaborate with the Benchtop Team Lead to coordinate improvement projects, track actions, and ensure timely delivery while maintaining compliance.

The role emphasizes hands-on Laboratory IT support and cross-functional coordination with Quality, Manufacturing, Engineering, and Vendors to drive efficiency, develop standard templates, and report on progress

Qualifications

• Bachelor's degree in IT/engineering or life sciences.
• Minimum 5 years of experience supporting Laboratory IT, Benchtop Systems, Analytical Instruments, or GMP Computerized Systems.
• Experience coordinating projects or cross-functional workstreams in a regulated environment.

Responsibilities

• Lead and coordinate Benchtop CI projects with plans, milestones, risks, and action tracking.
• Support Team Lead to maintain priorities and follow-ups for activities, deviations, and actions.
• Analyze processes to reduce delay, remove duplication, and implement compliant improvements.
• Coordinate with Laboratory Ops, Quality, Manufacturing, Eng, Infrastructure, vendors, and owners.
• Develop tools: action logs, trackers, dashboards, templates for projects.
• Provide hands-on technical support for GMP Benchtop and Analytical Systems.

Skills

Project coordination

Stakeholder management

Continuous improvement

GMP knowledge

Analytical thinking

Education

Bachelor's degree in IT/Engineering/Life Sciences

Tools

CSV familiarity

GMP systems

Lab IT tools

Job description

Role: Benchtop CI Lead CW

Role Summary

We are looking for a hands-on Laboratory IT professional with strong project coordination, stakeholder management, and continuous improvement skills to support GMP Benchtop and Analytical Systems for a 6-Month Contract (Extendable). The successful candidate will support the Benchtop Team Lead to coordinate improvement projects, drive action closure, and improve work processes and operational efficiency.

Key Responsibilities

• Lead and coordinate defined Benchtop continuous improvement projects, including project plans, milestones, risks, actions, benefits tracking, and timely status reporting.
• Support the Benchtop Team Lead to maintain clear work priorities, action tracking, and follow-up for planned activities, projects, deviations, and improvement actions.
• Analyse current support processes to identify duplicated work, unclear handoffs, manual steps, and recurring causes of delay or rework; implement practical and compliant improvements.
• Coordinate with Laboratory Operations, Quality, Manufacturing, Engineering, Infrastructure, vendors, System Owners, and Business Owners to align on project priorities, requirements, decisions, and timelines.
• Develop and maintain practical project tools, such as action logs, trackers, work plans, process maps, dashboards, and standard templates.
• Provide hands-on technical support and troubleshooting for GMP Benchtop and Analytical Systems as required.

Minimum Qualifications

• Bachelor's degree in information technology, Computer Engineering, Automation, Instrumentation, Life Sciences, or related discipline.
• Minimum 5 years of experience supporting Laboratory IT, Benchtop Systems, Analytical Instruments, or GMP Computerized Systems.
• Demonstrated experience coordinating projects, improvement initiatives, or cross-functional workstreams in a regulated environment.

Preferred Skills

• Strong Laboratory IT background with project coordination and stakeholder management experience.
• Experience supporting pharmaceutical or biotechnology manufacturing environments.
• Knowledge of Lean, Kaizen, process mapping, or similar continuous improvement methods.
• Familiarity with CSV, GMP computerized systems, data integrity, and deviation/CAPA processes.

Key Skills

• Strong project coordination, organisation, and follow-through on actions and commitments.
• Ability to structure ambiguous work, identify risks early, and communicate clear options and recommendations.
• Practical problem-solving skills with the ability to simplify processes while maintaining GMP compliance.
• Strong communication, stakeholder management, and technical documentation skills.