Engineering Validation Lead — GMP Leadership

Lonza Group Ltd.; Singapore; On-site; SGD 120,000 - 180,000; Full time

Benefits offered by this job

Agile culture

Inclusive workplace

Compensation programs

Global benefits

Job summary

Lonza Group Ltd. in Singapore (Tuas) is seeking an Associate Manager, Engineering – Validation to lead the validation of facility, equipment, and utilities, ensuring the site Validation lifecycle complies with regulatory requirements.

You will supervise day-to-day validation activities, collaborate across departments, and participate in inspections and audits to uphold high quality and safety standards in medicines manufacturing.

Qualifications

• Degree in Engineering or Life Science or related discipline, or work experience in pharmaceutical validation.
• Leadership/managerial experience for direct reports.
• Knowledge of cGMP industry practices and requirements.
• Strong problem-solving, troubleshooting, and analytical skills.
• Ability to work cross-functionally and manage multiple priorities.

Responsibilities

• Supervise and manage day-to-day Validation activities per approved SOPs, plans and policies.
• Review and approve Validation SOPs and Plans to support the Validation Master Plan.
• Manage internal and external validation resources to meet department goals.
• Coordinate with system owners, quality unit and other departments to align scope, execution and reporting of Validation Program.
• Plan and conduct on-job training for staff and identify training gaps.

Skills

People management

cGMP knowledge

Problem solving

Cross-functional work

Prioritization

Education

Engineering or Life Science degree

Job description

Lonza Group Ltd. in Singapore (Tuas) is seeking an Associate Manager, Engineering – Validation to lead the validation of facility, equipment, and utilities, ensuring the site Validation lifecycle complies with regulatory requirements.

You will supervise day-to-day validation activities, collaborate across departments, and participate in inspections and audits to uphold high quality and safety standards in medicines manufacturing.