Site Validation Engineering Lead

Lonza; Singapore; On-site; Confidential; Full time

Benefits offered by this job

Agile culture

Inclusive workplace

Competitive compensation

Role/location benefits

Job summary

Lonza Singapore Tuas is seeking an Associate Manager, Engineering - Validation to lead the validation lifecycle for facilities, equipment and utilities, ensuring regulatory compliance. This on-site role provides leadership over routine validation activities and supports real-time collaboration to maintain high quality and safety in medicines manufacturing.

Based in Singapore, you will supervise day-to-day validation tasks, review SOPs and plans, manage internal and external resources, train

Qualifications

• Degree in Engineering or Life Science or related discipline or work experience in pharmaceutical validation role.
• People management experience and leadership responsibilities for direct reports.
• cGMP industry knowledge.
• Strong problem-solving, troubleshooting, and analytical skills.
• Ability to work cross-functionally and manage multiple priorities.

Responsibilities

• Supervise/Manage day-to-day Validation activities in accordance with approved Validation SOPs / Plan / Policies.
• Participate in the review and approve of Validation SOPs / Plans to facilitate the implementation of the Validation Strategy defined by the Validation Master Plan.
• Manage internal and external validation resources deployment to achieve department / project goals
• Liaise with system owner, quality unit and relevant departments including clients to ensure scope, execution and reporting of Validation Program meets their expectations
• Plan & manage on-job training program for staff. Perform regular review of department training requirements; identify gaps & improvements.
• Participate as required in regulatory inspections and client audits and responding to validation related issues.
• Plan, schedule, and manage, the validation efforts for large scale change implementation project in accordance with current Good Manufacturing Practices (cGMPs).
• Provide oversight for validation deviation investigation to resolve execution or result discrepancies and participate in the resolution of deviations and corrective/preventive actions.

Skills

People management

Cross-functional collaboration

Problem-solving

Analytical skills

Education

Degree in Engineering or Life Science or related discipline

Job description

Lonza Singapore Tuas is seeking an Associate Manager, Engineering - Validation to lead the validation lifecycle for facilities, equipment and utilities, ensuring regulatory compliance. This on-site role provides leadership over routine validation activities and supports real-time collaboration to maintain high quality and safety in medicines manufacturing.

Based in Singapore, you will supervise day-to-day validation tasks, review SOPs and plans, manage internal and external resources, train