Associate Manager, Engineering - Validation

Location: Fully site-based in Tuas, Singapore

Company

hirify.global operates more than 30 sites across five continents and manufactures medicines and life-science products through globally connected teams.

What you will do

• Manage daily facility, equipment, and utility validation activities according to approved validation SOPs, plans, and policies.
• Review and approve validation SOPs and plans supporting the strategy defined by the Validation Master Plan.
• Deploy internal and external validation resources to achieve department and project goals.
• Coordinate with system owners, the quality unit, relevant departments, and clients to align validation scope, execution, and reporting.
• Plan and manage staff on-the-job training, review training requirements, and identify gaps and improvements.
• Participate in regulatory inspections and client audits, manage validation deviations, and support corrective and preventive actions for large-scale change implementation projects under current Good Manufacturing Practices.

Requirements

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

Culture & Benefits

• Agile career environment and dynamic working culture.
• Inclusive and ethical workplace focused on collaboration, accountability, excellence, passion, integrity, and diversity.
• Compensation programs that recognize high performance.
• Benefits vary according to the role and location.
• Fully site-based work supports in-person collaboration and technical precision in medicine manufacturing.