Validation Manager (Design Transfer) 12 months contract

PERSOL; Singapore; On-site; SGD 120,000 - 180,000; Full time

Job summary

PERSOL seeks an experienced Validation Manager (Design Transfer) to lead validation activities in a regulated manufacturing environment in Singapore. The role covers planning, executing, and documenting validation for facilities, equipment, utilities, processes, and computerized systems to ensure cGMP, cGDP, and ALCOA+ data integrity.

You will review validation protocols and reports, coordinate with cross-functional teams, and support regulatory inspections and audits, driving timely project

Qualifications

• Bachelor's degree in Engineering, Science, or a related discipline.
• Minimum 10 years of hands-on validation experience in a regulated industry (pharmaceuticals/biotech/medical devices).
• Strong experience in qualification and validation of facilities, equipment, utilities, manufacturing and cleaning processes, and computerized systems.
• Solid understanding of regulatory requirements, validation methodologies, and quality systems.
• Knowledge of cGMP, cGDP, ALCOA+ Data Integrity Principles.
• Excellent communication, interpersonal, and stakeholder management skills.

Responsibilities

• Support design transfer activities, including validation and qualification of facilities, equipment, utilities, materials, manufacturing processes, cleaning processes, and computerized systems.
• Ensure all validation activities are appropriately planned, executed, documented, and completed in compliance with regulatory requirements and internal SOPs.
• Review and approve validation protocols, reports, and supporting documentation to ensure accuracy, completeness, and regulatory compliance.
• Coordinate with cross-functional stakeholders to support project timelines and validation deliverables.
• Maintain accurate and organized validation records to support regulatory inspections, audits, and quality system requirements.
• Investigate validation-related issues and support the implementation of corrective and preventive actions where required.
• Ensure compliance with cGMP, cGDP, and ALCOA+ data integrity principles.

Skills

Communication skills

Interpersonal skills

Stakeholder management

Analytical and problem solving

Education

Bachelor's degree in Engineering, Science or related field

Job description

About the role

We are seeking an experienced Validation Manager (Design Transfer) to support design transfer and validation activities within a highly regulated manufacturing environment. The successful candidate will be responsible for planning, executing, reviewing, and documenting validation activities to ensure compliance with regulatory requirements, company quality standards, and internal Standard Operating Procedures (SOPs).

Key responsibilities

• Support design transfer activities, including validation and qualification of facilities, equipment, utilities, materials, manufacturing processes, cleaning processes, and computerized systems

• Ensure all validation activities are appropriately planned, executed, documented, and completed in compliance with regulatory requirements and internal SOPs

• Review and approve validation protocols, reports, and supporting documentation to ensure accuracy, completeness, and regulatory compliance

• Coordinate with cross-functional stakeholders to support project timelines and validation deliverables

• Maintain accurate and organized validation records to support regulatory inspections, audits, and quality system requirements

• Investigate validation-related issues and support the implementation of corrective and preventive actions where required

• Ensure compliance with current Good Manufacturing Practices (cGMP), Good Documentation Practices (cGDP), and ALCOA+ data integrity principles

About you

• Bachelor's Degree in Engineering, Science, or a related discipline

• Minimum 10 years of hands-on experience in validation within the pharmaceutical, medical device, biotechnology, or related regulated industry

• Strong experience in qualification and validation of facilities, equipment, utilities, manufacturing processes, cleaning processes, and computerized systems

• Good understanding of regulatory requirements, validation methodologies, and quality systems

• Knowledge of cGMP, cGDP, ALCOA+ Data Integrity Principles

• Strong communication, interpersonal, and stakeholder management skills

• Excellent analytical and problem-solving abilities

• Ability to prioritize tasks and work effectively within project timelines

• Experience supporting design transfer or technology transfer projects (preferred)

• Experience managing regulatory inspections and internal/external audits (preferred)