Validation Manager (Design Transfer & Qualification) 12 months contract

PERSOL SINGAPORE PTE. LTD.; Singapore; On-site; SGD 78,000 - 112,000; Full time

Job summary

PERSOL SINGAPORE PTE. LTD. is seeking an experienced Validation Manager to lead validation activities in a regulated manufacturing setting.

This role focuses on planning, executing and documenting qualification efforts across facilities, equipment, utilities, processes, and computerized systems. The ideal candidate has 10+ years of hands-on validation experience in pharmaceutical, medical device or biotech sectors, with strong knowledge of cGMP, cGDP and ALCOA+ data integrity principles and

Qualifications

• Bachelor's Degree in Engineering, Science, or a related discipline.
• Minimum 10 years of hands-on validation experience in regulated industries.
• Experience in qualification/validation of facilities, equipment, utilities, processes and computerized systems.
• Knowledge of regulatory requirements and quality systems.
• Familiarity with cGMP, cGDP and ALCOA+ principles.

Responsibilities

• Support design transfer activities including validation and qualification across facilities, equipment, utilities, manufacturing processes and computerized systems.
• Ensure validation activities are planned, executed, documented and compliant with regulatory requirements and SOPs.
• Review and approve validation protocols, reports and supporting documents for accuracy and compliance.
• Coordinate with cross-functional stakeholders to meet project timelines and validation deliverables.
• Maintain organized validation records for inspections, audits and quality systems.
• Investigate validation-related issues and support CAPA implementation.

Skills

Validation

GxP compliance

cGMP

cGDP

ALCOA+ Data Integrity

Stakeholder management

Analytical thinking

Project prioritization

Quality systems

Strong communication

Education

Bachelor's Degree in Engineering/Science or related

Tools

Validation software

QMS systems

Job description

About the Role

We are seeking an experienced Validation Manager 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).

This is an excellent opportunity for a seasoned validation professional with strong hands-on experience in qualification and validation activities across facilities, equipment, manufacturing processes, and computerized systems.

Key Responsibilities

• Support design transfer activities, including validation and qualification of:
• Facilities
• Equipment
• Utilities
• Materials
• Manufacturing processes
• Cleaning processes
• 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.

Requirements

• 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.

Preferred Qualifications

• Experience supporting design transfer or technology transfer projects.
• Experience managing regulatory inspections and internal/external audits.
• Familiarity with validation lifecycle management and risk-based validation approaches.

Why Join Us?

Opportunity to work on impactful design transfer and validation projects.

Collaborative and quality-focused work environment.

Exposure to highly regulated pharmaceutical/medical device manufacturing operations.

Work alongside experienced cross-functional teams in engineering, quality, and operations.

Salary range : S$7,000.00 – S$10,000.00

Location : Downtown