CQV, Validation & Quality Consultant (Hybrid Profile)

CQV, Validation & Quality Consultant (Hybride Profile) | Singapore

We are seeking a highly versatile CQV, Validation & Quality Consultant (Hybrid Profile) to join our team in Singapore. As a key member, you will deliver end-to-end support for commissioning, qualification, validation, and quality assurance activities across pharma, biotech, and medical device projects.

Your Responsibilities:

• Lead and execute Commissioning, Qualification & Validation (CQV) activities for equipment, utilities, facilities, and computerized systems (CSV)
• Develop, review, and execute validation protocols (DQ, IQ, OQ, PQ), cleaning and process validation
• Prepare and optimize Quality Assurance documents (SOPs, technical reports, risk assessments)
• Support regulatory compliance with GMP, FDA, EMA, PIC/S, and HSA Singapore standards
• Manage and support client audits, regulatory inspections, and remediation actions
• Collaborate with engineering, QA, and digital teams to ensure successful project delivery
• Advise on data integrity and participate in digital transformation/validation projects
• Provide technical expertise and training to client teams

Your Profile:

• Bachelor's or Master's degree in Engineering, Life Sciences, Pharmacy or related field
• Minimum 3 years experience in CQV, validation and quality roles within pharmaceutical, biotech, or medical device environments
• Solid knowledge of GMP, regulatory requirements, quality systems, and validation protocols
• Proven hands-on experience with equipment/utilities qualification and CSV
• Strong documentation, problem-solving, and communication skills in English
• Adaptable, collaborative, and proactive mindset; able to manage multiple projects
• Experience in Singapore/Asia-Pacific region is an advantage

Apply now and join a dynamic international team !