CQV Consultant

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 !