CQV Engineer / Senior, Clean Utilities

wuxi biologics biopharmaceuticals singapore private limited; Singapore; On-site; SGD 90,000 - 150,000; Full time

Job summary

WuXi Biologics in Singapore seeks a qualified professional to lead facility and utility qualification/validation activities, focusing on PW/WFI and clean gas systems. The role requires hands-on experience in cGMP environments and a strong grounding in QA practices.

You will review CQV deliverables, support vendor management, and ensure adherence to FDA/EMA standards and ISPE/PDA guidance, while maintaining safety and regulatory compliance.

Qualifications

• Bachelor degree or above, preferably in Engineering, Mechanical Engineering, Pharmaceutical Engineering, Automation, HVAC, Chemical Engineering, or related fields.
• 5–8 years of validation or QA experience in cGMP environments in biopharma.
• Experience with start-up facilities is preferred.
• Familiar with PW/WFI/Clean Steam processes and system design.
• Knowledge of regulatory requirements (FDA, EMA) and ISPE/PDA standards.
• Strong risk-based commissioning/qualification experience (URS, DQ, FAT, SAT, IQ, OQ, PQ).
• Understanding of Quality System and EHS requirements.

Responsibilities

• Participate in qualification/validation of facility, utilities and equipment, focusing on clean utilities (PW/WFI/PS systems and clean process gases).
• Review C&Q deliverables from internal teams or equipment suppliers; develop C&Q documents as needed.
• Participate in qualification execution.
• Address validation variances and change control assessments in the project phase.
• Support C&Q service provider management and ensure SOP adherence.
• Assist in developing and implementing C&Q plans aligned with project timelines; track deliverables to meet timelines.
• Complete trainings per the training plan.
• Ensure compliance with regulatory requirements and WuXi Biologics standards and EHS.

Skills

Interpersonal communication

Verbal communication

Written communication

Critical thinking

Problem solving

Attention to detail

Self-motivation

Adaptability

Education

Bachelor degree or above in Engineering/related fields

Job description

WuXi Biologics is a premier provider of biologics services (from discovery to commercialization) with global customers in the biopharmaceutical and healthcare industries. We´re one of the world's top three contract development and manufacturing companies for biopharmaceuticals, we provide our clients with a world-leading open access technology platform. We enable our clients to research, develop and manufacture drugs from the concept phase to commercial manufacturing.

Our mission is to accelerate and transform discovery, development, and manufacturing in the rapidly growing field of biologics to benefit patients worldwide. We have sites/offices in China, the US, the EU, and Asia. We currently employ over 10,000 people and provide services to more than 600 customers worldwide, including the top 20 biopharmaceutical companies.

Department Description

GENG is responsible for capital and expansion construction projects per the Company's business strategic plan, and carry out all-round and whole-process project construction management, including due diligence report, design, civil, MEP and CQV, until delivering the biopharmaceutical R & D and GMP facilities to meet different needs; also providing business in terms of procurement, civil, MEP and CQV for external customers.

Your Responsibilities

• Responsible for participating qualification/validation of facility, utility and equipment, mainly for clean utilities which include PW/WFI/PS systems and clean process gases system (compressed air, O₂, N₂, CO₂);

• Review C&Q deliverables, either from internal or from equipment suppliers / C&Q service providers, develop C&Q documents if required;

• Participate in qualification execution;

• Participate in resolution of validation variance, change control assessment occurred in the project phase;

• Participate in validation C&Q service provider management, provide guidance on company SOP requirement to vendors;

• Support the development and implementation of C&Q plans aligned with project timelines, track the C&Q deliverables and activities to meet project timelines.

• Complete trainings timely according to company training plan.

• Ensure compliance with appropriate regulatory requirements and WuXi Biologics requirements, and follow all EHS requirements.

Requirement:

• Bachelor degree or above, preferably in Engineering, Mechanical Engineering, Pharmaceutical Engineering, Automation, HVAC, Chemical Engineering, or related fields.

• 5 - 8 years of experience in validation or QA related work experience in cGMP environment or pharmaceutical/biopharmaceutical company.

• Demonstrated experience in start-up facilities is preferred.

• Familiar with one or more of the following systems: Purified Water (PW) / Water for Injection (WFI)/ Clean Steam include the process, system design.

• Good knowledge and experience of regulatory requirements (FDA, EMA) and industry standards (ISPE, PDA).

• Strong understanding of risk-based approaches to commissioning and qualification/validation, Hand-on experience with qualification/validation lifecycle (URS, DQ, FAT, SAT, IQ, OQ, PQ) for clean utilities.

• Good understanding of Quality System, EHS.

• Excellent interpersonal, verbal, and written communication skills

• Able to think critically and demonstrate troubleshooting and problem-solving skills

• Self-starter and self-motivated; organized with good attention to detail

• Comfortable working in a fast-paced environment and able to adjust workloads based on changing priorities