Commissioning, Qualification and Validation Manager

As a CQV Engineer, you will be responsible for ensuring the successful commissioning, qualification, and validation of equipment, systems, and processes within client’s pharmaceutical plant. You will play a crucial role in maintaining compliance with industry regulations, optimizing operational efficiency, and ensuring the quality and safety of the...

Remarkable people, trusted by clients to design and advance the world.Wood is currently recruiting for a Commissioning, Qualification and Validation Engineer to support our growing operations in Singapore. You will be responsible for the execution of project work in accordance with company procedures within the man-hour and cost budgets.#LI-OnsiteThe RoleAs...

Principal Commissioning Qualification & Validation Engineer Join to apply for the Principal Commissioning Qualification & Validation Engineer role at Wood . As a CQV Engineer, you will be responsible for ensuring the successful commissioning, qualification, and validation of equipment, systems, and processes within client’s pharmaceutical plant. You will...

**Permanent Role**: - **Basic Salary Up to 7,000 + 2 months VB**: - **Working location: West MRT**: - **Pharmaceutical Industry Experience is a MUST**: - **CIP, SIP experiences will be preferred** **Responsibilities**: - Perform risk-based commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on Process...

Responsibilities: _ - Provide direct services to site Technical Services management, contributing to increased throughput of commissioning and qualification activities across the site. - Collaborate with Technical Services management while independently performing required validation activities. - Support C&Q activities across the site as directed by site...

**Previous Pharmaceutical/Biotech experience is mandatory for this role.** MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical, and biotechnology industries. Its services include Engineering, Project Management, and Validation. MMR has offices in Canada, USA, Australia, Singapore and India. **Responsibilities** - Provide...

Job Description - Permanent Role - Basic Salary range from $4000 to $7,000 + 2 months VB - Pharmaceutical Industry Experience is a MUST **Responsibilities**: - Perform risk-based commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on Process Equipment, CIP / SIP, Process Manufacturing and related business...

PM Singapore is currently looking to expand the CQV capabilities. This role will be supporting one of our many clients in the field of commissioning, qualification and validation work within the Life Sciences space. Your day to day role would involve the following activities: Planning, Performance, and Coordination of Computer System Validation,...

Job Description - Permanent Role - Up to $7,500 + 2 months VB - Working location: West MRT - Pharmaceutical Industry Experience is a MUST - CIP, SIP experiences will be preferred **Responsibilities**: - Perform risk-based commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on Process Equipment, CIP / SIP,...

Responsibilities: Plan, execute, and manage commissioning, qualification, and validation (CQV) activities for pharmaceutical/biotech manufacturing facilities, utilities, and process equipment. Develop and review CQV protocols (IQ/OQ/PQ) and reports in compliance with GMP, GAMP 5, and company procedures. Coordinate with engineering, project, and quality...