CQV Engineer: Commissioning & Validation Specialist

PSC Biotech® Corporation; Singapore; On-site; SGD 70,000 - 110,000; Full time

Job summary

PSC Biotech Corporation is seeking a mid-level CQV Engineer to join its team in Singapore. The role involves authoring, reviewing and approving validation documents, and ensuring compliance with regulatory and quality standards across GxP systems.

The ideal candidate will have a degree in Chemical/Biomedical Engineering, strong communication skills, and experience in the Life Sciences industry. Travel or relocation is preferred but not required.

Qualifications

• Bachelor’s degree in Chemical Engineering, Biomedical Engineering, or related field.
• Proven experience in Life Sciences and GxP industries.
• Must have strong written and verbal communication skills.
• Willingness to travel or relocate (preferred).

Responsibilities

• Provide CQV authoring, review and approval of validation documents.
• Initiate/update GxP and Risk Assessments on system.
• Draft and execute validation documentation.
• IQ and OQ Test Scripts; IQ/OQ/PQ Protocols as necessary.
• Translate system requirement specifications into executable validation protocols.
• Collaborate with project stakeholders and IT to define needs and solutions.
• Maintain Traceability Matrix (TMX) and Validation Summary Reports.

Skills

CQV engineering

Regulatory knowledge

Documentation skills

Stakeholder collaboration

Analytical thinking

Time management

Education

Chemical/Biomedical Eng

Job description

PSC Biotech Corporation is seeking a mid-level CQV Engineer to join its team in Singapore. The role involves authoring, reviewing and approving validation documents, and ensuring compliance with regulatory and quality standards across GxP systems.

The ideal candidate will have a degree in Chemical/Biomedical Engineering, strong communication skills, and experience in the Life Sciences industry. Travel or relocation is preferred but not required.