Commissioning, Qualification and Validation Engineer

Wood
Singapore
Workplace: OnsiteFull timeFunction: OtherExperience: 3+ yearsEducation: bachelorsSkills: []

CQV Engineer for life science projects in Singapore. Responsible for commissioning, qualification, and validation of equipment, systems, and processes in pharmaceutical plants, ensuring GMP compliance and audit-ready documentation. Work with cross-functional teams to optimize operations, conduct risk assessments, and execute IQ/OQ/PQ protocols while supporting regulatory inspections and continuous improvement.

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Wood
Wood
4 months ago

Commissioning, Qualification and Validation Engineer

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Last checked: 4 hours agoStatus: Live

Job Summary

CQV Engineer for life science projects in Singapore. Responsible for commissioning, qualification, and validation of equipment, systems, and processes in pharmaceutical plants, ensuring GMP compliance and audit-ready documentation. Work with cross-functional teams to optimize operations, conduct risk assessments, and execute IQ/OQ/PQ protocols while supporting regulatory inspections and continuous improvement.
Location: Singapore
Workplace: Onsite
Employment Type: Full time
Seniority: Mid level

Key Responsibilities

  • •Commissioning activities for new and existing equipment and systems; develop and execute commissioning plans, protocols, and reports; coordinate with cross-functional teams to ensure smooth equipment startup and integration.
  • •Lead qualification efforts for equipment, utilities, and facilities; develop and implement qualification protocols (IQ, OQ, PQ); conduct risk assessments and ensure proper documentation of qualification activities.
  • •Manage validation processes for manufacturing processes, cleaning procedures, and computer systems; create and execute validation plans, protocols, and reports; ensure GMP compliance.
  • •Documentation: maintain comprehensive and accurate documentation of commissioning, qualification, and validation activities; ensure documentation is audit-ready.
  • •Compliance: stay updated on industry regulations and guidelines related to CQV; ensure activities are performed in compliance with FDA, EMA and internal quality standards.

Key Requirements

  • •Bachelor’s degree in Engineering, Life Sciences, or a related field.
  • •Certification in CQV or related areas, will be added advantage.
  • •Strong knowledge of GMP, FDA, and EMA regulations, and experience in regulatory inspections and audits.
  • •Proficiency in using validation software and tools.
  • •Minimum 3 years of experience in commissioning, qualification, and validation within the pharmaceutical industry.
Experience:3+ yearsLife sciencePharmaceuticalPharmaGMP
Education:Bachelor's
Certifications:CQV
Tech Stack:IQOQPQValidation softwareRegulatory inspectionsValidation protocols

Company Brief

Wood
Provides engineering, project delivery and technical consultancy services across energy, built environment and industrial sectors, delivering integrated solutions for oil & gas, renewables, infrastructure and environmental projects worldwide.
Industry: Consulting
Company Size: Enterprise (1,001+ employees)
Revenue: USD 1B+
Growth: Public Company
Valuation: Public Company (Market Cap in USD)
Funding: IPO / Publicly Listed
Headquarters: Aberdeen, United Kingdom
Founded: 1982
WebsiteLinkedIn