CQV Lead Jobs in Singapore

    CQV Lead

      ஆலோசகர்:
      வேலை குறிப்பு எண்.
      TZ34998
      பதிவு எண்.
      R1439740
      உரிமம் எண்.
      16S8060
      செயல்பாடு
      பொறியியல்
      தொழில்
      உடல்நலம் & வாழ்க்கை அறிவியல்

      CQV Lead

      Our client, a globally recognized manufacturer in the Life Science sector, is seeking a seasoned professional to join their Singapore Programme as a CQV Lead. This is a unique opportunity to contribute to a next-generation facility designed for long-term scalability and innovation.

      This role offers the chance to play a pivotal role in a high-impact capital project, working alongside multidisciplinary teams in a fast-paced and purpose-driven environment.

      Key Responsibilities:

      • Lead the planning and execution of commissioning, qualification, and validation (CQV) activities across process equipment, utilities, cleanroom environments, automation platforms, and supporting infrastructure.
      • Collaborate closely with engineering, MEP, automation, quality, supply chain, and operations teams to ensure alignment with project objectives and regulatory expectations.
      • Develop and implement FAT, SAT, IQ, OQ, and PQ protocols, ensuring technical governance and compliance with global quality frameworks.
      • Oversee system turnover from EPCM partners to operations, maintaining documentation integrity, traceability, and adherence to project timelines.
      • Drive risk mitigation strategies and ensure compliance with validation master plans, GMP standards, and global engineering guidelines.
      • Provide leadership and mentorship to CQV teams, fostering high-quality execution and operational excellence.
      • Support governance and reporting processes by delivering key performance insights and milestone updates to senior stakeholders.

      Requirements:

      • Degree in Engineering (Chemical, Mechanical, Electrical, or related discipline) or equivalent.
      • Minimum of 10-12 years’ relevant experience in CQV within biopharmaceutical, high-tech, or advanced manufacturing environments.
      • Proven track record in leading CQV activities for GMP-regulated facilities, including greenfield or major capital projects.
      • Strong understanding of automated systems, critical utilities, and process technologies.
      • Demonstrated leadership, stakeholder engagement, and strategic planning capabilities.
      • Proactive, hands-on, and results-driven, with the ability to manage multiple priorities in a dynamic environment.

      To Apply:

      Please submit your resume in Word or PDF format to Tahmid Bin Zafar at tahmid@kerryconsulting.com, quoting the job title and reference no TZ34998. We regret that only shortlisted candidates will be notified.

      License No: 16S8060
      Registration No: R1439740

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