CQV Project Engineer - Validation & Commissioning Lead

Anter Consulting Pte. Ltd

Singapore

On-site

SGD 75,000 - 95,000

Full time

14 days+

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Job summary

Anter Consulting Pte. Ltd in Singapore is looking for a skilled professional to lead commissioning, qualification, and validation (CQV) activities for various projects. The ideal candidate will manage project timelines, coordinate with cross-functional teams, and ensure compliance with GMP standards.

Applicants should have a Bachelor's degree in Engineering and 5-7 years of relevant experience in the pharmaceutical or biotech sector. This is a great opportunity to drive impactful projects within a dynamic team.

Qualifications

  • Bachelor's degree in Engineering or a related field.
  • 5-7 years of experience in CQV, validation, and commissioning, preferably in pharmaceutical or biotech.
  • Strong understanding of GMP standards and regulatory compliance.
  • Proven ability to manage multiple projects and priorities effectively.
  • Excellent problem-solving and communication skills.

Responsibilities

  • Lead and support commissioning, qualification, and validation activities for assigned projects.
  • Manage project timelines, ensuring deliverables are met within scope, budget, and regulatory compliance.
  • Develop and execute validation protocols for equipment and systems.
  • Coordinate with cross-functional teams for seamless project execution.
  • Identify and resolve technical issues during commissioning and qualification phases.
  • Support continuous improvement initiatives to optimize processes.

Skills

CQV processes
GMP standards
Project management
Problem-solving
Communication skills

Education

Bachelor's degree in Engineering or related field

Job description

Anter Consulting Pte. Ltd in Singapore is looking for a skilled professional to lead commissioning, qualification, and validation (CQV) activities for various projects. The ideal candidate will manage project timelines, coordinate with cross-functional teams, and ensure compliance with GMP standards.

Applicants should have a Bachelor's degree in Engineering and 5-7 years of relevant experience in the pharmaceutical or biotech sector. This is a great opportunity to drive impactful projects within a dynamic team.

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