CQV Engineer (Aseptic/ Sterile) - Growth & Benefits

No deviation Pte Ltd.; Singapore; Hybrid; SGD 90,000 - 130,000; Full time

Benefits offered by this job

Generous leave policy

Health & wellness coverage

Professional development opportunities

Job summary

No deviation Pte Ltd. is seeking a CQV Engineer with strong aseptic/sterile manufacturing experience to execute commissioning, qualification, and validation activities across equipment, utilities, and cleanrooms.

The role requires compliance with GMP and regulatory requirements and close collaboration with QA, Engineering, and Production to ensure project success. The ideal candidate will have 3–5 years in CQV within pharma/biotech, hands-on aseptic experience, and a proven track record in

Qualifications

• Bachelor's Degree in Engineering, Life Sciences, or related discipline.
• 3–5 years of CQV experience within pharmaceutical or biotechnology industries.
• Hands-on experience in aseptic or sterile manufacturing environments.

Responsibilities

• Execute IQ/OQ/PQ for process equipment, clean utilities, and facilities in aseptic areas.
• Develop, review, and approve validation protocols and reports per GMP, FDA, EU guidelines.
• Support aseptic processes, including cleanroom qualification, HVAC, and environmental monitoring.

Education

Bachelor's Degree in Engineering, Life Sciences, or related discipline

Job description

No deviation Pte Ltd. is seeking a CQV Engineer with strong aseptic/sterile manufacturing experience to execute commissioning, qualification, and validation activities across equipment, utilities, and cleanrooms.

The role requires compliance with GMP and regulatory requirements and close collaboration with QA, Engineering, and Production to ensure project success. The ideal candidate will have 3–5 years in CQV within pharma/biotech, hands-on aseptic experience, and a proven track record in