Validation Engineer

Our esteemed client, an established MNC, is searching for a Validation Engineer:

Job Responsibilities:

Execute commissioning, qualification, and validation (CQV) activities for GMP-regulated pharmaceutical and biopharmaceutical facilities.
Prepare and review validation documentation, including Validation Plans, IQ/OQ/PQ protocols, test scripts, and final reports.
Support the validation of equipment, utilities, facilities, and computerized systems in compliance with GMP, GAMP 5, and 21 CFR Part 11 requirements.
Coordinate with project engineers, QA teams, clients, and vendors to ensure timely completion of validation deliverables.
Conduct risk assessments, impact assessments, and deviation investigations, and implement appropriate CAPA.
Ensure all validation activities comply with applicable regulatory requirements and company quality standards.
Support FAT, SAT, commissioning, and qualification activities for new equipment and systems.
Maintain accurate documentation and ensure data integrity throughout the validation lifecycle.

Job Requirements:

Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a related discipline.
3–5 years of relevant validation/CQV experience in the pharmaceutical or biopharmaceutical industry.
Good knowledge of GMP, GAMP 5, FDA 21 CFR Part 11, EU GMP, and data integrity requirements.
Experience with equipment, utilities, cleanrooms, HVAC, water systems, or computerized system validation is preferred.
Strong documentation, analytical, and problem-solving skills.
Good communication skills with the ability to work effectively in a multidisciplinary project environment.

Additional Information:

For interested parties, kindly click on "APPLY NOW" or send in your resume in MS Word format to

applicant@tstar-recruit.com.sg

*We regret that only shortlisted candidates will be notified*

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