A
Advanced Manufacturing Tech Solutions
Validation Engineer - Cleaning and Validation
Skills
Testing & QACompliance
2 months ago
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Important information
Contract type:
Permanent
Location:
Singapore
Work mode:
Onsite
Published on:
7 August 2026
What they need
Validation Engineer – Cleaning Validation Location: Singapore, Tuas.
Industry: Pharmaceutical Manufacturing | Life Sciences
Key Responsibilities
- Support execution of Cleaning Validation activities for GMP manufacturing equipment and process systems.
- Develop, review, and execute Cleaning Validation protocols and reports.
- Support cleaning validation lifecycle activities in accordance with site procedures and regulatory requirements.
- Define and evaluate cleaning acceptance criteria and residue limits.
- Support product-to-product changeover assessments and cleaning verification strategies.
- Perform and review swab and rinse sampling activities.
- Evaluate cleaning validation data and prepare technical summary reports.
- Participate in risk assessments related to cleaning validation activities.
- Support investigations related to cleaning validation deviations, CAPAs, and change controls.
- Collaborate with Manufacturing, MSAT, Engineering, QA, QC, and Validation teams to ensure successful execution of validation activities.
- Ensure compliance with GMP, Data Integrity, and applicable regulatory guidelines.
- Support inspection readiness and audit activities.
Requirements
- Degree in Engineering, Biotechnology, Pharmaceutical Sciences, Chemistry, Life Sciences, or related discipline.
- Experience in Cleaning Validation within pharmaceutical, biotechnology, or GMP-regulated manufacturing environments.
- Strong understanding of Cleaning Validation lifecycle principles and methodologies.
- Experience developing, executing, and reviewing Cleaning Validation protocols and reports.
- Knowledge of residue limit calculations, acceptance criteria, and risk-based validation approaches.
- Familiarity with swab recovery studies, rinse sampling, and cleaning verification practices.
- Understanding of GMP regulations, Data Integrity requirements, and validation compliance expectations.
- Experience supporting deviation investigations, CAPA implementation, and change control processes.
- Strong technical writing, documentation, and report preparation skills.
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