1 year contract
Located in Tuas
Paying up to $5500
about the company
A leading global biopharmaceutical manufacturer known for technical excellence and high-quality production standards.
about the job
Drive operational success and process integrity across large-scale manufacturing campaigns in a state-of-the-art facility.
- Lead root cause investigations for operational deviations, non-conformities, and floor abnormalities using structured methodologies.
- Facilitate cross-functional technical alignment with subject matter experts and quality teams to establish root causes and design effective corrective actions.
- Conduct comprehensive product quality impact assessments to support timely lot disposition and release activities.
- Prepare end-to-end investigation reports detailing technical findings, impacted batches, and preventive action effectiveness.
- Support operational readiness and run activities including batch record updates, change requests, and material management.
skills and experience required.
- Strong background in leading deviation investigations and root cause analysis within the pharmaceutical or biopharmaceutical industry.
- Proficiency in structured investigation tools such as 5 Whys, Fishbone diagrams, Causal Branching, or FMECA.
- Proven track record in assessing product quality impact and managing corrective and preventive action programs.
- Practical experience supporting operational readiness, process campaigns, and technical documentation creation.
- Excellent technical writing capabilities and experience presenting investigation outcomes to internal and external stakeholders.
Please click on the 'apply' button to apply online. For more information, please reach out to Wai Ling Tai. (EA: 94C3609 / R1110392 )
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