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Scientist (Instrument Qualification)

External
S$54K–S$78K/yrContractUnknown1w ago
ComplianceDocumentation
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About the role

Main Responsibilities: ●Develop and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols for new and existing analytical instruments. ●Generate comprehensive and audit-ready documentation for all qualification activities, ensuring compliance. ●Conduct tests to verify that instruments function according to manufacturer specifications and user requirements, analyzing the resulting data to confirm accuracy, precision, and linearity. ●Collaborate with field service engineers and lab personnel to troubleshoot equipment issues and ensure instruments remain in a qualified state after repairs, software updates, or relocation. ●Train laboratory staff on the proper use of qualified equipment and associated standard operating procedures (SOPs). ●Support internal and external audits by providing documentation and technical expertise related to instrument qualification. About You: ● Bachelor degree in a relevant scientific field (e.g., Chemistry, Biology, Biomedical Engineering, or related discipline). ● Min 3 years of relevant experience in pharma or biotech facilities. ●Knowledge of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) in a pharma or biotech facility ● Good interpersonal, communication and presentation skills. ●Must be a self-starter, fast learner, curious with strong analytical and organizational skills ● Self-motivated and willingness to learn ●Reliable and Responsible Contract Duration: 12 months, subject to renewal based on performance.


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