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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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