About this role
Responsibilities: • Coordinate the routine PM, Cal and ad-hoc repair of equipment (fridges, freezers, stability chambers, incubators, ovens, isolators, etc) with corresponding vendors. • Collaborate with field service engineers to troubleshoot equipment issues and ensure equipment remain in a qualified state after repairs, software updates, or relocation. • Generate comprehensive and audit-ready documentation for all GMP activities, ensuring compliance. • Conduct checks to verify equipment functions according to manufacturer specifications and user requirements. • 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 equipment maintenance. • Manage equipment alarms timely and determine root cause of alarms. • Analyze alarm trends and take proactive actions to maintain equipment in healthy state. 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: 6 months, subject to renewal based on performance
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