- Islandwide (Singapore) Singapore

Working Location
Job Description
Responsibilities
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.
Important Information
Never provide your bank or credit card details when applying for jobs. Do not transfer any money or complete unrelated online surveys. If you see something suspicious, Report this Job ad.