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zer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It
The Senior QC Laboratory Analyst is to support the operation of Reference Standards Program. The incumbent is accountable for:
Meeting Key Performance Indices for Reference Standard program
Completing certification/recertification of reference standards in a timely manner
Complying to safety and cGMP policies, procedures and guideline
General responsibilities include
Conduct analytical testing
Conduct equipment training
Troubleshoot and rectify technical issues pertaining to equipment and tests
Calibrate/maintain equipment assigned
Maintain good house-keeping and safe working enviroment
Maintain/manage general lab inventory (e.g. Reference Standard, Chemical or Consumable Inventory)
Detect and report deviation, questionable/out of specification, safety concern
Participate in laboratory/safety investigations
Participate/lead in equipment qualification
Write/revise procedures, user guide
Guide junior analyst
Participate in assigned committees (e.g. Safety committee, License holder, etc)
Participate/lead in projects
Participate in internal/external audits
Perform peer review for solutions prepared in the laboratory
Qualifications
Diploma/Degree in Chemistry, Pharmacy or related fields.
Must-Have
Minimum 1 year relevant laboratory working experience, experience in similar field will be an added advantage.
Familiar with cGMP and ALCOA.
Knowledge in Microsoft office (such as Excel, Word, Teams).
Knowledge in analytical instrument and Empower 3 will be an added advantage
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Quality Assurance and Control
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