Why Patients Need YouEverything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.
Why Patients Need YouEverything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.
What You Will AchieveYour prior work experience and ability to apply your breadth of knowledge will help you adapt the standard methods and procedures. You will help us identify required delivery and process improvements that drive increased efficiency, throughput and quality. You will arrive at decisions on which methods and procedures are the best fit for different work situations.It is your hard work and commitment that will make Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve ItThe 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
QualificationsDiploma/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#LI-PFE