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Interested applicants please write in to contact person at the bottom of the email.
QC Laboratory Analyst
The Incumbent is a member of the Quality Control (QC) Laboratory team. Under the supervision of the QC Laboratory Supervisor, the incumbent will be responsible for performing all analytical testing and the review of the test results generated. This is accomplished by following site procedures and approved test methods and assisting in troubleshooting laboratory technical problems and support laboratory investigation. In addition to analytical testing responsibilities perform preventive maintenance or calibration of instrumentation as required and undertake housekeeping responsibilities and follow safety regulations.
Responsibilities:
o Perform analytical testing accurately and efficiently and in accordance to Standard Operating Procedures (SOPs).
o Perform equipment verification and calibration in accordance to procedures.
o Document all results in accordance to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) requirements.
o Ensure all quality records are attached and/or file as predetermined.
o Practice laboratory good housekeeping and ensure all safety procedures are followed.
o Conduct training to fellow colleagues on simple procedures (hygiene and safety)
o Participate actively and contribute to site project teams.
o Contribute to the continuous improvements in laboratory activities.
o Highlight abnormality during testing and obtain authorization for laboratory investigation from supervisor.
o For more experienced analyst, to mentor new colleagues as required
o Perform equipment troubleshooting where required.
o Track trending of data as part of proactive monitoring.
Accountabilities:
o Analytical testing and review of test results to meet lead time in a right first time manner; § Perform testing according to Standard Work Plan (SWP) as assigned.
§ Ensure training records are updated and promptly, are correctly filed to reflect current testing capabilities.
o Equipment verification and calibration accordance to site or pharmacopeia standards and according to schedule; § Ensure instrumentation is calibrated / maintained in accordance to schedule as required.
§ Update relevant instrument SOPs as required to ensure it reflects current requirement and practice.
o Compliance to GMP/GLP and Pfizer Quality Standards (PQS) requirements; § Follow approved SOPs.
§ Understand and comply with Data Integrity and Good Documentation Practices (GDP) requirements.
o Laboratory safety and housekeeping; § Contribute to and participate in laboratory housekeeping and 5S program responsibilities.
§ Wear Personal Protective Equipment (PPE) as required and observe safety instructions stated in Job Safety Analysis (JSAs), Standard Test Methods (STPs) and Material Application Document (MADs).
Diploma in Science or Chemical Process Technology
For a Senior QC Laboratory Analyst: A minimum of 3 years QC experience in the pharmaceutical industry.
For A QC Laboratory Analyst: A minimum of 1 years QC experience in an analytical laboratory.
Flexi Work - Tuas (Singapore)
A career at Pfizer offers opportunity, ownership and impact.
All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the bio-pharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
For interested applicants, please email your CV/resume to Ms Hoe (yee_hoe@hotmail.com).
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