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QC Chemist

Pfizer


Location:
Paso Robles, CA 93446
Date:
02/13/2018
2018-02-132018-03-16
Pfizer
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Job Details

Position Summary:







The incumbent is member of the Quality Control (QC) Laboratory team and is under the supervision of the QC Supervisor (System).







The incumbent will resume a new role in Tuas, Singapore to project manage data integrity assessment and remediation efforts in the short and long term, construct, exercise and continuously improve sustainable best practices for a data integrity program at the Tuas, Singapore site.







Incumbent shall have tactical skills in support of technical system risk management, as well as strategic capability in program development and ownership, work independently with minimal supervision.







Job Description:







+ Perform analytical and basic microbiological testing accurately and efficiently and in accordance to Standard Operating Procedures (SOPs).



+ Perform equipment verification and calibration in accordance to procedures.



+ Document all results in accordance to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) requirements.



+ Ensure all quality records are attached and/or file as predetermined.



+ Write and review Standard Operating Procedures (SOPs) and On the Job Training (OJTs) for the laboratory.



+ Conduct Laboratory investigations.



+ Perform maintenance and troubleshooting of laboratory equipment where required.



+ Perform equipment qualification and analytical method validation where required.



+ Perform laboratory equipment verification and calibration in accordance to procedures where required.



+ Perform basic microbiological testing such as endotoxin level in water and products.



+ Ensure all documentations and quality records are conducted in accordance to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) requirements and that they are filed in accordance to existing policies.



+ Participate actively and contribute to site project teams.



+ Train fellow colleagues on written procedures and SOPs pertaining to equipment operation, analytical and microbiological test methods and general laboratory operation.



+ Perform review and approval of test results in the Laboratory Information Management System (LIMS).



+ Perform proactive trending of analytical and microbiological test results.



+ Prepare analytical and microbiological for Annual Product Review Reports (APRR).







Accountability:







+ 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.



+ 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.



+ 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.



+ 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).







+ Equipment Qualification;



+ Perform IQ/OQ/PQ of new equipment with assistance from vendor.



+ Conduct preventive maintenance( internal) of equipment



+ Method validation;



+ Perform validation of /test methods in accordance to STP and USP/JP/EP requirements



+ Complete validation documents reports as required.



+ Procedures Development & Review;



+ Update SOPs to align with PQS and regulatory authority requirement (ICH guidelines)



+ Review the SOPs periodically to ensure they are current and represent current practice and align to latest PQS.



+ Training;



+ Update Training materials as required.



+ Conduct training to new colleagues as required.



+ Product Quality Review;



+ Perform proactive monitoring of test result trends.



+ Data trending for APRR.



+ Data trending of raw materials for reduced testing opportunities.



+ Laboratory investigation;



+ Conduct and document laboratory investigations in a timely manner according to SOPs.



+ Change Control Implementation;



+ Raise and complete change controls for changes with GMP impact.







Coordinate change controls to completion in a timely manner.







Education:







Degree or Diploma in Science (preferably Chemistry) or Chemical Process Technology.







**EXPERIENCE**







For a Diploma: A minimum of 5 years QC experience in the pharmaceutical or related industry.



For a Degree: A minimum of 3 years QC experience in the pharmaceutical industry.







Flexi Work - Tuas (Singapore)



Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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