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 AchieveYou will be recognized as a subject matter expert with specialized knowledge and skills in procedures, techniques, tools, materials and equipment. You will be entrusted with adapting standard methods and procedures by applying your knowledge, prior work experience and requirements. Your business awareness of cross-organizational impact on project delivery will elevate the quality of project deliverables. You will arrive at decisions on which methods and procedures are the best fit for different work situations.You will train others and reinforce behaviors that will help us achieve our goal of providing the best healthcare to our patients.How You Will Achieve ItManage own time, professional development and be accountable for own results.Prioritize own workflow, allocate work of others and assist in establishing their priorities, pushing self and others to exceed goals.Ensure compliant and timely documentation and resolution of events.Maintain a high level of personal safety and housekeeping considerations.Identify Continuous Improvement opportunities and participates in Continuous Improvement projects.Author /review QC (Quality Control) documentation and document all results in accordance to Good Manufacturing Practices and Good Laboratory Practices requirements.Responsible for the endorsement of Good Laboratory Practices {part of GxP} Environment, Health & Safety requirements and Pfizer Quality Standards (PQS) requirements.Ensure compliance with all policies and procedures in accordance with the Company Handbook.Provide training for team members and perform peer reviews of data and logbooks.Perform sampling and tetsing of raw materials in accordance with approved procedures and test methods, and record the test results in timely mannerPerform sampling and testing of water samples, following approved schedule and procedures, and record the test results in timely manner.Manage retained samples of raw material to ensure all retained sample available, stored in appropriate condition and record in accordance with approved procedureSupport procurement team related to raw material changes.Support regulatory team related to regulation submission process.Assist Lab Supervisor or QC Manager in laboratory investigation process.Maintain stock of reagents, column, and other supplies used in QC Chemical lab. Ensure all reagents and reference standards are valid and stored according to requirement. Ensure all equipment are calibrated and in a good condition before use.Develop or revise SOP or Form in Laboratory, if necessaryMaintain Lab Area and facilities in a clean, orderly and operational stateQualificationsMust-HaveHigh School Diploma or GED6+ years’ experienceCertification in assigned area, if applicableSampling and testing abilityAbility to write clear technical document.Good organizational and time management skillsGood oral and written communication skillsGood Microsoft Office skillsNice-to-HaveBachelor's DegreePharmaceutical and quality control experienceEffective problem solving skills 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