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It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It
Manage own time, professional development and be accountable for own results.
Interpret and evaluate data in terms of accuracy, precision, trends, and potential Good Manufacturing Practices {also cGMP} impact and recommends appropriate corrective action where necessary.
Work effectively in a fast-paced, customer-oriented, team laboratory environment to analyze raw materials and packaging samples in support of the company's quality program in the chemistry laboratory.
Complete training activities and maintains records, equipment, basic lab supplies, and re-agents in accordance with {Current} Good Manufacturing Practices {part of GxP} requirements.
Participate in laboratory investigations as required.
Prepare Quality Performance Review.
Adhere to safe work practices, such as wearing appropriate personal protective equipment including lab coat, safety glasses, and gloves.
Perform equipment verification and calibration in accordance to procedures.
Maintain area and equipment in clean, safe, functional order.
Qualifications
Must-Have
High School Diploma or GED
2+ years' experience
Basic math and computer skills, such as data entry, along with a high level of attention to detail
Understanding of equipment, instrumentation, and computer applications
High productivity and the ability to multi-task coupled with a low error rate
Ability to read, comprehend, and follow procedures
Good oral, written and interpersonal communication skills within a diverse team setting
Nice-to-Have
Bachelor's Degree
Experience in a GMP environment
Quality Control experience in a pharmaceutical industry
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