As a QC Laboratory Analyst, you will contribute to team deliverables, perform tasks in compliance with quality standards, evaluate lab data, and participate in investigations while ensuring adherence to Good Manufacturing Practices. This role emphasizes effective teamwork and problem solving in a fast-paced lab environment.
Use Your Power for Purpose
Every day, Pfizer's unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients.
What You Will Achieve
In this role, you will:
- Take responsibility for individual contributions to achieve team deliverables, working effectively as a team member and coordinating with others.
- Manage personal time and professional development, being accountable for results.
- Follow standard procedures to complete tasks of varying scope, sequence, and complexity within the agreed timeframe.
- Identify and solve moderately routine problems.
- Complete assignments with moderate supervision using established procedures, referring deviations from standard procedures to the supervisor.
- Ensure work is reviewed for accuracy, quality, and adherence to standards.
- Evaluate and interpret data for accuracy, precision, and trends, considering the impact on Good Manufacturing Practices (cGMP) and recommending corrective actions when necessary.
- Operate efficiently in a fast-paced, customer-oriented team environment, analyzing raw materials and packaging samples to support the company's quality program in the chemistry lab.
- Complete training activities, maintain records, equipment, basic lab supplies, and reagents in compliance with Current Good Manufacturing Practices (part of GxP) requirements.
- Participate in laboratory investigations and Quality Performance Reviews.
Here Is What You Need (Minimum Requirements)
- High School Diploma or GED with 1+ years of relevant experience
- Basic math and computer skills such as data entry
- Understanding of equipment, instrumentation, and computer applications
- High productivity and the ability to multi-task
- Ability to read, comprehend, and follow procedures
- Good oral, written, and interpersonal communication skills within a diverse team setting
- Experience in a GMP environment
Bonus Points If You Have (Preferred Requirements)
- Quality Control experience
- Strong problem-solving and analytical skills
- Ability to work independently with moderate supervision
Work Location Assignment: On Premise
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
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