Associate Scientist II, QC Raw Materials
PfizerAbout the role
Use Your Power for Purpose
Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard.
What You Will Achieve
In this role, you will:
Perform various chemical tests such as water analysis, FTIR, ID, HPLC, and other compendial assays.
Write and perform raw material verification protocols and associated reports.
Ensure training records are updated and correctly filed to reflect current testing capabilities.
Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions.
Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies.
Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current.
Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database.
Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on manager and working under their direction.
Working knowledge of compendial testing/requirements is preferred.
Here Is What You Need (Minimum Requirements)
Applicant must have a bachelor's degree with 0+ years of experience; OR an associate's degree with 4 years of experience; OR a high school diploma (or equivalent) and 6 years of relevant experience
Experience with analytical laboratory techniques/technologies
Experience with raw material enrollments
Knowledge of GMP guidelines
Knowledge and experience with Quality Systems
Strategic and Innovative Thinking
Expertise with analytical techniques such as: compendial testing, FTIR, GC, HPLC, etc.
Problem Solving and Critical Thinking Skills
Good Communication Skills
Bonus Points If You Have (Preferred Requirements)
Experience with using HPLC (High Pressure Liquid Chromatography) techniques
Proven track record in leading continuous improvement projects
Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis
Strong problem-solving skills and attention to detail
Ability to manage multiple priorities and meet deadlines.
Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels
Adaptability and willingness to learn new techniques and procedures
Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use
PHYSICAL/MENTAL REQUIREMENTS
Ability to lift, carry, push, or pull materials weighing up to 20 pounds.
Ability to work in a laboratory environment
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
This role is standard day Monday through Friday work shift
Other Job Details:
Last day to Apply: May 5th, 2026.
Work Location Assignment: On Premise
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