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

• The incumbent will be responsible for QC sample approval/lot disposition in the Quality Control laboratory.
• Involved in capacity planning and work forecast to ensure optimal efficiency in resources utilization.
• Responsible for conducting Laboratory Investigation on Out of Specification / Questionable QC test results and deep dive for root cause determination and effective Corrective Action and Preventive Action (CAPA) implementation.
• Responsible for managing the training of Quality Control laboratory personnel.
• Involved in the management of stability program and associated activities in the Quality Control laboratory.
• Support data analysis and trending of QC data for annual product record review (APRR).
• Responsible to work with cross functions to ensure completion of activities.
• Understand GMP principles in the QC laboratory and comply with Data Integrity requirements (ALCOA+)
• Ensure the audit readiness and presenting during audits as SME.

Here Is What You Need (Minimum Requirements)

• Bachelor's degree/Associate's degree with 3 years or Diploma with 5 years of QC experience in the pharmaceutical industry or related industry
• Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations
• Knowledge of Good Manufacturing Practices and its application standards, processes, and policies.
• Excellent organizational skills and strong ability to multi-task
• Strong written and verbal communication skills

Bonus Points If You Have (Preferred Requirements)

• Experience with laboratory work
• 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

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