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
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
#LI-PFE
Demo
Singapore, Singapore
Full Time