Why Patients Need You Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients.
Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented.
Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.
What You Will Achieve You will be a member of Pfizer's dedicated and highly effective quality assurance team.
You will evaluate and review Pfizer's clinical and commercial batches of drugs.
You will make sure that product and process documents match the specifications based on established sampling and statistical process control procedures.
Your expertise will help in identifying deviations from established standards, in the manufacturing and packaging of products.
In the relevant cases you will approve investigations and change control activities to ensure compliance with configuration management policies.
As a QA Specialist, your knowledge and skills will contribute towards the goals and objectives of the team.
Your focus and ability to meet team targets will help in completing critical deliverables.
Your innovative use of communication tools and techniques will facilitate in explaining difficult issues and establishing consensus between teams.
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 Job Responsibilities: Support operations through real time batch review ensuring all batch manufacturing records (paper / electronic) and associated manufacturing deviations are reviewed in a timely manner and in accordance with release schedules.
Support issue resolution, incident routing and deviations Complete walkthrough audits to ensure the area is maintaining cGMP compliance standards.
Attend IMEx meetings and ensure timely escalation of issues to the QA Manager Accurately communicate Supply/Operational needs/perspectives as well as Quality Operations (QO) perspectives.
Review and approval of validation documents Process, cleaning