Job Description

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 make sure that product and process documents match the specifications based on established 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 be involved in working through, change control activities, product complaint investigations, and developing and maintaining processes per Pfizer Standards to ensure compliance with configuration management policies. As an associate, your focus on the job will contribute in achieving project tasks and goals as asssigned. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues. It is your hard work and commitment that will make Pfizer ready to achieve new milestones and help patients across the globe. How You Will Achieve It Contribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team. Review Manufacturing and Packaging records to ensure that the information and documentation conforms to Pfizer policy and cGMP\'s. Create, review changes, investigations and consistently produce quality work. Accurately communicate supply, operational needs or Quality Operations (QO) perspectives and escalate issues with potential market or stability impact. As required assist with the review of documents received in the batch release area for completeness and accuracy. To assist with trainings. To maintain documentation related to SOPs, GMP records. Maintain inspection readiness, support inspections from regulatory agencies & customers and improve quality assurance systems. Participate in Projects related to Quality initiatives. as appropriate. Assist and support the team in detecting and solving compliance errors. Help to define appropriate action plans for improvement and follow-up and communicate action closures. To maintain Quality data into Pfizer digital systems for Quality. To create Change controls and review in the Pfizer Change management system. To create presentations related to Quality as appropriate. Qualifications Must-Have Master\'s degree in science, M Pharm (Microbiology/ Biotechnology/ Chemistry, Quality Assurance) Sound knowledge of current Good Manufacturing Practices part of GxP Ability to work in a team environment own team and interdepartmental teams. Effective written and oral communication skills Good hands-on Microsoft Office tools, Microsoft Presentations, Excel, word, etc. Nice-to-Have Experience at a manufacturing site basic knowledge of Quality Management Systems 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

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