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
In your role, you have the all-important task of preparation and review of required documentation, such as Good Manufacturing Practices, Good Laboratory Practices (GLP), Good Clinical Practices (GCP) manuals. You will be relied on to prepare procedure manuals, quality control manuals, engineering documents, manufacturing instructions, and change authorizations in accordance with company policy and government regulations. Your organizing skills will help you implement related documentation systems, propose change control processes and coordinate the review of procedures and forms. You will also provide input on quality control procedures and R&D documentation.
As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues.
It is your focus and dedication 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.
• Execute the tasks to support the Quality Systems functions.
• Work within the Quality system including usage of Pfizer Document Management System (DMS) to ensure quality and compliance.
• Oversee Documentation Control and other key administration functions of the DMS repository including the establishment of new processes leveraging the new repository to meet regulatory requirements.
• Coordinate with cross functional teams for documents issuance, retrieval and storage of Good Manufacturing Practices {also cGMP} documents.

Qualifications
Must-Have

• Master's Degree with 2 years/ Bachelor's degree with 5 years
• Demonstrated experience in Document Management and Control
• Familiar with Computer Software Validation Concepts
• Ability to gain insight into the diverse processes in sterile injectables manufacturing and apply this knowledge in the creation of simplified instructions 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
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