Job Description

Why Patients Need You Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated and agile members, who understand the importance and impact of their role in Pfizer's mission. Patients need colleagues like you who take pride in their work and always look to improve outcomes.

ROLE RESPONSIBILITIES The role will review production Standards procedures, and take in charge investigations and deviations linked to processes and operation within the due dates. The role will Participate in Data Integrity program, strengthening the site data controls and individual accountability for the integrity of GMP (Good Manufacturing Practices) data at the site through facilitating education, awareness, improvement and reporting. Ensure that GMP (Good Manufacturing Practices) standards, as they apply to the individual products and the site, are in compliance with Pfizer and regulatory standards through implementing auditing and walkthroughs procedures and Ensure that appropriate systems are in place to meet or exceed the requirements of the company and the regulatory authorities for the quality of the products manufactured on site. Participate actively in realization of the site Site internal audit (SIA) by participating in internal audits/ walkthroughs, ensuring the follow-up on corrective/preventive actions, and will report findings in a clear, precise and factual way. Participate actively to ensure that the site is in a steady, ready, and prepared state for Inspection Readiness. The role will be Responsible for management of service provider supplier qualifications The role is responsible for an environment where standardization, continuous improvement and innovation in the production area are embedded in day-to-day operations through the IMEx framework and where plans for managing talent are developed. follow up of Continuous improvement projects establish connection between all Improvement elements and collect data to analyse loss root cause and support team to find good projects and Actions

BASIC QUALIFICATIONS AND PREFERRED QUALIFICATIONS Knowledge of investigation management, Data integrity principles and supplier management Bachelor, master in quality assurance or equivalent Strong Lean Manufacturing knowledge . Ability to quickly assess and assimilate technical data and conduct thorough investigations. Good written and verbal communication skills. Production and/or Quality Assurance experience. Understanding of Lean tools. Thorough understanding of current GMP (Good Manufacturing Practices) and regulatory aspects

ENVIRONMENT REQUIREMENTS Work Location Assignment: El Jadida

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

Manufacturing

#LI-PFE

4878710