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. You will play a crucial role in improving patients' lives by ensuring the highest standards of quality and safety in our products. Your leadership will be instrumental in driving innovation and excellence, ultimately making a global impact on patient health.

What You Will Achieve

In this role, you will:

Lead people, technology, and financial resources in QC finished products and Microbiology sections.Identify and develop innovative concepts for process or product improvements, taking calculated risks to achieve results.Solve complex problems, leveraging experience from various areas as needed.Recognize and address development needs, creating growth opportunities for colleagues.Lead , oversee and/or manage multiple projects and ongoing work activities, ensuring compliance with approved methodologies and cGMP documentation.Provide technical expertise and support for laboratory and core applications, collaborating with business partners to identify and implement improvement areas.Utilize IMEx methodology and tool “Lean &sigma” to lead continuous improvement activities in QC laboratoryConduct , oversee and/or review/approve investigations, CAPA (Corrective Action and Preventive Action) and change controls.Review laboratory data to ensure compliance with approved methodologies.
Build capabilities of the Process-Centric Team according to skills needs assessments.Provide technical expertise and support to the QC laboratory for laboratory and core applications.Manage review and approval of Good Manufacturing Practices ‘’ cGMP’’ documentation, such as procedures, analysis data and reports.Manage work streams Quality Control Finished Good, Stability, cleaning/process validation, Microbiology and Methodology sections.Responsible for developing Quality control Finished Good, Stability and Methodology sections colleagues and prepare Succession plan for the Finished Good, Stability and Methodology sections.Responsible for QC analyst qualification programAct as site SME for Stability and microbiology.

Here Is What You Need (Minimum Requirements)

Bachelor’s degree in a relevant scientific discipline with 5+ years’ experienceLaboratory supervisory experience in FP, Stability and/ or MicrobiologyProven experience in leading colleagues and managing projectsA deep understanding of Good Manufacturing Practices (cGMP) compliance requirements for Quality Control LaboratoriesProficiency with Quality Control instruments and methodologies Microbiology and/ or Finished products analyticalExperience in lean manufacturing and sigma concepts and toolsKnowledge of cGMP /Saudi FDA compliance requirements for Quality Control LaboratoriesProficiency in Laboratory Information Management Systems like Empower and SAP quality moduleSolid understanding of method qualification and testing of components and finished productsSolid understanding of Data integrity requirementsExperience in microbiological risk assessmentsStrong problem-solving skills and the ability to think outside the box.

Bonus Points If You Have (Preferred Requirements)

Master’s degree or higher in a relevant scientific disciplineLean six sigma certifications.2+ years of experience in leading people  
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