Quality Control Analyst

Use Your Power for Purpose

Everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is flexible, innovative, and customer-oriented. You will play a crucial role in improving patients' lives by ensuring the highest standards of Good Manufacturing Practices (GMP) are met. Your work will directly contribute to the safety and efficacy of our products, making a tangible difference in the lives of patients worldwide.

What You Will Achieve

In this role, you will:

• Perform analytical testing accurately and efficiently following Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) requirements.

• Perform Analytical Method Transfer, Analytical Method Validation and Analytical Method verification as well as Cleaning Method Development and Validation in accordance with Standard Operating Procedures (SOPs), adhering to ALCOA principles and Data Integrity requirements.

• Interpret and evaluate data in terms of accuracy, precision and potential Good manufacturing Practices impact and recommend appropriate corrective actions.

• Support to QC Method trouble shooting.

• Support the troubleshooting and resolution of equipment and testing issues, ensuring operational readiness.

• Manage and maintain reagents and laboratory consumables inventories, ensuring they are valid and stored correctly.

• Support routine data review following written procedures.

• Review and revise Standard Operating Procedures (SOPs), analytical methods and related procedures/documents, to keep them current.

• Maintain training to current standards and procedures on all assigned curriculums

• Participate in Laboratory investigations and propose CAPA for the identified root cause.

• Contribute to the completion of improvement projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.

• Manage personal time and professional development, being accountable for results.

• Maintain data integrity and ensure compliance with company SOPs, GLP and cGMP regulations.

• Use IMEX "way of working" for day-to-day operations, problem solving, escalation and continuous improvements.

• Participate in 5S team initiatives and practice good housekeeping, ensuring all safety procedures for site and QC laboratories are followed.

Here Is What You Need (Minimum Requirements):

• Bachelor's degree (Chemistry, Biology, Biotechnology or similar)

• At least five years of working experience with HPLC techniques in analytical laboratory (knowledge of working in Empower environment is a plus)

• Demonstrated technical skills in method transfer, method validation and cleaning validation.

• Knowledge of laboratory equipment, testing, and techniques

• Knowledge of Good Manufacturing Practices and its application standards, processes, and policies.

• Excellent organizational skills and strong ability to multi-task across various projects and activities

• Strong written and verbal communication skills (French and English)

• High level of attention to detail

• Self-motivated and able to work in minimal direction

• Broad experience with Microsoft Office products

Bonus Points If You Have (Preferred Requirements):

• Proven track record in leading continuous improvement projects

• Strong problem-solving skills and attention to detail

• Ability to manage multiple priorities and meet deadlines.

• Ability to work independently and as part of a team

• Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels

• Adaptability and willingness to learn new techniques and procedures

• Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity.

 
Work Location Assignment: On Site

Worker Type: Regular

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