Manufacturing and Supply
Where the
miracles of
science are made
a reality for patients

Job Overview

We are looking for Quality Assurance Specialist to join our Quality Assurance department in Lüleburgaz, Turkey.

Key Responsibilities

• Supporting the preparation and development of ISO9001, ISO27001, ISO14001 and OHSAS 18001 quality, environment, occupational health and safety management systems and performing the applications.

• Investigation and following deviation throughout the company and following their realization and reporting them periodically

• Playing role in teams related with improving the quality and decreasing the deviations in the department and throughout the company and contributing the implementation of the decisions taken during these team meetings. Following the implementation and actions of the deviations and change control systems on the site and reporting them.

• Evaluation of customer complaints, contributing them by investigating and reporting and giving feedback to the customers and reporting them

• Performing product quality review, reporting and evaluating them and determining the corrective and action plan with relevant departments if necessary.

• Reviewing the technical agreements to be signed internationally and with local customers and informing department manager

• Attending GMP/ISO9001 Quality Management System self-inspections, reporting and following the CAPA reports.

• Preparation before the customer and authority audits to be performed at facility, attending these audits and preparing the corrective and preventive action report related to own department after the audit and performing the actions on due time.

• Contributing the risk analysis studies during production, analysis and other process

• Preparing the standard operation procedures related with the works in the department

• Contributing the studies in order to comply with the department budget and targets.

• Providing technical support to company personnel for the studies he/she perform

• Supporting the development teams in the department and throughout the company and apply the decisions taken by this team in the department.

Requirements & Qualifications

• University education in Chemistry, Chemical Engineering, Biology or Pharmacy Faculty.

• Minimum 2 years of experience in QA department.

• Knowledge with GMP and GLP requirements

• Able to use MS Office, LIMS, SAP effectively

• Upper-Intermediate level in English

• Commit to customers, team oriented, result-focused, good communication skills

What Sanofi Can Offer You

• Benefits to enhance your life journey

• Development opportunities to own your future

• An open and inclusive environment where you can be yourself

• Social activities and wellbeing programs to support your life

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Pursue Progress. Discover Extraordinary.

Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.

Watch 'One day at Sanofi' and check out our Diversity Equity and Inclusion initiatives at sanofi.com