Activités Industrielles
Là où les miracles
de la science
deviennent une réalité pour les 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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Toujours Progresser. Découvrir l’Extraordinaire.

Rejoignez Sanofi et entrez dans une nouvelle ère de la science – où votre parcours peut être aussi transformateur que le travail que nous accomplissons. Nous investissons en vous pour que vous alliez plus loin, accélériez votre réflexion et accomplissiez ce qui n’a jamais été fait auparavant. Vous contribuerez à repousser les limites, à bousculer les conventions et à concevoir des solutions plus intelligentes pour les communautés que nous servons. Prêt·e à poursuivre les miracles de la science et à améliorer la vie des gens ? Poursuivons le progrès et découvrons l’extraordinaire – ensemble.

Chez Sanofi, nous croyons dans l’égalité des chances, sans distinction de race, de couleur, d’ascendance, de religion, de sexe, d’origine, d’orientation sexuelle, d’âge, de citoyenneté, d’état civil, de handicap, d’identité de genre ou de tout autre critère protégé par la loi.