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Job Title: Third Party Management Specialist

Main Responsibilities:

• Evaluating and qualifying new Third Party and when applicable, certifying Third Party based on their quality systems, capabilities, performance history and Quality Control expertise.

• Ensuring that all third-party activities comply with relevant legal and regulatory requirements (e.g., QSMP).

• Ensuring proper documentation and record-keeping of all third-party quality activities and communications.

• Driving continuous improvement initiatives with Third Parties to enhance product quality and process efficiency.

• Developing and maintaining quality agreements and Technical Specifications (PTS, STS) with Third Parties, outlining quality expectations and responsibilities.

• Establishing an annual audit program of third-party facilities to assess compliance with applicable regulatory requirements (GMP / GDP) and internal documents.

• Identifying and mitigating risks associated with Third Parties through risk assessments and implementation of corrective actions.

• Ensuring the resolution of quality issues related to Third Parties, including audit observation, deviations, non-conformances, and Third Party complaints as well as supporting customer complaints.

• Monitoring the progress and timely implementation of any CAPA addressing quality issues or supporting continuous improvement

About you:

• Bachelor's degree (Life Sciences, Business Administration or related fields - preferred)

• A combination of education and experience will be considered.  

• 1+ years of experience in third-party quality management systems, QA or related areas in the pharmaceutical industry.

• Experience using Veeva.

• Experience in quality management systems in the pharmaceutical industry.

• Ability to analyze complex data, identify trends, and make data-driven decisions to improve quality and compliance.

• Strong verbal and written communication skills to effectively interact with third-party suppliers, internal teams, and regulatory bodies.

• Proficiency in conducting thorough and effective audits of third-party suppliers to ensure compliance with quality standards and regulations.

• Excellent problem-solving abilities to address and resolve quality issues, including root cause analysis and implementation of corrective actions.

• Strong project management skills to oversee multiple quality initiatives, manage timelines, and ensure successful completion of projects

• Fluent in English, both written and spoken.

Why choose us?

• Bring the miracles of science to life alongside a supportive, future-focused team.​​ 

• Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.​​ 

• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.​​ 

• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.​ 

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law. 

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All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

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