Job title : GMP Audits Manager - Third Parties // Gerente de Auditorías de Calidad - BPM Location: Bogotá, Colombia About the job Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions and consumer healthcare. As a company with a global vision of drug development and a highly regarded corporate culture, Sanofi is recognized as one of the best pharmaceutical companies in the world and is pioneering the application of Artificial Intelligence (AI) with strong commitment to develop advanced data standards to increase reusability & interoperability and thus accelerate impact on global health. The Global M&S Services acts as a cornerstone to this effort. Our team is responsible for delivering and supporting Global M&S teams in partnership with Business and Digital, and drive priority and transformative initiatives across M&S. Main responsibilities: Provide QA and Technical Support to Third Party Manufacturers (TPM) and Contract Manufacturer Organization (CMO), TPM/CMO Operations, Affiliates, and other Stakeholders. Responsible for compliance with Corporate and Divisional QA policies, procedures, standards, and specifications as well as country specific regulations depending on the TPM location and markets. Ensure compliance to Corporate and Divisional QA requirements and identify and/or resolve Quality gaps and/or issues relating to product design, manufacturing quality programs and product start-ups at TPMs. Responsible for overall quality and safety of products manufactured at those facilities. Utilize understanding of QA systems and problem-solving tools to provide alternative solutions to quality issues. Manage supplier audits, ensuring cGMP and SOP alignment. Track market developments, regulatory changes. Follow up on CAPAs. Participate in audits, inspections, interface with specialists. Provide an assessment of supplier's quality in place with regards to material compliance, as well as regulatory of CAPA before communicating it to be the request sites. Being a local quality contact between the Suppliers, Global Quality Suppliers & IA sites to facilitate follow up of improvements and exchange of quality information. Support audits lead by other auditors when specific expertise is needed (e.g. for cause audit with user sites representatives, highly sophisticated topic) Conduct on-site and remote audits of GxP and Health Regulated Third Party vendors to ensure compliance with regulations and company policies. About you Experience: 4+ years of experience in Third Audit Parties. 7-10 years of related experience in the pharmaceutical industry. Thorough knowledge of cGMPs, Code of Federal Regulations in drugs and biologics. Should be knowledgeable in Quality functions of pharmaceutical industry. Experience in conducting on-site audits, inspections and facing regulatory/health authority inspections/audits. Thorough knowledge of CAPA systems is required and experience is desirable. Thorough knowledge of and experience in application of GMP requirements. Experience managing third party manufacturers and/or contract manufacturer organization is preferred. Experience of working on manufacturing sites is an added advantage. Required skills: Excellent problem solving and decision-making skills are critical to this position. The successful candidate must be able to demonstrate their risk-based decision-making ability. Proficient in problem-solving, attention to detail, and good organizational skills. Work in a team-oriented, flexible, and proactive manner. Analytical skills and ability to multitask in a stressful environment. Education: Master's or Ph.D. in Life Sciences/Healthcare, or related technical field. Languages: Excellent knowledge of English language (spoken and written). 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. Pursue Progress . Discover Extraordinary . At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity. 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