Gracias por tu interés en unirte a Solventum. Solventum es una empresa nueva en el ámbito de salud, pero con una sólida experiencia en la resolución de desafíos que transforman vidas y fortalecen el trabajo de los profesionales de la salud. En Solventum, las personas son el centro de cada innovación que desarrollamos. Con empatía, conocimiento y criterio clínico, trabajamos en conjunto con los líderes más destacados del sector para enfrentar los retos más complejos de nuestros clientes. Mientras continuamos actualizando nuestra Página de Carreras y los materiales dirigidos a los postulantes, es posible que algunos documentos aún muestren la marca anterior. Ten en cuenta que todas las oportunidades laborales publicadas pertenecen a Solventum, y que la Política de Privacidad mencionada https://www.Solventum.Com/en-us/home/legal/website-privacy-statement/applicant-privacy/a cualquier información personal que proporciones. Al igual que en 3M, en Solventum se brinda igualdad de oportunidades a todos los candidatos calificados, sin distinción de raza, color, religión, sexo, orientación sexual, identidad de género, origen nacional, discapacidad o estatus como veterano protegido. En Solventum, desarrollamos soluciones innovadoras para enfrentar los retos más complejos de nuestros clientes, liderando avances en salud mediante la combinación de ciencia médica, de materiales y de datos. Nuestro propósito es mejorar la vida de los pacientes y apoyar a los profesionales de la salud para que se desempeñen de la mejor manera posible.Job Description:Area Quality Specialist3M H ealth C are is now S olventumAt Solventum, we enable better, smarter, safer healthcare to improve lives.



As a new company with a long legacy of creating breakthrough solutions for our customers' toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue.We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you.The Impact You'll Make in this RoleAs an Area Quality Specialist, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by:Manage and govern the company's document control system (ENOVIA), ensuring review step compliance with local requirements.Monitor, analyze, and drive performance against key quality KPIs, ensuring timely disposition and continuous improvement.Lead cross-functional investigations and manage the development, implementation, and effectiveness monitoring of Corrective and Preventive Actions (CAPAs).Conduct annual site risk assessments, develop, execute, and oversee internal audit and self-inspection programs.



Supports external audits per Technical Director instructions and integral procedures.Deliver training and qualification programs to employees on QMS requirements and quality processes.Partner with the Technical Director to ensure ongoing compliance with applicable regulatory, quality, and operational requirements.Support product release activities, including oversight of Certificates of Analysis (CoAs) and related quality documentation.Manage change control processes, including documentation, impact assessment, implementation, and effectiveness tracking.Act as the designated backup for the Technical Director, ensuring uninterrupted oversight of quality and regulatory compliance activities when required.Undertake additional responsibilities as assigned by management to support organizational priorities and continuous improvement initiatives.Your Skills and ExpertiseBachelor's degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, Healthcare, or a related field (completed and verified prior to start date).Minimum of three (3) years of experience maintaining Quality Management Systems (QMS) and Good Distribution Practices (GDP) within Medical Devices and/or Pharmaceutical environments.Intermediate to advanced English proficiency, with the ability to communicate effectively in a global environment.Strong knowledge of Medical Device and Pharmaceutical regulations, including Good Storage, Distribution, and Transportation Practices.Experience conducting internal audits, risk assessments, CAPA management, change controls, and regulatory inspections.Additional qualifications that could help you succeed even further in this role includeStatistics and data analysis for quality performance monitoring and continuous improvement.Experience in Regulator#J-18808-Ljbffr

📌 Area Quality Specialist (Cundinamarca)
🏢 Solventum (3M Healthcare)
📍 Cundinamarca