Engineer, Supplier Quality III
- A jornada completa
- Workday Global Grade: 15
Descripción de la empresa
La misión de AbbVie es descubrir y ofrecer medicamentos y soluciones innovadores que resuelvan los problemas serios de salud abordando los desafíos médicos del mañana. Nos esforzamos por tener un impacto notable en la vida de las personas en varias áreas terapéuticas claves (inmunología, oncología, neurociencia y cuidado de los ojos) y en los productos, servicios de nuestra cartera en Allergan Aesthetics. Para obtener más información sobre AbbVie, visítenos en www.abbvie.com. Siga a @abbvie en Twitter, Facebook, Instagram, YouTube y LinkedIn.
Descripción del empleo
Support and follow up the suppliers to ensure that quality relevant materials and services meet specifications and Company requirements.
Keep approved suppliers in compliance and document the entire process to meet the requirements of regulatory agencies and QMR03 Supplier Controls policy.
Coordinate with other areas of the Company to comply with the procedures and goals established in the area.
MAJOR RESPONSIBILITIES
• Open, notify, track progress and close SCARs (supply corrective actions) to suppliers. Approve closure of SCARS as Quality Contact in GTW system.
• Track blocked, on hold and quarantine materials to determine a material disposition to comply with the business goals or metrics. Review and approve material disposition of non-conforming materials.
• Attend CoE of supplier metrics and supplier controls. Escalate to management any relevant issues, corporate procedures changes and projects managed by CoE.
• Support and execute activities related to assigned projects, such as assurance of supply, new product introduction, transfer products or process, sustaining and qualification of suppliers, supply change notifications, etc.
• Receive change notifications from local and international suppliers and share them with the Global GSQM department. Lead and evaluate the change by forming an interdisciplinary team that provides support in the impact evaluation that may be generated in each of the company's departments.
• Preparation, coordination and execution of First Articles and Change Plans related to the evaluation of materials affected by change notifications or new qualifications.
• Review that material specifications for new material qualification or material changes are adequate for the incoming of the material.
• All other duties inherent to the position and those assigned by his/her immediate supervisor, including opening and actions related to deviations, NC’s, CAPAS, DCC’s, CCs, AIAs, CFT meetings, TRs, FSFA and internal audit responses.
Requisitos
- Bachelor's degree in electrical, mechanical, electronic, electromechanical, industrial engineering, biotechnology, chemistry.
- English B2+ (C1 prefered)
- 3 year of experience in regulated industries with expertise in supplier quality management.
- Experience as Supplier/Internal Auditor is a plus.
- Experience or certificates on electrical, mechanical, electronic, electromechanical field is a plus.
- High knowledge in root cause determination tools, such as DMAIC or A3, among others and CAPA system.
- Quality Management Systems/regulations (GMPs, QSR, FDA, ISO, CAPA).
- Advanced knowledge of Office applications (Windows)
- Ability to communicate written and oral ideas in a clear, concise and precise manner.
- Visa & Passport (Nice to have)
Información adicional
AbbVie es un empleador que ofrece igualdad de oportunidades y se compromete a operar con integridad, impulsar la innovación, transformar vidas y servir a nuestra comunidad. Empleador que ofrece igualdad de oportunidades, veteranos y discapacitados.