Sr Quality Specialist
Aplica ya
Mapa de ubicación: Marburg, Hesse, Germany
Full time
R1414141
Descripción del trabajo
Duties and Responsibilities:
- Provide coordination and oversight and ensure GCLP compliance regarding equipment qualification, calibration and maintenance, Change management as well as Deviation & CAPA management
- Validation Owner for computerized systems and IT-applications
- Ensure timely completion of processes and workflows
- Manage equipment SOPs lifecycle as well as qualification and validation documents
- Supports the implementation of new quality requirements
- Drive spot checks, audit/inspection preparation and audit/inspection follow up
- Manage spot checks for the lab areas in coordination with QA
- Support preparation of audits / inspections (documentation and logistics)
- Support CAPA plan development and ensure timely follow up in response to audit & inspection observations
- Participation in regular meetings locally and globally in order to ensure harmonization of procedures and processes
Requirements:
- Bachelor's degree in biology, biochemistry, life science or a similar degree program.
- At least three years of professional experience in the relevant field, ideally in the qualification, calibration and maintenance of GCLP compliance equipment
- Experience of working in a GxP environment
- Very good written and spoken German and English language skills
- Good computer skills (especially MS-Office package).
Q² Solutions,IQVIA’s laboratory business, creates connected intelligence by combining our expertise, technology and analytics - this fuels unparalleled research & development solutions. We uphold a deep commitment to patients, sites, customers, and each other. https://www.q2labsolutions.com/careers
Únase a la red de talentos de IQVIA
Regístrese hoy y le informaremos cuando haya puestos disponibles que coincidan con sus intereses profesionales.
Únase a nuestra red