Manager for stability studies within Grifols, a global healthcare leader in plasma-derived medicines. Overseeing development projects and compliance with regulatory standards.
Responsibilities
Plan, coordinate, and oversee assigned development and stability study projects
Lead the planning and execution of development projects and stability studies
Define the technical strategy and ensure adherence to deadlines and objectives
Design and optimize products, materials, and manufacturing processes
Coordinate multidisciplinary teams and monitor project progress
Analyze and interpret experimental results to inform decision-making
Ensure compliance with applicable regulations (GMP, GLP, among others)
Oversee the preparation and review of technical and regulatory documentation
Prepare for and attend regulatory audits
Manage the department's budget and ensure the efficient use of resources
Requirements
Degree in in Pharmacy, Chemistry, Biotechnology, Chemical Engineering, or a related field
Master's degree in the Pharmaceutical and Parapharmaceutical Industry is a plus
Advanced level of English (C1)
Experience in stability studies and product development in regulated environments (GMP, GLP) (Indispensable)
3 – 5 years of experience in similar roles within R&D in the pharmaceutical or biotechnology industry
Experience in scientific project management
Previous experience in team management will be highly valued.
Proficient in the Office and have basic SAP user skills
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