Key skills
RSAPProject Management
About this role
Role Overview
- 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
Benefits
- Flexibility for U Program: 2 day remote working