Hybrid Manager, Stability

Posted 2 hours ago

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About the role

  • 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

Benefits

  • Flexibility for U Program: 2 day remote working

Job title

Manager, Stability

Job type

Experience level

Mid levelSenior

Salary

Not specified

Degree requirement

Bachelor's Degree

Location requirements

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