Join a leading global pharmaceutical company and become a key player in ensuring quality assurance within analytical activities that contribute to the development of innovative medicines. This role is situated in a dynamic environment where quality, collaboration and scientific excellence are paramount.

As a suitable candidate, you are a motivated Quality Assurance Specialist with a strong background in quality assurance and analytical development. If you are passionate about maintaining high quality standards and thrive in a diverse team, this position might be the right fit for you.

• You serve as the QA point of contact for internal and external analytical laboratories within Analytical Development.
• You oversee GMP compliance of analytical activities, including method development, validation, transfer and stability studies.
• You review and approve analytical documentation, such as validation protocols, reports and method transfer documents.
• You assist in managing deviations, CAPAs, change controls and audits.
• You ensure methods and processes are developed, validated, and transferred according to global regulations and quality requirements.
• You collaborate with global QA and Analytical Development teams to harmonize quality standards.
• You contribute to a culture of quality, collaboration and continuous improvement.