Job description

In this diverse and responsible position, you will play a key role in providing analytical support for an international pharmaceutical project. Your core tasks will include:

• Support in the project and resource planning of all analytical activities at the site in close collaboration with the local project manager and the local team.
• Independent coordination, execution and documentation of method transfers, method developments, validations and verifications of sophisticated analytical procedures (e.g. HPLC, AAS, KF) – both internally and with external laboratory partners.
• Independent execution of analytical tests including protocol and report preparation in accordance with GMP and internal quality standards.
• Evaluation of existing methods with regard to practicality, regulatory requirements (EU/US GMP) and validation status; further development and revalidation if necessary.
• Independent solutions to methodological and device-specific questions – supported by the expert network of a global company.
• Identification of optimization potentials with regard to method modernization, robustness and efficiency.
• Assisting with the review and control of laboratory records, plans and reports from other ATS projects, as well as the preparation of specification documents.
• Preparation of analytical documents for official submissions.
• Supporting multiple analytical transfer activities in parallel.