Your new challenges which will inspire you: 

• Prepare validation documents and other GMP-relevant documents with the support of senior analytical specialists and team leaders
• Develop and validate methods
• Support troubleshooting in the QC laboratories
• Manage sample administration and follow-up of validation-related testing in the QC and R&D laboratories
• Support method transfer and the issue/update of product specifications
• Administer documents required for submission and assist with inspection tasks
• Prepare statistical evaluations of data and reports using Excel

Your profile that will convince us:

• University degree (MSc, PhD, or equivalent) in Chemistry or Biosciences
• Work experience in the pharmaceutical industry, especially in the field of method validation (GMP environment), is a plus
• Willingness to travel for business (approx. 5% per year, domestically and internationally)
• Good knowledge of MS Word and MS Excel
• English communication skills (oral and written)
• Strong social and presentation skills
• Strong problem-solving, organizational, and time-management skills. Ability to multitask and a high level of flexibility