vacancy for our Basel based client in the Pharma sector

Your tasks:

• Plan and execute tasks related to the creation of laboratory aliquots in the area of stability, release, and reference sample management at the site level
• Conduct/organise GMP aliquotting (laboratory „bulk“ and analytical samples in the mg/g range)
• Manage inventory (electronically and physically) on behalf of the analytical laboratory in centralised facilities
• Ensure delivery according to the relevant quality standards and compliance with systems, equipment, and processes
• Create raw data documents for handover to internal and/or external customers

Your experience/knowledge:

• Completed vocational training in pharmaceutical development/logistics in the GMP area or equivalent
• Minimum of 3 years successful professional experience in analytical development
• Good knowledge of software and computer tools
• Mastery of quality principles (GMP, ALCOA+)
• Language skills: German – fluent, English – good level

Ref.Nr.:

• Take the next step and send us your resume along with a daytime phone number where we can reach you
• Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens, and current work-permit holders for Switzerland
• We welcome applications from individuals of all genders, age groups, sexual orientations, personal expressions, ethnic backgrounds, and religious beliefs. Therefore, there is no requirement to provide gender information or a photo in your application
• As per client requirements, we need information about your marital status, nationality, date of birth, and a valid Swiss work permit. For applicants with disabilities, we are happy to explore potential solutions with our end client