Duration : 02 / 09 / 2024 to 28 / 02 / 2025
For our Validation organization, we are currently looking for a Validation Specialist in our Small Molecules Business Unit. In this role, you will be responsible for pharmaceutical manufacturing process validation.
Key responsibilities :
Being part of the validation team for the process validation in the chemical plants
Ensuring the harmonization and compliant procedures for our Small Molecules Business Unit
Preparing process specific validation documents (protocols, reports, periodical reviews)
Assessing change requests and deviations
Participating in audits and inspections
Key requirements :
Bachelor's degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related field.
1-3 years of experience in pharmaceutical manufacturing process validation, preferably within a Small Molecules Business Unit.
Understanding of chemical processes and validation protocols.
Familiarity with GMP
Proficient in preparing and reviewing process-specific validation documents such as protocols, reports, and periodical reviews.
Ability to assess change requests and deviations effectively.
Business fluent in English; proficiency in German is a plus.
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