The role is responsible for ensuring product quality compliance with current GMP regulations through the verification of standard operating procedures and the use of appropriate tools
Job Summary
The role is responsible for ensuring product quality compliance with current GMP regulations through the verification of standard operating procedures and the use of appropriate tools.
Responsibilities include preparing international and local registration documentation, collecting and processing required information and certifications, and compiling regulatory-pertinent master data.
The company fosters an inclusive work environment where each person is considered an individual, respecting diversity and dignity, and recognizing employee merit.
Matching Summary
The role is responsible for ensuring product quality compliance with current GMP regulations through the verification of standard operating procedures and the use of appropriate tools.
Skills & Requirements
Must-have
Technical Regulatory Associate
Quality Systems
GMP compliance
International registration documentation
Local registration documentation
SAP master data compilation
Nice-to-have
Patient-inspired scientific progress
Inclusive work environment
Respect for diversity and dignity
Profoundly impact health for humanity
Key Requirements
Master's degree in Chemistry and Pharmaceutical Technology, Pharmacy, Chemistry, or Biology
12 months experience in pharmaceutical or similar sector