Senior Compliance Specialist | Compliance Senior Specialist (m/w/d)

Job Summary

As a Senior Compliance Specialist in the pharmaceutical industry, you will play a pivotal role in maintaining GMP compliance within Quality Control. Your day-to-day responsibilities include managing complex documentation such as CAPA, deviations, and risk analyses, while ensuring all processes meet national and international regulatory standards. You will act as a key interface between various departments, coordinating cross-functional compliance topics and preparing documentation for audits and inspections. This position is ideal for a detail-oriented professional with a background in life sciences who thrives in a highly regulated environment. You will work within a global pharmaceutical company, benefiting from a structured onboarding process and opportunities for professional development. The role requires strong organizational skills, the ability to communicate effectively across hierarchies, and a proactive approach to problem-solving. This is a unique opportunity to contribute to high-level quality standards in a dynamic, innovative, and collaborative team setting.