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

Job Summary

As a Compliance Senior Specialist, you will play a pivotal role in ensuring that our pharmaceutical projects meet the highest quality and safety standards. Your day-to-day responsibilities include managing GMP-related documentation, such as CAPA, deviations, and risk analyses, while ensuring full adherence to national and international regulatory requirements. You will act as a key interface between various departments, quality assurance teams, and external partners, coordinating complex compliance topics and preparing essential documentation for audits and inspections. Additionally, you will be responsible for conducting training sessions on compliance standards to keep the team updated on regulatory changes. This position is ideal for a detail-oriented professional with a background in life sciences who thrives in a collaborative environment and is eager to contribute to innovative projects within the pharmaceutical industry. You will benefit from a structured, high-performance environment that prioritizes professional development and long-term career growth.