Quality Specialist Pharma | Quality Specialist Pharma (m/w/d)

Job Summary

As a Quality Specialist in the pharmaceutical sector, you will play a pivotal role in ensuring that all operations strictly adhere to Good Manufacturing Practice (GMP) standards. Your day-to-day responsibilities include maintaining and developing the quality management system, managing deviations, CAPA processes, change controls, and risk management. You will be responsible for drafting and reviewing critical GMP-relevant documentation such as SOPs and reports, while actively participating in the preparation and follow-up of audits and inspections. This position offers a unique opportunity to work on diverse, high-impact projects for renowned clients within a collaborative, interdisciplinary environment. You will be expected to bring a structured, quality-oriented mindset to the team, contributing to continuous process improvements. The role is ideal for a professional with a background in life sciences who is eager to drive sustainable developments and advance their career within a supportive, forward-thinking organization that values both professional and personal growth.