Pharmaceutical Production Specialist / GMP Expert | Pharmakant/in

Job Summary

This role involves acting as a key expert in a GMP-regulated pharmaceutical or biotech production environment, focusing heavily on quality assurance and process improvement. Day-to-day responsibilities include drafting and reviewing quality-relevant documentation such as SOPs and manufacturing specifications for bulk production, managing deviation reports, conducting root cause analyses, and implementing corrective and preventive actions. The specialist will coordinate and provide technical support for various projects, manage change requests, and actively identify and implement improvements in routine production processes. Key requirements include proven professional experience in a GMP setting, strong knowledge of relevant regulations, and familiarity with improvement methodologies like Six Sigma or Lean. This is an attractive opportunity to apply expertise in a dynamic, full-time role within a globally operating corporation, requiring fluent English and proficient German communication skills.