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← Simtra BioPharma Solutions

Associate Director Quality Compliance / QA Client

Simtra BioPharma Solutions
Location
Halle, North Rhine-Westphalia, Germany
Posted
20 days ago
Department
Quality Assurance & Regulatory Affairs
What they actually want (must-haves)
  • PhD or Master's degree in Pharmacy, Biology, or a comparable natural science field
  • More than 10 years of professional experience in the pharmaceutical GMP environment, ideally in sterile manufacturing or CDMO
  • Solid experience in Quality Assurance and comprehensive knowledge of FDA and EMA requirements
  • Several years of leadership experience, preferably at least 5 years in managing QA teams
  • Experience in establishing and managing inspection readiness programs and leading regulatory inspections
  • Strong communication and leadership skills
What the job really is

As the Associate Director of Quality Compliance at Simtra, you will lead the Quality Compliance and QA Client areas, ensuring adherence to regulatory requirements and the development of the quality management system. Your responsibilities include managing teams focused on client communication, auditing, data integrity, and release management, as well as overseeing audit readiness and representing the quality department during inspections and audits.

Benefits
  • Modern in-house cafeteria with attractive subsidies
  • 30 days of vacation plus special leave
  • Job bike leasing
  • Corporate benefits: exclusive discounts for employees at numerous well-known brands
  • Good transport connections and free employee parking
  • Financial support for job-related relocations as part of our relocation cost package
Things to weigh
  • No salary listed
  • The role requires extensive experience in a highly regulated environment, which may limit the candidate pool
  • Focus on compliance and quality management may not appeal to those seeking more diverse responsibilities
Job score3.4/5
Benefits4/5
Freshness4/5
Career value4/5
Role clarity5/5
Pay transparency0/5

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