Senior Compliance Specialist | Compliance Senior Specialist m/w/d 34,46€ plus Prämien

apero GmbH Arbeitnehmerüberlassung

Biberach an der Riß, Baden-Württemberg, Deutschland
Published May 10, 2026
Full-time
Permanent

Job Summary

The Senior Compliance Specialist will play a pivotal role in maintaining high quality standards within a GMP-regulated environment in Biberach. Your day-to-day responsibilities will involve managing complex GMP documentation, including CAPA, deviations, risk analyses, and effectiveness checks, ensuring all processes remain compliant with internal and regulatory requirements. You will actively support audits and inspections by preparing and presenting critical documentation. Furthermore, you will coordinate cross-functional compliance topics, acting as a key interface between internal and external stakeholders. This role is ideal for a detail-oriented professional with a strong background in life sciences who thrives in a structured, high-compliance setting. The position offers a stable, long-term opportunity with a reputable client, competitive compensation including bonuses, and opportunities for ongoing professional development within a supportive, employee-focused environment.

Required Skills

Education

University degree (PhD, Diploma, Master, or Bachelor) in Biochemistry, Biopharmacy, Biology, Chemistry, or Pharmacy; alternatively, a scientific master craftsman qualification (e.g., Pharmaceutical Master) with extensive experience in a GMP environment.

Experience

  • Several years of professional experience in biotechnological production, quality assurance, quality control, or a GMP/compliance environment.
  • Demonstrated experience in managing complex documentation and regulatory processes within a scientific or pharmaceutical setting.
  • Proven track record of coordinating interdisciplinary topics and managing internal/external stakeholder communications.

Languages

German (Fluent)English (Fluent)

Additional

  • Must be eligible to work in Germany. Willingness to participate in regular training and professional development as required by GMP standards.