GMP Specialist (m/f/d)

Ihre Aufgaben:

• Lead and manage CAPAs and actions from deviations, ensuring timely and effective implementation.
• Conduct thorough investigations of deviations to determine root causes and develop appropriate CAPAs.
• Document all CAPA activities in compliance with GMP regulations and company procedures.
• Maintain inspection readiness by continuously improving compliance processes and documentation.
• Work closely with QC-CLs to ensure alignment on CAPA implementation and compliance improvements.

Ihr Profil:

• MSc in Pharmaceutics, Analytical Chemistry, or a related field. A PhD is an advantage.
• Minimum of 2 years of experience working in a GMP environment with a strong focus on HPLC and GC analytics.
• Demonstrated expertise in analytical method validation, and troubleshooting.
• Strong knowledge of GMP regulations and guidelines.
• High attention to detail and a commitment to maintaining the highest standards of quality and compliance.