GMP Documentation Specialist – Pharma

Siegfried AG in Irvine, CA seeks a documentation and quality/compliance professional to ensure GMP documentation and batch records are complete and accurate.

You will collaborate across manufacturing and QA, review investigations and deviations, write CAPA actions, and help ensure on-time product release and regulatory compliance.

Strong attention to detail, knowledge of cGMPs, and ability to work with multiple departments are essential in this role.

Join us at Siegfried AG as our next GMP Documentation Specialist – Pharma in Irvine, CA, United States.

This is an excellent opportunity to take on the GMP Documentation Specialist – Pharma role at Siegfried AG.

As a GMP Documentation Specialist – Pharma, you will play an important part at Siegfried AG in Irvine, CA, United States.

We invite applications for the GMP Documentation Specialist – Pharma position located in Irvine, CA, United States.