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• Simon Moser

Personal information

• Wants

  Ensuring that activities are performed to high standards of quality and timeliness in line with the best industry standards. Advances in analytical technology & pharmaceutical development.

• Haves

  Coordinate and supervise daily operations of the raw material and finished product teams, ensuring on-time completion for multifaceted projects. Improve GMP by eliminating non-conforming processes and results. Approve product testing and release documents. Engineering IQ/OQ/PQ. FDA cGMP Guidance for Industry Process Validation. ______________________________________________________________________________________ Performe QC release testing and sampling in high throughput environment, ensuring that raw materials and finished products aligne with company and regulatory standards.

• Interests

  Maintain open communication with QA, QC, regulatory and production departments for seamless execution of all initiatives.

• Organizations

  Quality Control & Assurance (QC/QA)

• Groups

  

• Employment status

  Employee

Educational background

• Languages

  English (Fluent), German (First language), French (Fluent)