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The Company

Our client is one of the top multinational biotechnology companies who strives to serve patients by transforming the promise of science and biotechnology into therapies that have the power to restore health or save lives.

 

Role Description

Your role as a GMP Asoociate QA is to provide guidance and support to production staff in compliance with the Standard Operating Procedures and work instructions.

 

Responsibilities

- Responsible in performance batch record review of batches assembled and labeled.

- Responsible in reviewing and approving batch production data entries before production activities.

- Responsible in performing GMP compliance checks in production.

 

Requirements

-Has MBO or Bachelor’s degree in Life Sciences or any related field.

-Has at least 3 years of experience in Quality Assurance or manufacturing experience in the pharmaceutical industry

-Has expert experience in GMP, GDP, or GCP.

 

Other Information

If you think this role is for you and you want to explore more of the possibilities, please contact Leri Salve Lapore and apply via the button below.