Site QA Manager at Global Leading Pharma (Kanto)

Take lead in QA activities for the company's site to ensure effective compliance. Manage manufacturing products are up to date aligning with QMS.
Client Details
* One of the leading global pharmaceutical companies in the industry
* Specializing in Immunology, Neurology, and rare disease for unmet medical needs
* Rich development pipeline focusing on new drug development and cutting edge innovative practices
* International organization with extensive global communication with stakeholders
Description
* Lead in QA activities for the business to ensure effective product quality for manufactured products
* Develop and maintain effective QMS at the site to ensure proper compliance with local regulations
* Make key decisions in batch release
* Educate and support cross functioning members in proper quality practice
* Improve continuous improvement activities and implement up to date GMP requirements, regulations, and systems
Profile
* University degree in scientific or related field
* High fluency in English and Japanese (non-native level speakers will not be selected)
* QA experience in pharmaceutical manufacturing environment with knowledge of drug production
* Strong understanding of GMP and other GxPs
* Ability to create GMP documents to align company SOPs
Job Offer
* Competitive salaries and benefits
* Great work life balance
* International working environment
* Work with industry leaders who are solving unmet medical needs
* Amazing career progression in QA
Page Group Japan is acting as an Employment Agency in relation to this vacancy.