Scientist I, Project QA
Core
Ensuring quality compliance and regulatory adherence in pharmaceutical technology transfer, batch production, and validation processes.
Role type
Scientist I, Project QA
Builds
Compliant pharmaceutical products and validated manufacturing processes
Domain
Pharmaceutical manufacturing / Quality Assurance
Required skills
GMP regulations knowledge, batch record review, validation protocol review, deviation management, change control, product release, audit preparation, analytical method review, investigation report writing
Preferred skills
Organic Chemistry or Pharmaceutical Engineering background, bilingual communication (Chinese/English), problem analysis
Technologies
GMP, VMP, validation protocols
Responsibilities
Review technical documents for technology transfer, execute batch record reviews, review quality standards and analytical methods, lead change control and deviation management, host customer audits, review deviation and investigation reports
Seniority
Entry-level (Fresh graduates welcome)
