The role involves leading and coordinating projects for source changes, process improvements, and technical transfers within a global healthcare innovation environment
Job Summary
The role involves leading and coordinating projects for source changes, process improvements, and technical transfers within a global healthcare innovation environment.
Candidates must independently drive process, packaging, and cleaning validations while ensuring full compliance with cGMP and other regulatory requirements.
The position requires utilizing Six Sigma techniques to investigate site non-conformances and determine root causes through scientific problem-solving.
Matching Summary
The role involves leading and coordinating projects for source changes, process improvements, and technical transfers within a global healthcare innovation environment.
Skills & Requirements
Must-have
5+ years pharmaceutical experience
Solid and non-solid dosage forms expertise
cGMP compliance knowledge
Six Sigma and Lean methodology
Technical transfer and validation execution
Root cause analysis using scientific methods
Nice-to-have
Cross-cultural communication skills
Innovation and change management mindset
International audit experience
Strong project prioritization abilities
Agility in handling stretched deadlines
Key Requirements
Bachelor's or Master's degree in Pharmaceutical Science, Engineering, or Science
Minimum 5 years of experience in a pharmaceutical environment
Proficiency in English for cross-cultural technical communication
Knowledge of Chinese NMPA regulations and GMP requirements