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Johnson & Johnson is seeking a Senior Process Engineer to lead and coordinate projects related to the supply of APIs, materials, and process improvements in a pharmaceutical setting in Xi'an, China. The ideal candidate will have significant experience in pharmaceutical engineering, with a strong focus on compliance, project management, and technical communication skills.
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Job Summary
Leads and coordinates projects for source change of APIs, excipients, packaging materials, process improvements, technical transfer, and introduction of new technology under supervision.
Drives related validations independently and efficiently, including process, packaging, and cleaning validations, and completes investigations for site process non-conformances using scientific problem solving and six sigma techniques.
Ensures full compliance with cGMP, finance, and other regulations while effectively communicating with stakeholders and facilitating resolution of business partner issues.
Matching Summary
Match Score: 75
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Johnson & Johnson is seeking a Senior Process Engineer to lead and coordinate projects related to the supply of APIs, materials, and process improvements in a pharmaceutical setting in Xi'an, China. The ideal candidate will have significant experience in pharmaceutical engineering, with a strong focus on compliance, project management, and technical communication skills.
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Skills & Requirements
Must-have
Pharmaceutical manufacturing processes expertise
Process validation and technical transfer
Six Sigma and lean concepts
cGMP compliance
Statistical data analysis
Cross-cultural technical communication
Nice-to-have
Project management skills
Team leadership and coordination
Innovative and change-driven mindset
Customer and business focus
High sense of responsibility
Ability to work under pressure
Key Requirements
Minimum 5 years pharmaceutical experience
Bachelor’s or Master’s degree in Pharmaceutical Science, Engineering or Science
Knowledge of Chinese NMPA drug registration and GMP regulations
English proficiency for technical communication
Experience in pharmaceutical regulations and GMP requirements