Your responsibilities include reading, correcting, writing, and reviewing production-related documents
Job Summary
Your responsibilities include reading, correcting, writing, and reviewing production-related documents.
You will provide on-site support for product quality maintenance and development through oversights, gemba, internal audits, and validation activities.
GSK is an international pharmaceutical company with the mission to help people live active, feel better, and live longer lives.
Matching Summary
Your responsibilities include reading, correcting, writing, and reviewing production-related documents.
Skills & Requirements
Must-have
document review and correction
on-site quality support
GMP compliance
night shift work
Nice-to-have
resilience in complex situations
organizational skills
dialogue and tolerance
risk assessment
Key Requirements
Bachelor's degree in science or A2 diploma with 10+ years experience
Minimum 5 years biopharmaceutical production experience