QA Lead (GMP)

Your Responsibilities:
Purpose

To lead and manage quality compliance issues related to manufacturing and batch usage decision activities to maintain cGMP compliance in line with GSK and regulatory standards.

Key Responsibilities:

Job Responsibilities

•Lead and coach a team of QA Executives to perform the following which includes
◦ Interact with manufacturing personnel in day-to-day operations
◦Support compliance in production areas by routinely conducting QA checks
◦Authorize campaign changeovers and participate in facility walk downs where required
◦Provide QA input and assistance in managing unplanned event investigations, CAPA implementation and change control monitoring
•Provide QA consultation
•Escalation to Line and Head on key progresses and issues
•Propose site improvement strategies
•Other activities assigned (internal audits, KPI reporting etc)

Why You?

Basic qualifications:
•Degree in Science or Engineering
•Extensive knowledge and hands-on experiences of pharmaceutical manufacturing processes
•Efficient communication skills
•SAP experience preferred
•Ability to apply risk management skills effectively

Preferred qualifications:
•At least 6 years of experience in Pharmaceutical industry preferred

Why GSK?:
GSK Vaccines has a broad portfolio and innovative pipeline of vaccines to protect people of all ages. We deliver over two million vaccine doses per day to people living in 160 countries, preventing a range of diseases such as; hepatitis, rotavirus and HPV infections, diphtheria, tetanus, whooping cough, measles, mumps, rubella, bacterial meningitis and influenza. Our Tuas site, one of only two GSK global vaccines manufacturing facilities worldwide, operates around-the-clock to manufacture the active ingredient used to make a GSK vaccine that protects children against pneumonia.

Contact information:
You may apply for this position online by selecting the Apply now button.
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