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QC Specialist II

2 weeks ago

Singapore Novartis Farmacéutica Full time

This role utilizes chemistry laboratory skills to test and measure product or raw materials while ensuring that analysis is performed according to established Standard Operating Procedures (SOPs), Analytical Methods & current Compendia.
About the Role
Key Responsibilities:
Sample storage and management - Analytical testing/documentation of incoming raw material samples to GxP standards.
Reporting of technical complaints/adverse events/special case scenarios related to Novartis products within 24 hours of receipt.
Distribution of marketing samples (where applicable).
QC testing of all incoming raw materials as per cGMP standards.
Familiarity with major pharmacopeia standards such as USP, EP, JP/JPE, ChP etc.
Deadline adherence rate: testing completed on time, all missed deadlines reported in good time.
Ensure constant readiness for inspection, no critical complaints/observations from superiors and inspectors.
Consistently follow the GMP and GDP guidelines, as well as the SOPs, with no critical irregularities.
Finding and implementing optimization options to reduce costs.
Completed training plan.
Sound technical & scientific knowledge of pharmaceutical/chemical.
Working experience in Laboratory environment in the Pharmaceutical analytics/QC/equivalent industry.
Why Novartis:
Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us
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