Job Description

###

Summary

Execution of assigned tasks in the quality control laboratory in accordance with cGxP regulations. Performance of laboratory specific activities such as analyses, maintenance, calibration and qualification of analytical equipment.
###

About the Role

Key Responsibilities:

Operational

Sample storage and management Analytical testing and documentation of API / drug substance / drug product / finished product / Complaints / stability / packaging material samples Ensure all activities in compliance with cGxP, incl. data integrity Stability (when not centralized) + Testing/Sample storage and management
+ Analytical documentation of stability samples to cGxP standards

HSE

Comply with all HSE guidelines Detect and report potential accident, risks and propose solutions Responsible for participating in initial training and retraining

Essential Requirement:

Preferred: Previous experience working in a laboratory environment in the pharmaceutical industry (quality assurance, production), aseptic technique. Collaboration; result-oriented Administrative activities and GMP and HSE-compliant, efficient production and documentation of standardized tasks in the infrastructure Breakthrough Analysis; Being Resilient; Operational Excellence; Continuous Learning; Digital & Tech Savvy Laboratory equipment; Quality Control (QC) Testing; Quality Control Sampling; knowledge of TQM and related industry GxP standards and processes; Laboratory Excellence; Quality decision making Must be willing to work in 12hrs rotational shift.

Desirable Requirement:

Completed apprenticeship as a laboratory assistant or equivalent training Basic (oral and written) in English; fluent in local language (oral and written)

Why Novartis:

Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients' lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Join our Novartis Network:

Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network

Benefits and Rewards:

Read our handbook to learn about all the ways we'll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards



Division
Operations
Business Unit
Quality
Location
Singapore
Site
Tuas South Avenue
Company / Legal Entity
SG12 (FCRS = SG012) Novartis Singapore Pharmaceutical Manufacturing Pte Ltd
Functional Area
Quality
Job Type
Full time
Employment Type
Regular
Shift Work
No

Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.