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QC Specialist I
4 weeks ago
This role will be responsible for establishing and ensuring the testing of drug substance release and stability testing, including testing of intermediates in process control samples. Lab operations must be in accordance with written testing SOPs and local/international regulations.
About the RoleKey Responsibilities:
- Sample storage and management.
- Analytical testing and documentation of API / drug substance / drug product / finished product / complaints / stability / packaging material samples.
- Ensure all activities comply with cGxP, including data integrity.
- Stability testing (when not centralized):
- Testing and sample storage and management.
- Analytical documentation of stability samples to cGxP standards.
- Detect and report potential accidents and risks, and propose solutions.
- Preferred: Previous experience working in a pharmaceutical laboratory environment (quality assurance, production), aseptic techniques.
- Perform administrative activities in GMP and HSE-compliant, efficient production and documentation of standardized tasks.
- Engage in breakthrough analysis, demonstrate resilience, operational excellence, continuous learning, and be digital & tech savvy.
- Operate laboratory equipment, perform quality control testing and sampling, and possess knowledge of TQM and GxP standards and processes.
- Maintain laboratory excellence and support quality decision-making.
- Willingness to work in shifts.
- University degree or equivalent in Pharmacy, Chemistry, or related field, with 0-4 years of relevant experience.
Why Novartis: Helping people with disease and their families requires more than innovative science. It takes a community of passionate, smart individuals like you. Collaborate, support, and inspire each other to achieve breakthroughs that change patients' lives. Ready to create a brighter future together? Learn more
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SG12 (FCRS = SG012) Novartis Singapore Pharmaceutical Manufacturing Pte Ltd
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