QC Specialist I
1 day ago
Join to apply for the QC Specialist I - Analytical role at Novartis Singapore . This role is responsible for establishing and ensuring testing of drug substance release and stability testing, including testing of intermediates in process control samples. Laboratory operations must comply with written testing SOPs and local/international regulations. About The Role Key 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 and sample management when not centralized, with documentation to cGxP standards. Detect and report potential accidents and risks, proposing solutions. Essential Requirements Experience working in a pharmaceutical laboratory environment, including quality assurance, production, and aseptic techniques. Administrative skills and GMP/HSE compliance for efficient documentation and task execution. Skills in Breakthrough Analysis, Resilience, Operational Excellence, Continuous Learning, and Digital & Tech Savvy. Knowledge of laboratory equipment, QC testing, sampling, TQM, GxP standards, and laboratory excellence. Willingness to work in shifts. Desirable Requirements Degree in Pharmacy, Chemistry, or related field, with 0-4 years of experience. Why Novartis: Join a community of passionate people working to help those with disease, fostering collaboration, support, and innovation. Learn more: Novartis Strategy & Culture Join our Talent Network to stay connected and find suitable opportunities: Talent Network Benefits and Rewards: Learn more in our Benefits & Rewards Handbook. Additional Details Seniority Level: Entry level Employment Type: Full-time Job Function: Quality Assurance Industry: Pharmaceutical Manufacturing #J-18808-Ljbffr
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Qc Specialist I
5 days ago
Singapore Novartis Full time390536BR **QC Specialist I - Raw Materials**: Singapore **About the role** About the role: Key responsibilities - Maintain QC Raw Materials laboratory in full cGMP compliance. - Lead raw material method validation/ verification and routine release testing - Plan day to day operational activities in QCRM (i.e., housekeeping, release testing). Perform data...
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Qc Specialist
5 days ago
Singapore MiRXES Pte Ltd. Full time**QC Specialist** MiRXES is a Singapore-headquartered molecular diagnostic company with R&D, manufacturing, and clinical lab operations in Singapore, USA, Japan, and China. We specialize in microRNA technologies and the development, manufacturing, and provision of diagnostic test kits and clinical services. Our mission is to enable early disease detection...
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Qc Specialist
4 days ago
Singapore Kemin Full timeOverview: Kemin Industries (Asia) Pte. Ltd, Singapore, with manufacturing and research facilities in Singapore, is the regional headquarters for Asia Pacific, which includes Australia, China, New Zealand, Japan, Korea, Philippines, Thailand, Malaysia, Myanmar, Indonesia, Taiwan and Vietnam. We have vacancy for: **Position**:QC Chemist/QC...
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QA/qc Engineer
6 days ago
Singapore APPLIED ENGINEERING PTE LTD Full timeDuties and Responsibilities: a. Assist QA/QC Manager in the managing the QA/QC department b. Establish, implement and maintain the QC system for products that need to comply with ASME codes c. Prepare, control and maintain the QC Manual in accordance with ASME code d. Initiate quality programs and report to QA/QC Manager for the current product quality...
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qc inspector with cmm
2 weeks ago
Singapore I-LINK MANPOWER CONSULTANCY PTE. LTD. Full time $40,000 - $60,000 per yearQC inspector with CMMConduct daily incoming, in-process, and final inspections as assigned by the Qc Manager.Operate and program CMM (Zeiss) for dimensional inspections.Prepare and maintain QC inspection reports and related documentation,Perform measurements using micrometers, vernier calipers, height gauges, and profileprojectors.ldentify and report any...
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QA/qc Inspector
4 days ago
Singapore I Plus Q Human Resources Pte Ltd Full time**QA/QC Inspector ( Doing Material Inspection Role )** - Perform physical inspection of materials to ensure compliance with contract requirements. - Review the mill certificate for the materials for compliance to material standards /specifications. - Coordinate with client and 3rd party for inspection and approving materials for project use. - Establish and...
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QC Specialist
6 days ago
Singapore Pall Full time $60,000 - $120,000 per yearBring more to life.Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?At Pall Corporation, one of Danaher's 15+ operating companies, our work saves lives—and we're all united by a shared commitment to innovate for tangible impact.You'll thrive in a culture of belonging where you and...
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Qc Specialist
2 weeks ago
Singapore ANTER CONSULTING PTE. LTD. Full timeAbout the Role We are supporting a global pharmaceutical client in the setup and optimisation of their QC digital systems at a newly established API manufacturing facility in Singapore. This position focuses on supporting Empower Chromatography Data System (CDS) operations and related qualification and compliance activities within a GMP laboratory...
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Qc Associate
5 days ago
Singapore 10X GENOMICS PTE. LTD. Full time10x Genomics is looking for a QC Associate I to join its Quality Control team. This person will be responsible for the qualification of consumable products associated with Next Generation Sequencing chemistries. **What you will be doing** - Perform QC of consumables and instrumentation to defined procedures. Testing includes instrument QC, and consumables...
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Equipment specialist I
5 days ago
Singapore Novartis Singapore Full timeJoin to apply for the Equipment specialist I role at Novartis Singapore Join to apply for the Equipment specialist I role at Novartis Singapore Summary As Equipment Specialist, you will be responsible to produce pharmaceutical products by executing assigned activities according to production schedule in compliance with the relevant GMP, work, operating,...