Senior Expert - QC job opportunity at Novartis.

Home Jobs In Singapore Tag: Job Senior Expert - QC position at Novartis


DateMore Than 30 Days Ago bot
Novartis Senior Expert - QC
Experience: 6-years
Pattern: full-time
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degreeAssociate
loacation Tuas South Avenue, Singapore
loacation Tuas South Ave..........Singapore

Job Description Summary Primary responsibilities for this position include performing tasks associated with release testing and reviewing laboratory data, coordinating the team/lab under its responsibility. Communicating with internal & external partners for the Quality Control organization. Supports site as technical expert in related field   Job Description Key Responsibilities: Act as SME in the area of equipment calibration and qualification in the QC laboratory ensuring compliance with local and global procedures while minimising the impact on the business Coach trainers to ensure effective training of QA/QC analysts in area of laboratory equipment and qualification by developing and advising standardized content, materials and assessment tools. Act as SPOC for major QC equipment projects and liaise closely with end users and other departments in relation to cross-functional projects Management of QC investment budget/QC asset management and utilisation/QC CapEx projects. Troubleshoot and resolve challenging issues relating to modifications of current quality compliance processes and systems within and across various functions to ensure all health, safety or training procedures meet requirements. Lead cross functional project teams to drive team results including Lab Excellence projects Initiate and supervise the Strive to constantly continuous improvement of systems and practices on site with respect to achieve compliance, reducing waste and improving efficiencies Stand in for other team members in the QC Support Services team in their absence. Essential Requirement: BS: 6+ years related experience with 3+ years in management Related experience should be in GMP-regulated industries in Quality Control. Must have a working knowledge of health authority and regulatory requirements as well as industry quality management tools, standards, and quality systems. Must have an understanding of pharmaceutical industry trends and practices. Broad cGMP experience is required with knowledge and understanding of manufacturing, quality control, and validation requirements and activities. Desirable Requirement: English fluent in speaking and writing. Mandarin Chinese a plus   Skills Desired Continued Learning, Dealing With Ambiguity, Decision Making Skills, Gxp, Industry Standards, Laboratory Equipment, Laboratory Excellence, Managing Resources, Organizational Savvy, Quality Control (Qc) Testing, Quality Control Sampling, Self-Awareness, Smart Risk Taking, Technological Expertise, Total Quality Management

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