Monitor and evaluate suppliers based on defined commodity strategies, identifying opportunities to consolidate suppliers and reduce the overall supplier base where appropriate.
Conduct technical analysis and assessment of new FA/outsourced parts, and support Category Buyers in supplier selection and technical evaluation.
Manage and maintain new supplier Request for Quotation (RFQ) activities, including technical clarification, quotation evaluation and cost comparison.
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Bachelor’s degree in a relevant field such as Biomedical Engineering, Health Sciences, Pharmacy, or related discipline.
Attention to detail, strong organizational skills, and the ability to manage multiple projects and deadlines.
Effective written and verbal communication skills, with the ability to present regulatory information clearly to internal and external stakeholders.
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Proficiency with the Spring Framework and related tools within the Java ecosystem.
Familiarity with RESTful APIs, databases (SQL/NoSQL), and version control systems such as Git.
Understanding of software development best practices, including code reviews, unit testing, and continuous integration/continuous delivery (CI/CD).
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High attention to detail, time management, and planning abilities to manage multiple tender deadlines and ensure compliance with all submission requirements.
Comfort with productivity and collaboration tools (e.g., word processing, spreadsheets, presentation software, and email/CRM systems).
Diploma or degree in engineering, business, management, or a related field is preferred; relevant experience in tendering, bids, or proposals will be an advantage.
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Shall qualify or prepare working standards as per the requirement.
Online documentation of raw data, entries of logbooks and system calibrations in time, ensure compliance to SOPs, GLP and Good documentation practices.
Maintain the management of chemicals, HPLC and GC Column, reference standard and working standard as per the SOP.
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To assist in analytical development and responsible in testing of samples for the related BI projects.
Execute formulation trials for product quality improvement and alternative / new materials evaluation, reviewing of trial results and update project progress status in a timely manner.
Responsible for technical document preparations required by RA, QA and other relevant departments; to ensure record traceability for the improvement projects’ experiment / test data.
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