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Electro-chemistry (R&D) Specialise in:
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Biosensor
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Reagents, Assays, Probes.
(Requirement: BSc, MSc, Ph.D with min. 3 years in related fields, Singaporeans only)
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Maintenance Engineer (Shift-Work)
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Mechatronics / Electro-mechical
(Min. Diploma with experience preferred)
Interested applicants may submit your CV to info@cid.com.sg .
Only shortlisted candidates will be notify.
(Requirement: BSc, MSc, Ph.D with min. 3 years in related fields, Singaporeans only)
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Software engineering:
‐ Responsible for software development life‐cycle.
‐ Responsible for creating and maintaining System/Product Functional Requirements Specification to meet the customers and regulatory requirements.
‐ Responsible for System/Product Verification and Validation.
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In the area of firmware development:
‐ Collaborate with the Electrical Engineer to design, develop and validate the embedded firmware for the medical device.
‐ Firmware for new product design/development, product enhancements and/or product/material change requests.
‐ Responsible for the firmware release management.
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Key member of new product introduction (NPI) team
‐ Responsible for the software aspects of integration of methods, man and machines/tools to bring products into production.
‐ Participate in vendor discussions, acceptance tests and validation tests of mfg tools/machines and facilities needed for the
production of the customers' products.
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Quality Section Manager
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(Requirement: BSc., MSc, with min. 3~5 years of related field experiences. Singaporean only)
Primary responsible to lead the Quality Assurance Department to achieve Company's goals and objectives. Management Representative for all QMS related activities.
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Improve company products' quality towards a cost-saving lean manufacturing concept.
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To perform to the highest quality and conform to customers' feedback, complaints, requirements and expectations.
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Support R&D in their evaluation and development of new products by means of prototypes and pilot runs.
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Initiate the process of product & process evaluation validation according to regulatory guidelines.
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Establish and maintain the quality management system according to ISO 13485 and ISO 17025; and to comply with HSA legislation and regulations
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Establish and maintain the documentation system required to support the quality management system
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Liaise with customers and suppliers on all quality related matters.
Initiate actions to prevent the occurrence of non-conformities relating to product, processes and quality management system
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Follow up and verify the implementation of solutions, corrective and preventive actions
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Perform supplier audits and qualification; establish and maintain Approved Vendor List
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Formulate, implement and ensure smooth operation of quality plans and procedures
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any other assigned Quality related activities