CELL ID PTE LTD 源鉴定

• Electro-chemistry (R&D) Specialise in:​

  • Biosensor

  • 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)

  • 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.

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•  Software Engineer (R&D)​ 

(Requirement: BSc, MSc, Ph.D with min. 3 years in related fields,         Singaporeans only)​

​

• • ​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.

  • 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.

  • 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.

  • ​

• Quality Section Manager​

• • (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.

  • Improve company products' quality towards a cost-saving lean manufacturing concept.

  • To perform to the highest quality and conform to customers' feedback, complaints, requirements and expectations.

  • Support R&D in their evaluation and development of new products by means of prototypes and pilot runs.

  • Initiate the process of product & process evaluation validation according to regulatory guidelines.

  • Establish and maintain the quality management system according to ISO 13485 and ISO 17025; and to comply with HSA legislation and regulations

  • Establish and maintain the documentation system required to support the quality management system

  • 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

  • Follow up and verify the implementation of solutions, corrective and preventive actions

  • Perform supplier audits and qualification; establish and maintain Approved Vendor List

  • Formulate, implement and ensure smooth operation of quality plans and procedures

  • any other assigned Quality related activities