CorDx Jobs in Singapore

+ Manage and coordinate IVD and biomedical research projects + Perform project data input for internal systems and collaborations with third parties + Plan project timelines, milestones, and deliverables Bachelor's / Master's / PhD in Biomedical Science, Biotechnology, Life Scie ...

Regulatory Affairs Executive responsible for product registration including preparation of registration dossier design of performance evaluation study and manage execution and communication with CRO. · Product registration: · Be the subject matter expert on medical devices laws a ...

Carry out basic quality checks on incoming in-process and finished IVD products and materials. · Check product labeling packaging and documents according to approved procedures. · Record inspection results and keep quality and inventory records up to date. · ...

Assist in the preparation of reagents and quality control products according to established SOPs. · ...

Manage and coordinate IVD and biomedical research projects. · ...

Manage and coordinate IVD and biomedical research projects · Perform and maintain project data input for internal systems and collaborations with third parties · ...

Assist in the preparation of reagents and calibration materials according to established SOPs. · ...

Assist in the preparation of reagents and quality control products according to established SOPs. · ...

Assist in the preparation of reagents, calibration materials, · and quality control products according to established SOPs · Maintain accurate records of raw and supplementary materials usage, · ensuring proper labeling and traceability. · ...

Assist in production tasks such as preparing reagents materials monitoring inventory quality control products. · ...

Manage · Perform and maintain project data · Plan and manage project timelines · Allocate and track budgets, · Monitor project progress, · Coordinate with internal teams, · Prepare project updates, ...

This is a quality management system executive role in Singapore. · ...

Develop and maintain Quality Management Systems in compliance with ISO regulations for medical devices. · ...

Manage coordinate IVD biomedical research projects plan project timelines milestones deliverables allocate track budgets costs resources monitor project progress risks issues coordinate internal external teams prepare project updates reports documentation. · ...

Develop and implement strategies for vouchers pricing product expiry and page design across e-commerce platforms such as Shopee Lazada Amazon Shopify CorDx online store etc Design product listings including images and descriptions to enhance visibility and sales Create manage cus ...

Regulatory affairs executive responsible for product registration and compliance in regions of interest. · ...

Assist in the preparation of reagents and calibration materials according to established SOPs and support inventory management by monitoring material usage and reporting low stock levels. · ...

Carry out basic quality checks on incoming IVD products and materials. Record inspection results and keep quality records up to date. · ...

+Develop and implement strategies for vouchers, pricing, product expiry and page design across e-commerce platforms such as Shopee Lazada Amazon Shopify CorDx online store etc · ++Design product listings including images and descriptions to enhance visibility sales Create custome ...

The Regulatory Affairs Executive will be responsible for product registration including preparation of registration dossier and managing execution and communication with CRO. They will also be the subject matter expert on medical devices laws and regulations for product registrat ...