Engineer ii, r&d
6 days ago
Provides technical documentation expertise in design control, NPR, CDP and related activities.
Job Description
Lead the design control activities for new product development and lead the change development process for current products.
Update the existing design control and related documents based on the changes.
Perform technical documentation review of designed products to ensure compliance with Cardinal Health design control procedures and regulatory requirements.
Prepare technical summaries of test reports and protocols.
Search and sort test data, test reports, and protocols for documentation compilation.
Provide technical documentation to support tender, customer questionnaires, and related activities.
Update technical specifications for materials, parts, and products.
Support External and Internal Audit for R&D Design Control & Design Transfer as required.
Review & conduct gap analysis on new revisions of standards.
Support new product registration projects as needed.
Qualification & Requirements
Possess a relevant degree in Engineering (i.e., Biomedical).
Minimum of four years of relevant experience preferred.
Prior working experience in product development of Medical Devices preferred.
Good understanding of Design Control for the Product Development process, CDP, standard requirements, and related activities.
Proficient in test report preparation, statistical analysis, and written and verbal communication.
Good working attitude, initiative-driven, and able to work independently.
This role requires working on-site at the R&D Lab based in Kallang and the ability to collaborate with Regional stakeholders.#J-18808-Ljbffr
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