Quality Control & Inventory Intern

Company

Kinexcs Pte Ltd

kinexcs.com

Designation

Quality Control & Inventory Intern

Date Listed

22 Jul 2026

Job Type

Entry Level / Junior Executive

Intern/TS

Job Period

Immediate Start, For At Least 6 Months

Profession

Industry

Location Name

20 Ayer Rajah Crescent, Singapore

Address

20 Ayer Rajah Cres., Singapore 139964

Map

Allowance / Remuneration

$800 - 1,200 monthly

Company Profile

Quality Control & Inventory Intern

Company Overview:

Kinexcs is an AI-driven digital health platform and wearables company with a mission to enable and empower people for mobility and a better quality of life. It is focused on reducing the burden of musculoskeletal conditions, which affects about 25% of the world’s population. The flagship product, KIMIA Recover, a continuous monitoring device for the knee joint, has obtained FDA Approval, CE marking and HSA approval. KIMIA Recover is a comprehensive recovery management solution providing reduction in number of hospital visits and complications for knee patients.

Kinexcs' digital platform uses artificial intelligence for MSK assessment and therapy. This platform is capable of providing pre-consultation assessments and real-time exercise guidance and feedback to musculoskeletal patients, and is being adopted by some of the largest private healthcare providers and corporates.

Job Description

ROLE SUMMARY

Build practical experience at the intersection of quality, engineering and operations in a regulated medical device environment. The intern will take ownership of defined assignments, work with cross-functional teams and apply academic knowledge to real quality and operational challenges. The role combines structured learning with hands-on exposure, data review, documentation and process-improvement work, enabling the intern to develop transferable skills for a future career in engineering, quality, manufacturing or operations.

KEY RESPONSIBILITIES

• Conduct quality evaluations of components and finished devices using approved procedures and tools, while developing practical skills in quality assurance and accurate documentation.

• Maintain quality records, traceability information, and controlled documentation in accordance with company procedures, gaining practical exposure to ISO 13485 quality management principles.

• Collaborate with cross-functional teams and contribute to continuous-improvement activities through the review of existing workflows and the development of practical enhancements.

• Gain hands-on exposure to assembly and inventory activities to build an understanding of day-to-day medical device operations.

WHAT YOU WILL GAIN

• Practical familiarity with medical device quality-management principles aligned with ISO 13485, including good documentation practices, nonconforming material controls, traceability, and audit-ready recordkeeping.

• Hands-on experience in quality evaluation, controlled documentation, and inventory-related activities within a regulated medical device environment.

• Career-relevant skills in process review, problem-solving, professional communication, and the development of practical improvement recommendations.

REQUIREMENTS

• Pursuing or recently completed a diploma or degree in engineering, life sciences, quality, manufacturing, operations, supply chain or a related discipline.

• Curious, proactive and detail-oriented, with an interest in learning through both analytical and hands-on work.

• Basic spreadsheet, data-handling and documentation skills.

• Good written and verbal communication skills, with the ability to work effectively with others.

• Prior industry experience is not required.

General note: This job description outlines the primary responsibilities of the role and is not exhaustive. Related duties may be assigned based on operational needs and appropriate training.

Application Instructions

Please apply for this position by submitting your text CV using InternSG.
Kindly note that only shortlisted candidates will be notified.