Quasar Medical Singapore Pte Ltd – Associate Engineer – Quality Engineering

Company
Quasar Medical Singapore Pte Ltd
quasar-med.com
Designation
Associate Engineer - Quality Engineering
Date Listed
05 Dec 2022
Job Type
Entry Level / Junior Executive
Intern/TS
Job Period
From 04 Jan 2022, For At Least 6 Months
Profession
Engineering
Industry
Manufacturing General / Biomedical / Pharmaceutical
Location Name
Admiralty Street, Singapore
Address
Admiralty St, Singapore
Map
Allowance / Remuneration
$1,000 monthly
Company Profile

For over 30 years, Quasar has specialized in comprehensive turnkey solutions, offering our clients a wide range of manufacturing capabilities, professional support, and project optimization—from the initial process design to mass production. This integrative approach to process development provides our clients superior quality and cost-efficiency. Quasar holds all internationally relevant certificates (ISO 13485:2016; cGMP compliance) and emphasizes very strict controls in IP protection.

Quasar has a global presence, with headquarters in Singapore, and Hong Kong, engineering offices in Israel, two manufacturing facilities in China, a new manufacturing facility in Thailand, and a business development unit in the United States. With more than 2,900 employees, Quasar is a market leader in the area of manufacturing minimally invasive medical devices. Our clientele includes large, multinational companies like Johnson & Johnson, Medtronic, and Abbott.

With more than 1.5 Million sensors produced per year, Quasar is a leading manufacturer of micro-sensors used in minimally invasive devices. Weare experts in electromagnetic, thermo, proximity, location, pressure sensors. 

Quasar has mastered under-microscope assembly running the most advanced production lines, combining both human and automated processes. Allow us to manufacture complex minimal invasive medical devices such as balloon catheters, guide wires, micro-electronic components, micro-pacemakers, electrode catheters, and much more. 

Job Description

Support Quality Engineers on their day to day product quality activities that includes:

  • Maintain and comply with the requirements of IS013485, GMP, FDA 21 CFR Part 820 and other applicable regulations.
  • Establishing inspection standards, plans, frequencies and test methods.
  • Support and drive cost improvement project
  • Drives robust and effective corrective and preventive action programs through the CAPA system.
  • Support Production on all quality-related activities, including working closely with Engineering and other applicable functions.
  • Assist in the investigation and analysis of customer complaints and follow-up with the relevant functions to ensure that they are addressed & closed in a timely manner.
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