Haw Par Healthcare Limited – Quality Assurance Intern

Company
Haw Par Healthcare Limited
hawpar.com
Designation
Quality Assurance Intern
Date Listed
13 Dec 2025
Job Type
Entry Level / Junior Executive
Free/ProjIntern/TS
Job Period
From 03 Mar 2026 - Flexible End
Profession
Sciences / Laboratory / R&D
Industry
Manufacturing General / Biomedical / Pharmaceutical
Location Name
2 Chia Ping Road, Singapore
Address
2 Chia Ping Rd, Singapore 619968
Map
Allowance / Remuneration
$800 - 2,600 monthly
Company Profile

About Haw Par Healthcare Limited

Haw Par Healthcare Limited is a Singapore-based healthcare company known for its trusted wellness brands, including Tiger Balm, distributed in over 100 countries. We are committed to high standards of quality and Good Manufacturing Practices (GMP), providing valuable exposure to regulated QA and QC processes for interns and contract staff.

Job Description

About the Role

We are looking for a QA Temp/Intern to support our Quality Assurance and Quality Control teams. This role is suitable for students or fresh graduates seeking short-term exposure to QA processes within a healthcare manufacturing environment. Contract duration: 3 months (From March 2026) 

Responsibilities

  • Assist in maintaining and updating QA and QC documents (hardcopy and electronic).

  • Support the preparation, revision, and filing of technical and GMP-related documents.

  • Perform data entry and assist in compiling QC test results for record-keeping.

  • Assist in issuing, tracking, and organising logbooks and controlled forms.

  • Help maintain training records and training materials.

  • Provide administrative support such as photocopying, scanning, and preparing documents for audits or internal reviews.

Requirements

  • Diploma/Degree students or graduates in Life Sciences, Chemistry, Biomedical Science, Pharmaceutical Science, or related fields.

  • Comfortable with documentation, data entry, and administrative tasks.

  • Good attention to detail and ability to follow procedures.

  • Able to commit full-time for 3 months.

What You Will Gain

  • Exposure to GMP documentation practices in a healthcare/OTC manufacturing environment.

  • Hands-on experience with QA and QC processes.

  • Understanding of controlled documents, logbooks, and regulatory compliance workflows.

  • Opportunity to support audits and real QA operations.

 

Application Instructions

Discuss this Job:

You can discuss this job on Clublance.com #career-jobs channel, or chat with other community members for free:
Share This Page