QC Analyst (1 Year Fixed Term Contract) at Haleon

Haleon; Kuala Lumpur; On-site; MYR 48,000 - 72,000; Full time

Job summary

Haleon in Kuala Lumpur, Malaysia, is seeking a QC Analyst for a 1 Year Fixed Term Contract. This on-site, full-time role supports analytical testing, method validation, and GMP/GLP compliance within a dynamic quality control environment.

The ideal candidate has a chemistry-related degree, familiarity with HPLC and dissolution testing, and up to 3 years of QC/QA experience or fresh graduates with strong academics. Strong teamwork and meticulous record-keeping are essential.

Qualifications

• Bachelor's degree in Chemistry, Pharmaceutical Science or Analytical Science.
• Fresh graduates are encouraged to apply.
• 1–3 years experience in QC/QA is advantageous.
• Knowledge of GMP/GLP requirements and analytical method troubleshooting.

Responsibilities

• Support project flow through Right First-Time testing and schedule adherence.
• Execute Analytical Method Validation (AMV) activities per approved protocols.
• Perform analytical testing on trial samples and document results.
• Set up and test stability studies following CDC Product trial protocol.
• Ensure compliance with GMP, laboratory procedures, and quality standards.
• Support testing during weekends as needed.

Skills

HPLC

Dissolution testing

Analytical chemistry

Documentation

Team collaboration

Education

Bachelor's degree in Chemistry/Pharmaceutical Science/Analytical Science

Tools

Analytical instrumentation

Job description

Apply for QC Analyst (1 Year Fixed Term Contract) at Haleon in Kuala Lumpur, M14, MY. This Full time on site position offers great opportunities for career growth. Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity. Our trusted portfolio of brands – including Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum® – lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science. Now it’s time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose – to deliver better everyday health with humanity – at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture. Hi. We’re Haleon. A world-leading consumer healthcare company with exceptional category-leading brands – including Sensodyne, Centrum, Panadol, Otrivin. We have a clear purpose: to deliver better everyday health with humanity . For billions of people around the globe.

Other Key Responsibilities:

• To support smooth project flow through Right First-Time testing and schedule adherence.
• Execute Analytical Method Validation (AMV) activities in accordance with approved protocols.
• Perform analytical testing on trial samples and accurately document results.
• Perform stability study setup and testing following to CDC Product trial protocol.
• Ensure compliance with GMP, laboratory procedures, and quality standards.
Support project timelines through timely and accurate laboratory testing.
• To support testing during weekend on need basis

Why you?

We look for people who appreciate the importance of safety and quality and strive to continuously improve our performance and practices. We work in an open and transparent environment so you’ll be someone who treats others with respect and integrity – as you will be treated yourself. Ideally, we are looking for someone with : Bachelor's Degree or equivalent qualification in a relevant field such as Chemistry, Pharmaceutical Science, Analytical Science, or related scientific disciplines . Fresh graduates with strong academic achievements are encouraged to apply. Candidates with 1 to 3 years of experience in a Quality Control (QC) or Quality Assurance (QA) environment will have an added advantage. Knowledge of and familiarity with Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) requirements. Ability to troubleshoot analytical methods and laboratory instrumentation effectively. Hands-on experience with HPLC , D issolution testers , and other analytical laboratory equipment is preferred. Good interpersonal, communication, and stakeholder management skills, with the ability to collaborate effectively across teams. Self-motivated, independent, and able to demonstrate confidence, professionalism, and maturity in the workplace. Able to work under pressure and manage multiple priorities to meet tight project timelines.

Equal Opportunities Haleon are committed to mobilising our purpose in a way that represents the diverse consumers and communities who rely on our brands every day. It guides us in creating an inclusive culture, where different backgrounds and views are valued and respected – all in support of understanding and best serving the needs of our consumers and unleashing the full potential of our people. It’s important to us that Haleon is a place where all our employees feel they truly belong. During the application process, we may ask you to share some personal information, which is entirely voluntary. This information ensures we meet certain regulatory and reporting obligations and supports the development, refinement, and execution of our inclusion and belonging programmes that are open to all Haleon employees. The personal information you provide will be kept confidential, used only for legitimate business purposes, and will never be used in making any employment decisions, including hiring decisions.