Quality Control Analyst

Haleon; Jakarta Timur; On-site; IDR 100.000.000 - 200.000.000; Full time

Job summary

A global health-focused consumer company is seeking a Quality Control Analyst to ensure compliance and conduct analytical testing. The role involves analyzing samples and reporting data. Candidates should have vocational training in chemical analysis and at least 4 years of experience in the pharmaceutical industry. The position is a 1-year contract based in Jakarta, Indonesia, offering opportunities to advance in a dynamic environment.

Qualifications

• Minimum 4 years in pharmaceutical or associated industry.
• Good knowledge and understanding of pharmacopoeia expectations.
• Skillful to operate laboratory instrument related with the work assignment.

Responsibilities

• Conduct analytical development method testing effectively and efficiently.
• Responsible for the compliance of analytical methods to regulations.
• Collaborate with validation teams on method introductions.

Skills

Analytical testing

Knowledge of cGMP

Laboratory instrument operation

Quality assurance

Education

Vocational school for Chemical Analyst or associated science

Tools

Analytical instruments

Job description

Overview

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.

We are currently looking for Quality Control Analyst that will ensure the quality control testing related analytical development method are performed to GMP and company standards. This involves analyzing samples, recording, evaluating and reporting data using valid procedures with limited or no supervision.

This position is open for 1 year contract.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

Responsibilities

• Conduct analytical development method testing effectively and efficiently in compliance to valid analytical method protocol.
• Responsible for the availability of valid analytical method, specification and laboratory report for analysis purpose.
• Responsible for the compliance of analytical method and specification to current pharmacopeia monograph, Haleon and local regulation.
• Collaborate with validation to ensure validation activities (e.g. analytical method, process, cleaning, computerized system) are conducted as per agreed plans.
• Responsible for ensuring a consistent approach for the introduction of analytical methods for new products to the site, as well as effective transfer of methods for established products to other sites / 3rd parties.
• Comply and demonstrate aspects of EHS to daily work.

Why you?

Basic Qualifications:

• Vocational school for Chemical Analyst or associated science.
• Minimum 4 years in pharmaceutical or associated industry.

Preferred Qualifications:

• Understanding of basic manufacturing processes, laboratory activities and basic quality system.
• Good knowledge and understanding of pharmacopoeia expectations.
• Good knowledge of cGMPs and local regulatory requirements especially in good laboratory practices and good documentation practices.
• Good knowledge of the cGMP requirements as applied to an analytical laboratory.
• Good knowledge of of analytical / inspection techniques, precision and accuracy.
• Skillful to operate laboratory instrument related with the work assignment.
• Technical expertise in a broad range of analytical methodologies for testing API and/or drug products.

Job Posting End Date

Job Posting End Date: 2026-02-25

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.

Adjustment or Accommodations Request

If you require a reasonable adjustment or accommodation or other assistance to apply for a job at Haleon at any stage of the application process, please let your recruiter know by providing them with a description of specific adjustments you are requesting. We’ll provide all reasonable adjustments to support you throughout the recruitment process and treat all information you provide us in confidence.

Note to candidates

The Haleon recruitment team will contact you using a Haleon email account (@haleon.com). If you are not sure whether the email you received is from Haleon, please get in touch.