QC Analyst (8-month Fixed Term Contract)

Haleon plc.; Jakarta Pusat; On-site; IDR 60,000,000 - 100,000,000; Part time

Job summary

Haleon plc. is seeking a Quality Control Analyst for our manufacturing site in Jakarta Timur. You will ensure stability and finished product testing adheres to GMP and internal standards, analyzing samples and reporting data with minimal supervision.

Responsibilities include performing analytical testing, maintaining documentation, and ensuring instrument calibration and reagents are properly managed. This is a fixed-term contract role with potential for extension.

Qualifications

• Proven ability to perform chemical and physical testing per validated methods.
• Maintains accurate, compliant lab records and reports.
• Familiarity with cGMPs and laboratory documentation practices.

Responsibilities

• Conduct chemical and physical testing for raw materials according to testing plans and record results in lab reports.
• Perform stock opname and manage analytical working standards.
• Immediately report OOS results and deviations to Quality Control Lead.
• Record, store, inspect and destroy raw material samples according to SOPs.
• Monitor reagent stock and calibration dates; notify if expired or out of stock.
• Ensure data integrity and Good Documentation Practice across GxP activities.
• Maintain cleanliness of glassware, instruments, and work areas in the QC lab.

Skills

Analytical techniques

Documentation & data integrity

Quality systems understanding

English communication

MS Office proficiency

Laboratory instrumentation

Education

Vocational school in Chemical Analysis or related science

Tools

MS Office

Laboratory instruments

Job description

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 now looking for Quality Control Analyst to be based in our manufacturing site in Jakarta Timur.

As Quality Control Analyst, you will be responsible to ensure that the Quality Control testing of stability and finished product samples are performed to GMP and company standards. This involves analyzing samples, recording, evaluating and reporting data using valid procedures with limited or no supervision. Other duties may be assigned on discretionary basis as required by new developments or changes the role. This position is open for 8 months contract.

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

• Conduct chemical and physical testing for raw material effectively and efficiently in compliance to valid analytical method and record the results in laboratory report, as per testing plan prepared by Quality Control Lead.
• Conduct stock opname and management of analytical working standard.
• Immediately report any OOS results and deviations during the analysis in Quality Control Lab to Quality Control Lead.
• Record, store, inspect and destroy raw material samples.
• Control the preparation, use, storage and expiration date of the reagent and reference standard used in the testing process and ensure it is used in accordance with a valid procedure.
• Record the use of reagent and reference standard and notify Quality Control Lab Support or Reference Standard Responsible Person, if any reagent or reference standard is out of stock or expired.
• Check the date of calibration of instrument in the Quality Control Laboratory before use, record its use and report to Quality Control Lead if any nonconformance is found.
• Ensure Good Documentation Practice and data integrity is always shown on all GxP activities.
• Maintain the cleanliness of glassware and other instruments and work areas in the Quality Control laboratory.

Why you?

Basic Qualifications:

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

Preferred Qualifications:

• Understanding of basic manufacturing processes, laboratory activities and basic quality system
• Good knowledge of analytical/ inspection techniques, precision and accuracy
• Good knowledge of cGMPs and local regulatory requirements especially in good laboratory practices and good documentation practices.
• Skillful to operate laboratory instrument related with the work assignment.
• Good knowledge of troubleshooting analytical problems.
• Able to use MS office and internet.
• Able to have basic communication in English both verbal and written.
• Good team work and interpersonal skills.
• Result oriented, good reporting skill, strong analytical and numerical skills.

Job Posting End Date

2026-11-05

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.