QC Analyst (Fixed-Term Contract)

Haleon; Jakarta Pusat; On-site; IDR 66,960,000 - 100,440,000; Full time

Job summary

Haleon in Jakarta Timur seeks a Quality Control Analyst for a 12-month fixed-term contract. You will perform chemical/physical testing of materials and finished products, ensuring GMP compliance and proper documentation.

Responsibilities include testing, data recording, reagent control, calibration checks, and timely reporting of OOS results. Requires a chemical analyst background and strong teamwork and English communication.

Qualifications

• Vocational school for Chemical Analyst or associated science.
• 4 years in pharmaceutical or related industry.
• Good knowledge of analytical techniques and quality systems.

Responsibilities

• Conduct chemical and physical testing for raw materials and finished products in GMP-compliant manner.
• Record, store and report data with valid procedures and good documentation practices.
• Manage reagents, calibration records, and stock of analytical standards.
• Immediately report OOS results and deviations to Quality Control Lead.

Skills

MS Office

Good teamwork

Interpersonal skills

English communication

Education

Vocational school for Chemical Analyst

Tools

Laboratory instruments

Job description

## QC Analyst (Fixed-Term Contract)Apply: Indonesia - DKI Jakarta - Jakarta Timur: Full time: Posted Today: End Date: October 31, 2026 (25 days left to apply): 548563Welcome 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 12 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:**We are looking for professionals with these required skills to achieve our goals:* Vocational school for Chemical Analyst or associated science* 4 years in pharmaceutical or associated industry## ## Preferred Qualifications:If you have the following characteristics, it would be a plus:* 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.