QC SLIMS Project Officer (12-month Fixed Term Contract)

Haleon; Jakarta Timur; On-site; IDR 120,000,000 - 180,000,000; Full time

Job summary

Haleon is seeking a QC SLIMS Project Officer for a 12-month fixed-term contract to drive LIMS implementation at the Jakarta Timur site. You will work with the Analytical Development Lead to ensure on-time delivery, bridging laboratory operations, IT, and quality within a GMP framework.

The role requires a background in pharmacy, chemistry, or computer science and at least one year in pharma or related industries, with strong analytical and troubleshooting skills and a proactive, collaborative

Qualifications

• Pharmacist / Chemistry/ Computer Science, or other relevant scientific/technical disciplines.
• At least one year of experience in the pharmaceutical or an associated industry.
• Understanding of basic manufacturing processes, laboratory activities and system fundamentals.
• Knowledge of cGMP requirements as they apply to an analytic laboratory.
• Knowledge of analytical and inspection techniques, including precision and accuracy.
• Knowledge of how to troubleshoot analytical problems.
• Proficiency in Microsoft Office and internet use.
• The ability to make sound decisions based on scientific data.
• The ability to analyse data, clearly summarise findings and present conclusions.
• Strong teamwork and interpersonal skills.

Responsibilities

• You’ll support LIMS implementation from requirements gathering and configuration through testing, deployment and post-go-live support.
• You’ll gather laboratory business requirements and translate them into system requirements and appropriate LIMS configurations.
• You’ll help configure and verify laboratory workflows in LIMS.
• You’ll collaborate with laboratory users and relevant stakeholders to resolve system and process issues.
• You’ll support Computerized System Validation (CSV) activities in line with applicable GxP and site requirements.
• You’ll prepare and/or execute validation documentation, including USP, GxP risk assessments, Validation Plans and PQ protocols.
• You’ll execute test scripts and maintain objective evidence to demonstrate that the configured system performs as intended.

Skills

Pharmacist / Chemistry / Computer Sci

1+ year pharma/related industry exp

Job description

QC SLIMS Project Officer (12-month Fixed Term Contract)

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 Project Officer for SLIMS to be based in our manufacturing site inJakarta Timur.

As our Quality Control Project Officer for SLIMS, you’ll support the Analytical Development Lead in developing and implementing SLIMS at our Pulogadung site in Jakarta Timur. You’ll help keep the project on track for on-time delivery, working at the intersection of laboratory operations, technology and quality. This position is open for 12-month contract.

What you’ll do

• You’ll support LIMS implementation from requirements gathering and configuration through testing, deployment and post-go-live support.
• You’ll gather laboratory business requirements and translate them into system requirements and appropriate LIMS configurations.
• You’ll help configure and verify laboratory workflows in LIMS.
• You’ll collaborate with laboratory users and relevant stakeholders to resolve system and process issues.
• You’ll support Computerized System Validation (CSV) activities in line with applicable GxP and site requirements.
• You’ll prepare and/or execute validation documentation, including USP, GxP risk assessments, Validation Plans and PQ protocols.
• You’ll execute test scripts and maintain objective evidence to demonstrate that the configured system performs as intended.

Why you?

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

• Pharmacist / Chemistry/ Computer Science, or other relevant scientific/technical disciplines
• At least one year of experience in the pharmaceutical or an associated industry.

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

• Understanding of basic manufacturing processes, laboratory activities and system fundamentals.
• Knowledge of cGMP requirements as they apply to an analytical laboratory.
• Knowledge of analytical and inspection techniques, including precision and accuracy.
• Knowledge of how to troubleshoot analytical problems.
• Proficiency in Microsoft Office and internet use.
• The ability to make sound decisions based on scientific data.
• The ability to analyse data, clearly summarise findings and present conclusions.
• Strong teamwork and interpersonal skills.

Job Posting End Date

2026-12-02

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.