Regulatory and Compliance Supervisor

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 looking for a Regulatory Compliance Supervisor to help strengthen quality and regulatory compliance at our Haleon Pulogadung site in Indonesia. In this role, you will support the implementation of our Quality Management System, ensure regulatory conformance, and provide oversight across key quality processes including Periodic Product Review, Technical Terms of Supply, change control, CAPA, product complaints, documentation lifecycle, and regulatory submissions.

A day in the life

Role Responsibilities:

  • You will assess Quality Management System documents, ensure alignment with global QMS requirements, and support effective site implementation.
  • You will prepare periodic product review reports for products manufactured at Haleon Pulogadung Site, Indonesia.
  • You will manage Technical Terms of Supply and quality agreements for marketed products handled by the site.
  • You will own the site change control process, ensuring changes are managed effectively and in compliance with applicable standards.
  • You will oversee the CAPA system and help drive effective corrective and preventive actions across the site.
  • You will provide oversight of the documentation lifecycle for compliance-owned documents.
  • You will prepare regulatory submission dossiers and ensure products remain compliant with regulations in the markets where they are sold.

Why you?

Basic Qualifications:

We are looking for someone with:

  • Pharmacist qualification, with direct experience in quality systems, validation, documentation, and compliance.
  • 1–2 years of experience in quality operations or quality assurance, ideally within a regulated manufacturing environment.
  • Working knowledge of GMP and regulatory compliance requirements.

Preferred Qualifications:

It would be a plus if you also have:

  • 1–3 years of experience in the pharmaceutical industry.
  • Strong written communication, organizational, and computer skills.
  • Confidence working with peers, team members, and senior stakeholders in a multidisciplinary environment.

Job Posting End Date

2026-08-01

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.