CM Site Operation Supervisor at Haleon

Yangzhou, Jiangsu, China -

Full Time

Start Date

Immediate

Expiry Date

02 Jul, 26

Salary

0.0

Posted On

03 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Assurance, Manufacturing Operations, Regulatory Compliance, cGMP, Process Monitoring, Root Cause Analysis, CAPA, Technical Troubleshooting, Data Integrity, ALCOA Principles, Internal Audits, Risk Management, SOP Compliance, Documentation, Intellectual Property Protection

Industry

Consumer Services

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. Key responsibilities: Scope of Accountability: Oversight of day-to-day manufacturing and quality operations at CMO sites. Real-time monitoring of processes to ensure compliance with Haleon policies and global regulatory standards. Acting as the first line of defense for IP protection and quality assurance. Operational Oversight & Compliance Conduct daily GEMBA walks across production, packaging, and dispensing areas to observe and verify compliance. Perform process confirmations and surprise spot checks to ensure SOPs and Haleon standards are followed. Monitor raw material dispensing and IPC checks, ensuring they are performed following the correct protocols and fully documented in compliance with Haleon standards. Validate laboratory testing protocols and ensure timely completion of quality checks. Oversee destruction of rejected or expired materials in accordance with Haleon policy and regulatory requirements. Ensure strict adherence to ALCOA principles (Attributable, Legible, Contemporaneous, Original, Accurate) in all documentation and data integrity practices. Quality Assurance & Risk Management Ensure operators and technicians consistently follow approved procedures. Identify and escalate deviations promptly; support root cause analysis and CAPA implementation. Contribute to internal audits and regulatory inspections, coordinate documentation and evidence. Protect Haleon’s intellectual property by enforcing confidentiality and security protocols at CMO sites. Continuous Improvement & Reporting Document all observations, findings, and corrective actions in a structured manner. Provide regular reports to Haleon Quality and Supply Chain leadership on compliance status and risk areas. Drive continuous improvement initiatives to enhance process reliability and reduce quality risks. Requirements: 3-5 years experience in various technical and quality assurance roles Breadth of knowledge and experience apply cGMPs and other regulations/guidance with an ability to interpret those in a fast-paced environment Operational excellent exposure Experience in technical troubleshooting, RCA and CAPA effectiveness Bachelor or master’s degree of Chemistry, Science, Biology in education Job Posting End Date 2026-04-30 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. 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.

Responsibilities

The supervisor will oversee day-to-day manufacturing and quality operations at CMO sites to ensure compliance with global regulatory standards. They are responsible for real-time process monitoring, conducting GEMBA walks, and managing quality assurance and risk mitigation activities.