Job Description

Hello. We\xe2\x80\x99re Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we\xe2\x80\x99re improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands \xe2\x80\x93 including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum \xe2\x80\x93 through a unique combination of deep human understanding and trusted science. What\xe2\x80\x99s more, we\xe2\x80\x99re achieving it in a company that we\xe2\x80\x99re in control of. In an environment that we\xe2\x80\x99re co-creating. And a culture that\xe2\x80\x99s uniquely ours. Care to join us. It isn\xe2\x80\x99t a question.With category leading brands such as Sensodyne, Voltaren and Centrum, built on trusted science and human understanding, and combined with our passion, knowledge and expertise, we\xe2\x80\x99re uniquely placed to do this and to grow a strong, successful business.This is an exciting time to join us and help shape the future. It\xe2\x80\x99s an opportunity to be part of something specialAbout the roleAccountable for implementation and maintenance of Quality Assurance procedures and systems to ensure compliance to ISO 13485, PIC/s and corporate policies.Role ResponsibilitiesGeneral Responsibilities for Operational Quality:

• To act as Quality liaison person during the shift operation at operational area including Production, Warehouse, QC Laboratory and Facilities area
• To advise on all aspects of GMP compliance and facilitating finished product release and assess the quality impact.
• To conduct In-process Quality Checks at the production floor as per SOP requirements (for packing operation).
• To be authorized as Authorised Person (AP) and review batch record completion and retain sample to ensure batch is produced in accordance with the procedure.
• To participate in on-line problems solving and conduct investigations as required.
• To involve as Quality Reviewer in Root Cause Analysis and Deviation as well as Rapid response (RR) Investigation at site.
• To support Product Complaint Investigation and Counterfeit Verification at site.
• To identify and manage the risk at respective Operational Quality scope and area.
• Product Reviewer for Periodic Product Review at site.
• To involve in audit preparation for Operational Quality section including Level 1 audit for areas of concern.

Role Specific Responsibility

• Work on shift pattern including weekend and PH.
• To verify In-process Quality Checks at the production floor as per SOP requirements during walkabout at both manufacturing and packing lines.

(*and not limited to the above as per assigned by line manager)Why you?Basic Qualifications:

• Degree in any field
• Experience in Quality and/or Production.

Preferred Qualifications:

• Degree in Science/ Pharmaceutical/ Technology

Preferably knowledgeable in Quality AssurancePreferably experienced in manufacturing and operational field Preferably familiar with GMP requirement and ALCOA+ principles. * Ability to understand and having technical knowledge in manufacturing and packing process, including GMP requirement.

• Minimum of 3-5 years of Operation and/or Quality Assurance experience.
• Technical knowledge and competency in manufacturing and packaging processes (preferred)
• Thorough knowledge of GMP and GLP (preferred)
• Familiarize with auditing (preferred)
• Conversant at Quality Document Control System (preferred)
• Skilled at technical report writing
• Willing to learn attitude
• Able to deliver training to small and / or large groups.
• Able to influence others (persuasiveness and assertiveness)

Location \xe2\x80\x93 this role is based in: Ulu Kelang/Ampang, Kuala LumpurThis position is a grade: 10Care to join us. Find out what life at Haleon is really like www.haleon.com/careers/At Haleon we embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives, generates curiosity to create unmatched understanding of each other, and promotes fair and equitable outcomes for everyone. We\'re striving to create a climate where we celebrate our diversity in all forms by treating each other with respect, listening to different viewpoints, supporting our communities, and creating a workplace where your authentic self belongs and thrives. We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.As you apply, we will ask you to share some personal information, which is entirely voluntary. We want to have an opportunity to consider a diverse pool of qualified candidates and this information will assist us in meeting that objective and in understanding how well we are doing against our inclusion and diversity ambitions. We would really appreciate it if you could take a few moments to complete it. Rest assured, Hiring Managers do not have access to this information and we will treat your information confidentially.Haleon is an Equal Opportunity Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, Haleon may be required to capture and report expenses Haleon incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure Haleon\xe2\x80\x99s compliance to all federal and state US Transparency requirements.

Haleon