About the Role
We are seeking a Manufacturing Professional to drive Quality Management System improvement and simplification for their local region while collaborating with Quality Managers globally. As a LOC Quality Manager, you will ensure effective oversight of the Quality Management System (QMS) in your local region, meeting regulatory and customer expectations by harmonizing quality standards, simplifying processes, and driving compliance and efficiency.
Responsibilities
- Manage regional Local Operating Company (LOC) quality governance and risk management.
- Oversee Regional LOC Quality Performance Management (QPM) and Improvement, including organizing the Regional LOC Performance Management Forum.
- Monitor LOC Quality performance and assure the effectiveness of LOC quality processes.
- Lead projects and drive quality initiatives across LOCs in the region to improve quality compliance and efficiency.
- Own and implement Regional LOC Quality System and Processes.
- Oversee LOC QMS implementation through a program of quality standard harmonization.
- Serve as the Regional LOC QMS point of contact.
- Conduct audits to provide quality assurance and identify areas for improvement.
- Oversee quality performance for local 3rd party Service Providers.
- Harmonize LOC Quality ways of working with key distributors to drive standardization and efficiency.
- Partner with Supply Chain and LOC Quality to ensure significant 3rd party related risks are appropriately escalated and mitigated.
- Collaborate with other Regional LOC Quality, Regional Regulatory, and Regional Supply Chain teams to promote sharing and learning.
Requirements
- Bachelor’s Degree in Pharmacy, Science, or an engineering discipline, OR equivalent level of knowledge, understanding and hands-on experience of Good Manufacturing Practices in the pharmaceutical environment.
- 5 years of Manufacturing/Quality experience in the Pharmaceutical industry.
- Experience with the application of Quality Systems in manufacturing, warehousing, and distribution.
- Ability to work independently and prioritize workload.
- Excellent oral and written communication skills.
- Strong interpersonal skills with an ability to enable and drive change.
- Problem identification and solving skills.
- Experience of working with multi-functional teams.
Skills
- Quality Management System (QMS)
- Risk Management
- Quality Performance Management
- Quality Compliance
- Process Improvement
- Auditing
- Supply Chain Collaboration
- Regulatory Compliance
- Communication Skills
- Interpersonal Skills
- Problem Solving
Location
- Local region
Work Type
- Full-time
Experience Level
- 5 years of Manufacturing/Quality experience
Education Level
- Bachelor’s Degree in Pharmacy, Science, or an engineering discipline
- Equivalent level of knowledge, understanding and hands-on experience of Good Manufacturing Practices
About the Company
- Haleon is a purpose-driven, world-class consumer company focused on everyday health.
- Our trusted brands include Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum®.
- We combine deep human understanding with trusted science.
- Our Win as One strategy places our purpose – to deliver better everyday health with humanity – at the heart of everything we do.
- We foster an agile, performance-focused culture.
Equal Opportunity
- Haleon is committed to creating an inclusive culture where diverse backgrounds and views are valued and respected.
- We aim for Haleon to be a place where all employees feel they truly belong.
- Voluntary personal information may be collected to meet regulatory obligations and support inclusion and belonging programs.
- Personal information provided will be kept confidential, used only for legitimate business purposes, and will not influence employment decisions.
- Reasonable adjustments or accommodations are available upon request throughout the application process.
