Quality & Systems Compliance Manager

Location: New York

Quality & Systems Compliance Manager page is loaded## Quality & Systems Compliance Manager locations:
USA - New York - Oak Hilltime type:
Full time posted on:
Posted Todaytime left to apply:
End Date:
February 28, 2026 (15 days left to apply) job requisition :
540040

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.
** About the role
*** The Quality System Manager ensures the site has robust efficient Quality System to maintain and continuously improve compliance with the regulatory requirements of all markets to which the site supplies products.  Critical in providing compliance governance of site-wide organizational systems critical to maintain business operations, including enterprise resource planning (ERP), Automation, Electronic Batch Records (E ) and Laboratory Management Systems (LIMS) etc.
*** Role Responsibilities
*** Ensures site Quality Systems are robust, effective, and compliant with regulatory requirements of all markets to which the site supplies products, especially in the following programs and activities:*
* * Change Control program oversight including the interphase with Regulatory Affairs and related functions - Review and approval of process, product and facility change proposals, including trending and assessment of impact of changes over time.*
* * Document Management - Management of the documentation lifecycle process including procedures, Release specifications and laboratory methodology.*
* * QA Validation Oversight - Review and approval of Site Validation Master Plan, all product and non-product validation plans and reports including facilities, cleaning, equipment, CSV and QC equipment’s.*
* * Periodic Product Review Oversight – Reviews and approval of periodic product reviews reports on a timely manner following the annual schedule.*
* * Quality Standards and Policies implementation*
* * Ensure Supplier Quality practices are executed throughout the functional roles within the organization.*
* * Leads efforts is remediating critical supplier non-conformances.*
* * Actively partners with senior stakeholders at site to drive CI culture and partnership with key suppliers.*
* * Material Certification Process, Product Components and Finished Products Risk Assessments (BSE/TSE, GMO, Allergen, Residual Solvents, etc.)*
* * Data System aligned to software application of QC equipment, automation, and standalone equipment.*
* * Ensure Haleon Consumer Healthcare Quality standards are met while delivering robust oversight of Product Lifecycle*
* * Provides guidance and direction to all-training practices at site to ensure quality compliance is met*
* * Constantly challenges the effectiveness and simplicity of the Quality Systems to ensure efficiency and user-friendliness.*
* * Support the goals and objectives of the site Quality Unit and the site.*
* * Network and liaise as appropriate with other Quality professionals within the wider Quality team and in their support of campus operations.*
* * Participates in Inspection Readiness and DI Gembas*
* * Supports QA operating budgets for headcount & capital expenditures
**
* Basic Qualifications:

**
* * Bachelor’s degree in engineering (Chemical, Mechanical, Electrical or a related field scientific field)*
* * 5+ years' experience in a process, manufacturing, project, or R&D engineering position*
* * Experience in Pharmaceutical/FMCG or other…