Global Product Owner

Haleon; New Jersey; Hybrid; USD 141,000 - 194,000; Full time

Benefits offered by this job

401(k) plan

Tuition reimbursement

Paid parental leave

Healthcare coverage for you and family

Discretionary bonus

Job summary

Haleon in Warren, NJ is seeking an experienced professional to own Product Quality Lifecycle management, including TRB escalation, root cause analysis, and change control. You will ensure Quality by Design in tech transfers from R&D to Supply Chain, driving improvements in product quality, cost and efficiency.

The role requires a Bachelor’s degree in science or engineering and 10 years of experience in consumer products, with strong GMP knowledge and regulatory familiarity.

Qualifications

• Bachelor’s degree in Science, Engineering, Pharmacy or related field.
• 10 years of technical experience in consumer products.
• Experience with Change Control, Deviation, CAPA and validation reports.
• Understanding of GMPs and regulatory requirements.

Responsibilities

• Ensures Product Quality Lifecycle management across products, including risk assessment and control strategies.
• Leads root cause analyses for investigations and product deviations in collaboration with QA and sites/CMOs.
• Evaluates new raw material suppliers with cross-functional teams and data interpretation.
• Provides technical justification to Health Authorities on global brands when required.
• Ensures compliance with written procedures and documents, and supports technology transfer with Quality by Design.

Skills

Quality systems

GMP knowledge

Regulatory compliance

Project management

Quality by Design

Stakeholder management

Education

Bachelor’s degree in Science/Engineering/Pharmacy

Master’s or PhD (preferred)

Tools

PMP Certification

Agile

Program Management

Job 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.

Role Responsibilities

Ensures that all aspects of Product Quality Lifecycle management are applied to the product(s) including a current Technical Risk Assessment, Product Control Strategy. Ensures a data driven continuous improvement program is in place for the dose forms/ products driving quality, cost and efficiency improvements. Proactively analyzes manufacturing, analytical, and stability performance trends, escalates significant findings to the TRB, and recommends continuous improvements. Is involved as required in the assessment and management of all aspects of post-approval change to ensure that product quality is maintained, and the appropriate change controls are in place. Provides technical leadership and input into root cause analyses to support complex investigations and resolution of product complaints and product deviations and investigations, in conjunction with QA and sites/CMOs. Assesses new raw material suppliers and work with Material Science and procurement teams on the interpretation of data to approve new alternative raw material suppliers. Provides technical justification with high-quality standards to Health Authorities on global brands when required and linked to product lifecycle management and/or maintenance project. Ensures all work by the team is conducted in accordance with written procedures (e.g. quality and safety), methods & batch documents, etc. Produces, contributes, or approves, departmental quality documentation (including SOP's, batch documentation, manufacturing protocols & reports, product specifications & development reports). Provides technical leadership during technology transfer of products into Supply Chain from R&D and out to other sites ensuring Quality by Design principles are applied and a robust, well understood process is transferred with a well-defined and appropriate Product Control Strategy. Provides technical product advice and training to site product owners and key stakeholders ensuring that sites have appropriate product knowledge and training to fully execute the Product Control Strategies.

Basic Qualifications

• Bachelor’s degree in Science, Engineering Pharmacy or related science discipline.
• 10 years of technical experience in consumer products.
• Product Lifecycle Management activities (Quality Events- Change Control, Deviation, CAPA’s, trial and validation reports author/reviewer/approver as appropriate, risk assessment author/reviewer/approver as appropriate), understanding of the auditing world.
• Good knowledge of product manufacturing processes including unit operation understanding, device/packaging processes, plant equipment and analytical testing.
• Previous experience in the development of conventional and potentially novel formulation dosage forms.
• Thorough understanding of Drug and Food GMPs as relevant to Haleon products as well as familiar with FDA, European and global regularity requirements, such as ICH Excellent understanding of scientific and commercial aspects of Consumer Healthcare industry

Preferred Qualifications

• Master’s or PhD.
• PMP, Agile, Program Management or Portfolio Management certifications.
• Previous Oral Health category experience.
• Strong business leadership and commercial acumen.
• Extensive project and portfolio management experience in complex matrix organizations.
• Ability to connect business objectives, technical possibilities and operational execution.
• Ability to influence without authority and manage executive stakeholders effectively.
• Expertise in governance, stage-gate management, risk management and change control.
• Track record of coaching and mentoring scientists and peers to build strong collaborative teams working in a high-performance environment in a culture that values scientific rigor and empowerment.
• External communication and/or network with regulators, external collaborators and/or scientific experts where needed.
• Effective relationship building, influencing and organizational and project management skills. Good oral and written communication skills at all levels within the organization; strong technical writing capability
• Proficient in Medical Device regulation knowledge relevant to project delivery.
• Experienced in negotiating and agreeing timelines and milestones with sponsors/ business partners and continually monitoring progress to ensure timely delivery.
• Deep understanding of Quality of Design (QbD), Operational Excellence (OE) and Value Engineering/ Design to Value.
• Demonstrated a sense of curiosity and appetite to learn by themselves.
• Site experience highly desired for practical application of the above.
• Operational experience with the ability to ideate and execute technical changes that drive growth and productivity.

Location

This is a hybrid position based in Warren, NJ, requiring on-site presence 3 days per week. The Salary Range for this role is $141,305 – 194,294 + an 18% annual target bonus.

Benefits

Haleon offers a robust Total Reward package that consists of competitive pay and a comprehensive benefits program. This includes a generous 401(k) plan, tuition reimbursement and time off programs including 6 months paid parental leave. On day one, you are eligible for benefits, including our healthcare programs where the company pays for the majority of your medical coverage for you and your family. We also offer the opportunity to receive a discretionary bonus based on the achievement of key business performance and other incentive/recognition programs as part of the offering.

Job Posting End Date

2026-10-14

Equal Opportunities

Haleon is 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. 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’s compliance to all federal and state US Transparency requirements.

Accommodation Requests

If you require a reasonable accommodation or other assistance to apply for a job at Haleon at any stage of the application process, please contact us by sending an email to [e-mail]. Please include the following in your email: Use subject line: ‘HaleonCareers:Job Accommodation Request’ Your Name and contact information Requisition ID and Job Title you are interested in Location of Requisition (city/state or province/country) Description of specific accommodation you are requesting Please note: Resumes, CVs, or other requests outside of accommodation support submitted to this email box will not be accepted.