Validation Lead

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.

Oversee and manage all site validation activities, ensuring compliance with regulatory and Haleon standards. This role leads cross‑departmental efforts to execute validation processes and maintain audit readiness, while developing the technical team and ensuring cleaning validation practices yield reliable, compliant results. This role will provide YOU the opportunity to lead key activities to progress YOUR career.

• Manages a team of Product and Process Engineers to support Product Lifecycle Management of products manufactured on site
• Accountable for oversight, management, and delivery of all Validation Lifecycle components
• Understands and ensures compliance to evolving expectations of:
  Equipment and Facility C&Q, Process/Packaging validation, cleaning validation, Continued Process validation (CPV), Analytical Method validation, and Computer System validation
• Collaborates across Engineering, Quality and Technical departments to ensure validation activities are completed on time and compliant to Haleon standards
• Ensures that the site can demonstrate system compliance to a regulatory auditor, (e.g., FDA, Health Canada, or ANVISA)
• Maintains site validation master plan (SVMP)
• As the site cleaning SME, maintains the site cleaning lifecycle process by assessing impact of new products, processes, or changes against the existing site cleaning matrix.
• Coaches and develops the Technical team to ensure that cleaning validation execution demonstrates that the process produces the expected results in a reproducible manner, and that proper monitoring is in place to ensure the processes remain in a validated state of control

This role is located onsite at our Lincoln, NE facility.

Basic Qualifications:

• BS degree in engineering, industrial pharmacy, chemistry, or other appropriate scientific or pharmaceutical discipline
• 5+ years of demonstrated experience in an FDA regulated technical role, with strong experience in cleaning validation

Preferred Qualifications:

• Able to effectively communicate and work with co-workers, management, and other departments

• 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

Haleon are committed to mobilising our purpose in a way that represents the diverse consumers and…