Validation Lead
- Location
- Lincoln, NE
- Listed
- 13 days ago
About the role
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.
Job Posting
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. These responsibilities include some of the following:
- 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
Basic Qualifications
We are looking for professionals with these required skills to achieve our goals:
- 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
If you have the following characteristics, it would be a plus
- Able to effectively communicate and work with co-workers, management, and other departments
This role is located onsite at our Lincoln, NE facility.
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
- 2026-11-23
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.
Note to candidates
The Haleon recruitment team will contact you using a Haleon email account (@haleon.com). If you are not sure whether the email you received is from Haleon, please get in touch.
Equal opportunity and legal notices
Haleon are 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.
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. Please include the following in your email:
- Your Name and contact information
- Requisition ID and Job Title you are interested in
- Location of Requisition (city/state or province/country)
From GSK nch's careers page, first listed on Rolev.ai on October 28, 2026. Rolev.ai is not the employer.
How Rolev.ai helps with this application
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Common questions
Where is the Validation Lead job at GSK nch located?
This Validation Lead position at GSK nch is located in Lincoln, NE. Always check GSK nch's application page for specific state eligibility or relocation policies.
How do I apply for the Validation Lead position at GSK nch?
This listing links directly to GSK nch's Workday application page. You can apply directly on GSK nch's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.