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Product and Process Engineer

Job in Lincoln, Lancaster County, Nebraska, 68511, USA
Listing for: Haleon
Full Time position
Listed on 2025-12-15
Job specializations:
  • Engineering
    Process Engineer, Quality Engineering, Chemical Engineer, Manufacturing Engineer
Job Description & How to Apply Below
Product and Process Engineer page is loaded## Product and Process Engineer locations:
USA - Nebraska - Lincoln time type:
Full time posted on:
Posted Todaytime left to apply:
End Date:
January 11, 2026 (29 days left to apply) job requisition :
538093

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
** Product and Process Engineer
** is part of a team responsible for maintaining comprehensive product and process knowledge at the site. It supports validated manufacturing through collaboration with cross-functional groups, execution of process and cleaning validations, ongoing risk assessments, and alignment on technical changes to ensure product quality and regulatory compliance.
*** Role Responsibilities
*** Recognized as the principal point of contact for all aspects of current and previous knowledge on the product(s), performance and end to end process, including critical quality attributes (CQAs) and critical process parameters (CPPs). Accountable at site level for maintaining this knowledge and sharing on site and globally as appropriate.
* Liaise with Regional and Global Technical, as well as other site functions such as QA, QC, Engineering, and Operations to ensure that proper controls are established and maintained for products to be manufactured in a validated state of control.
* Implement and maintain continued process verification (CPV), as appropriate, for determined products and processes on site.  Incorporate data trending and statistical analysis to verify that processes remain in a validated state of control, and to proactively identify trends which may provide risk to the product.
* Maintains and periodically reviews product control strategies (PCS) and technical risk assessments (TRA) as required.
* Provide all necessary information to develop and execute process validation, working across multiple functions to collect the appropriate inputs for validation protocols and authoring validation reports. Validates the manufacturing and packaging process parameters necessary to assure product quality and incorporates this into the PCS.
* Lead or contributes to, as required, change controls impacting products or manufacturing processes. Ensure alignment of timelines and activities required for technical changes, product transfers, major deviations, and investigations.
* Performs risk assessments on cleaning processes, as required for new products, processes, or materials introduced to the site, and ensuring appropriate validation is implemented.  This includes HBEL, MACO, residual solvent calculations, and other assessments to support cleaning validation needs.  Develops and works with Operations to execute protocols for cleaning validation, and issues validation reports.
*
* Basic Qualifications:

*** A minimum of a Bachelor’s Degree in Chemical Engineering, Chemistry or other related Engineering discipline is required.
*
* Preferred Qualifications:

*** A background in the pharma or animal health industries is a plus.
* Experience with Statistica or similar statistical/data analysis program would be beneficial.
* A minimum of 3 years of experience with process validation and/or product stewardship is a plus.

Location – this role is based in:
Lincoln, Nebraska.  This is not a remote role.##
** Benefits
* * Haleon offers a robust Total Reward package that consists of…
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