Validation Specialist

Hello. Were Haleon. A new world-leading consumer health company. Shaped by all who join us. Together we're improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands including Sensodyne, Panadol, Advil, Voltadol, Theraflu, Otrivin, and Centrum through a unique combination of deep human understanding and trusted science. What's more, we're achieving it in a company where we're in control, in an environment that we're co-creating, and a culture that's uniquely ours. Care to join us? It isn't a question.

With category-leading brands such as Sensodyne, Voltadol, and Centrum built on trusted science and human understanding, combined with our passion, knowledge, and expertise, we're uniquely placed to grow a strong, successful business.

This is an exciting time to join us and help shape the future. It's an opportunity to be part of something special.

About the role of Validation Specialist

Key responsibilities

Accountable for oversight, management, and delivery of all Validation Lifecycle components.

Ensures compliance with evolving expectations of Equipment and Facility C&Q, Process / Packaging validation, Cleaning validation, Continued Process validation (CPV), and Computer System validation.

Collaborates across Engineering, Quality, and Technical departments to ensure validation activities are completed on time and compliant with Haleon standards.

Prepares and maintains the site validation master plan (SVMP).

Maintains the site cleaning lifecycle process, assessing impacts of new products, processes, or changes, and coaches the Technical team to ensure validation demonstrates reproducibility and proper monitoring.

Leads and supports manufacturing process improvement projects.

Participates in Performance Centric Teams (PCT) and supports HAPS deployment.

Evaluates validation impact on change controls and manages compliance records including deviations, CAPAs, change controls, and events.

Supports investigations related to complaints, risk identification, and problem-solving to eliminate recurring issues.

Manages projects related to validation activities.

Qualifications and skills (Essential)

BS degree in engineering, industrial pharmacy, chemistry, or other scientific / pharmaceutical discipline.

Specialization in process and cleaning validation.

Minimum of 3 years of GMP-regulated technical experience in process and cleaning validation.

Proficiency in problem-solving, continuous improvement tools, and project management.

Experience in field or plant operations, implementing FDA and GMP regulations.

Ability to communicate effectively with staff, peers, and senior executives.

In-depth understanding of production forecasts and SAP systems.

Skills in problem-solving, SAP eBR, Serialization, Workday, Veeva, MyLearning, Office.

Fluent in English and Spanish.

Strong teamwork and communication skills, with the ability to inspire others.

Diversity, Equity, and Inclusion

At Haleon, we embrace our diverse workforce by creating an inclusive environment that celebrates unique perspectives, fosters curiosity, and promotes fair outcomes. We strive to create a workplace where everyone feels they belong and can thrive.

We support flexible working arrangements and encourage candidates to discuss opportunities with our hiring team.

Application process and accommodations

We invite you to share voluntary personal information to help us meet our diversity goals. All information is confidential and not accessible to hiring managers.

Haleon is an Equal Opportunity Employer. We provide reasonable accommodations upon request during the application process.

Required Experience

Unclear seniority level.

Key Skills

Python, SOC, Debugging, C / C++, FDA Regulations, Minitab, Technical Writing, GAMP, OS Kernels, Perl, cGMP, Manufacturing.

Employment Details

Type : Full-Time

Experience : [Specify years]

Vacancy : 1

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