Engineer, Validation

In this role, you will be empowered to take ownership, drive meaningful improvements, and be recognized as a trusted technical authority across the organization

HOW YOU’LL MAKE AN IMPACT: 

Every validation you complete helps ensure that a product meeting the highest quality standards reaches someone who depends on it. Here's how you'll do that day to day:

• Facilitates validation/qualification projects (planning, scheduling, execution, project reports, etc.).
• Creates validation protocols and summary reports in compliance with Herbalife standards and/or government regulations. This includes investigating and resolving protocol deviations in a timely manner.
• Coordinates change control and equipment-related changes (this includes providing assessment and feedback regarding change requests for equipment, facility, process modifications, etc.).
• Maintains SOPs related to validation/qualification (i.e. validation master plans, validation templates) and update them, as required, to meet current standards.
• Acts as back-up for management of the Global Environmental Monitoring (EM) program, which includes acting as an administrator for the associated Vaisala viewLinc application and working with temperature & humidity data loggers.
• Additional duties as assigned.

TEAM DYNAMICS:  

You'll be joining a collaborative, passionate team that values expertise, mutual respect, and a shared drive to get it right. Your voice matters here — your insights and technical recommendations will directly shape how we operate.

• Be able to work effectively with interdisciplinary departments to meet project deadlines and serve as a validation authority consulting with Engineering, Operations, and Quality.

LEADERSHIP AND SUPERVISORY RESPONSIBILITIES: 

Not applicable for this position.

Experience

We're looking for someone who brings real-world GMP expertise and is ready to make an immediate impact:

• 3-5 years of validation/qualification and process engineering experience in a GMP environment.
• 5+ years of experience in Good Manufacturing Practices and Good Documentation Practices.
• Experience in food, pharmaceutical and/or medical device process development.

QUALIFICATIONS FOR SUCCESS: 

Education

• Bachelor of Science in Chemistry or field of Engineering 

Skills/Certifications 

• Strong technical writing skills. Detailed knowledge of grammar, spelling, punctuation, and the fundamentals of technical GMP documentation.
• Strong mechanical aptitude and process knowledge. Ability to work independently with minimal supervision.
• Knowledge of PLC and automated controls qualification.
• Knowledge of qualification fundamentals and requirements for powder and liquid handling, processing, and packaging.
• Basic experience with equipment cleaning and computer systems validation methodologies is a plus.
• Experience in electronic validation systems is preferred but not required.
• Openness to learning skills outside of validation but is required for the expansion and improvement of operations at the production facility.

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