H

Engineer, Validation

Accepting applications

Herbalife · Lake Forest, CA

Full-Time Mid_senior Sicaiarmasicate
Posted
29 Apr
Category
Test
Experience
Mid_senior
Country
United States
Overview

Join an award-winning team at one of Orange County's Top Workplaces! Herbalife at Lake Forest has been recognized by the OC Register for our exceptional workplace culture, and we're looking for a dedicated Engineer, Validation to help us maintain our world-class standards.

ROLE AT A GLANCE:

This is your opportunity to play a critical role in ensuring the products that improve millions of lives around the world are manufactured with the highest level of quality, safety, and integrity.

The Validation Engineer is responsible for all equipment and process validation activities at Herbalife Innovation and Manufacturing site, with primary focus at the Lake Forest location. Execution of validation activities is done to state and federal regulatory requirements, Herbalife and/or other applicable regulations and standards. The Validation Engineer supports all projects required for the expansion and improvement of operations at the production facility and coordinates all validation activities and projects with departmental managers.

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.

Your technical expertise directly supports the team who help make our amazing products.

Qualifications

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.


Ready to bring your validation expertise to a company with real global impact? Apply today and become part of the Herbalife team.

At Herbalife, we value doing what’s right. We are proud to be an equal opportunity employer, making decisions without regard to race, color, religion, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected characteristic. We value diversity, strive for inclusivity, and believe the differences among our teammates is a key contributor to Herbalife’s ongoing success.

Herbalife offers a variety of benefits to eligible employees in the U.S. (limited to the 50 States and the District of Columbia), which includes Group Health Programs, other Voluntary Benefit Programs, and Paid Time Off. Group Health Programs include Medical, Dental, Vision, Health Savings Account (HSA), Flexible Spending Accounts (FSA), Basic Life/AD&D; Short-Term and Long-Term Disability and an Employee Assistance Program (EAP).

Other Voluntary Benefit Programs include a 401(k) plan, Wellness Incentive Program, Employee Stock Purchase Plan (ESPP), Supplemental Life/Critical Illness/Hospitalization/Accident Insurance, and Pet Insurance. Paid time off includes Company-observed U.S. Holidays, Floating Holidays, Vacation, Sick Time, a Volunteer Program, Paid Maternity and Paternity Leave, Bereavement Leave, Personal Leave and time off for voting.

If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please email your request to [email protected].

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