Engineer, Validation

“Applicants must be legally authorized to work in the United States without the need for sponsorship now or in the future.”

Voyant Beauty believes our people are more than just employees; they’re the driving force behind everything we achieve.

Our culture fosters teamwork, respect, and camaraderie, ensuring that every individual’s contribution is valued and celebrated.

We invest in their growth, providing opportunities for development and advancement within our dynamic team. 

Voyant Beauty is a company that specializes in the development and manufacturing, of beauty, personal and home care products.

We work with various brands, retailers, and businesses to create customer formulations and products tailored to their needs.

This can include skincare, haircare, bath and body products, fragrances, and more.

Essentially, Voyant Beauty serves as a one-stop-shop for companies looking to bring their beauty and personal care product ideas to life.

Safety is a core value at Voyant Beauty.

We prioritize the well-being of our team members, ensuring a safe and secure environment where everyone can thrive and excel.

If you’re seeking to be part of a team where your talents are valued, your safety is paramount, and your efforts contribute to meaningful change, then Voyant Beauty is the place for you.

Come join us and be a part of our journey.

A Brief Overview

The Validation Engineer is responsible for planning, executing, and documenting validation activities to ensure compliance with cGMP regulations and company quality standards.

This includes process, cleaning, equipment, and utility system qualifications for OTC products, cosmetics, and regulated systems.

The Validation Engineer collaborates closely with Engineering, Quality Assurance, and Operations to ensure that all validation activities meet regulatory and internal requirements and supports audits and investigations with proper documentation and technical expertise.

What you will do


* Review and approve validation protocols (IQ/OQ/PQ) for equipment, manufacturing processes, and cleaning procedures.

Develop template protocols, interim, and review final reports for new and existing systems, including USP water and compressed air systems.


* Write, review, and maintain SOPs, validation protocols, and technical documentation to ensure audit readiness and consistency.

Develop standards and templates for custom and regulated products.


* Advise on engineering and equipment requirements for validation, especially electronic/computer-controlled systems.

Assist in the creation of cleanout SOPs and perform engineering testing as needed.


* Participate in internal and external audits.

Maintain validation documentation for inspections and provide subject matter expertise on cGMP activities.


* Attend customer and cross-departmental meetings.

Support departments with technical insight on validation and compliance-related concerns.


* Assist with environmental monitoring ...