Senior Engineer, Validation

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

At Voyant Beauty, our people are the driving force behind everything we achieve.

We specialize in the development and manufacturing of beauty, personal care, OTC, and cosmetic products, partnering with leading brands and retailers to bring innovative ideas to life.

Our culture is rooted in teamwork, respect, and continuous growth — ensuring every individual’s contribution is valued and celebrated.

We’re currently seeking a Validation Engineer (also known as Process Validation Engineer, Equipment Validation Engineer, CQV Engineer, or Validation Specialist) to join our team.

This role is critical in ensuring compliance with cGMP, FDA, and industry quality standards through the validation of processes, cleaning methods, utilities, and equipment.

If you have experience in process validation, commissioning and qualification (CQV), or quality engineering within regulated industries such as pharmaceuticals, biotech, cosmetics, or medical devices, this could be the perfect opportunity to apply your expertise in a dynamic and growing environment.

  

•    Conduct Process and Cleaning Validations on any regulated products including Over-the Counter products and cosmetics 

•    Conduct all IQ/OQ qualifications on both new and existing equipment. 

•    Conduct all IQ/OQ/PQ qualifications on both new and existing systems such as USP Water System, compressed air etc. 

•    Assist with creating cleanout SOPs for cGMP and other products. 

•    Conduct validations where extensive engineering may be required. 

•    Advise engineering requirements needed to validate new Equipment especially Optical or Electronic/Computer controlled equipment under consideration. 

•    Write general SOPs when required. 

•    Conduct special engineering/testing activities when requested. 

•    Attend customer meeting/phone meetings when necessary. 

•    Provide advice to support departments on cGMP activities. 

•    Review of all pertinent documents as required. 

•    Maintain excellent documentation and records for audits and reviews. 

•    Develop standards and templates for Voyant Custom products and for specific customers 

•    Proficient in understanding analytical and micro test results / methods 

•    Able to assist in environmental monitoring testing with 3rd party labs 

•    Able to write validation protocols, interim and final reports 

•   Execute validations with limited supervisor 

•    Assist in internal and external audits 

•    Strong knowledge of cleaning validations 

•    Able to assist in investigations and QC lab functions

Qualifications 

•  Bachelor’s degree in mechanical engineering or related field of study. 

•  Experienced in cosmetics/personal care...