Validation Engineering Specialist in Eagan

Energy Jobline is the largest and fastest growing global Energy Job Board and Energy Hub. We have an audience reach of over 7 million energy professionals, 400,000+ monthly advertised global energy and engineering jobs, and work with the leading energy companies worldwide.

We focus on the Oil & Gas, Renewables, Engineering, Power, and Nuclear markets as well as emerging technologies in EV, Battery, and Fusion. We are committed to ensuring that we offer the most exciting career opportunities from around the world for our jobseekers.

Job DescriptionJob Description

HiFyve is hiring a Validation Engineering Specialist in the OTC and personal care industry in Eagan, MN!

Salary: $67K - $90K

Shift: Day Shift

Location: Eagan, MN

Position Overview:

A well-established manufacturer in the OTC and personal care space is hiring a Validation Engineering Specialist to support qualification and validation activities for regulated products, including skincare and sunscreen formulations. This role is ideal for a validation professional who enjoys hands-on work, cross-functional collaboration, and ensuring compliant, reliable manufacturing processes.

Key Responsibilities:

• Execute facility, utility, and equipment qualifications
• Support process validation and performance qualification (PQ/PPQ) activities
• Lead and support cleaning validation and computer system validation efforts
• Partner with Quality, Production, and Engineering teams on validation initiatives
• Support SOP updates, training, and validation documentation
• Assist with pFMEAs, process trials, pilot batches, and validation runs for new formulations
• Prepare validation reports, metrics, and project updates
• Ensure compliance with cGMP, FDA regulations, OTC monographs, and internal quality standards
• Support audits, risk assessments, corrective actions, and equipment qualification



Knowledge, Skills, and Abilities:

• Bachelor’s degree in Chemistry, Physical Sciences, or a related field
• 3+ years of validation experience in pharmaceutical and/or personal care manufacturing
• At least 1 year of experience in Rx or OTC manufacturing environments
• Working knowledge of equipment, utility, process, cleaning, and computer system validation
• Strong understanding of cGMP, FDA regulations, and OTC compliance requirements
• Ability to manage multiple validation projects and deadlines
• Strong documentation, communication, and cross-functional collaboration skills
• High attention to detail and a proactive, problem-solving mindset
• Lean Six Sigma Green Belt or higher ()
• Experience supporting new product introductions or formulation scale-up ()

If you are interested, please apply.

If you are interested in applying for this job please press the Apply Button and follow the application process. Energy Jobline wishes you the very best of luck in your next career move.