Senior Validation Engineer, L'Oreal Operations

L'Oreal USA, Inc; North Little Rock (AR); On-site; USD 110,000 - 160,000; Full time

Benefits offered by this job

Medical coverage

Dental coverage

Vision coverage

401K plan

Pension plan

Flexible time off

Paid holidays

Vacation program

Shop discount

Mobile allowance

L&D access

Mentorship programs

Wellness programs

Job summary

L'Oréal USA, Inc. in North Little Rock, AR seeks a Sr. Engineer, Validation to lead validation design, execution, and documentation for equipment and lines.

You will mentor junior engineers and drive continuous improvement in a regulated manufacturing setting. The role requires 5-7 years CQV experience, IQ/OQ/PQ protocol authoring, GMP/ISO 22716 knowledge, and strong analytical writing. Collaboration with Engineering, Production, QA is essential, with audit-ready documentation maintained for

Qualifications

• Bachelor's degree in Chemical Engineering, Mechanical Engineering, or related field.
• 5-7 years manufacturing CQV experience in cosmetics/pharma acceptable.
• Proven authoring and executing IQ/OQ/PQ protocols for equipment and utility systems.
• Strong GMP/ISO 22716 and FDA knowledge and sanitary design principles.
• Experience validating PLC/SCADA systems and cleaning validation.
• Excellent technical writing, analytical, and problem-solving skills.
• Ability to lead cross-functional projects and mentor staff.

Responsibilities

• Lead design, execution, and documentation of validation protocols (IQ/OQ/PQ) for equipment, lines, and utilities.
• Mentor junior engineers; drive continuous improvement across the facility.
• Maintain audit-ready validation documentation and support inspections.
• Collaborate with Engineering, Production, Formulation, and QA for tech transfers.
• Manage multiple validation projects in a fast-paced manufacturing environment.

Skills

CQV experience

IQ/OQ/PQ protocols

GMP ISO 22716

Statistical analysis

Leadership/mentoring

Regulatory knowledge

Education

Bachelor's degree in Chemical/Mechanical Engineering or related

Tools

SCADA

PLC

Job description

Job Title: Sr Engineer, Validation

Location:

North Little Rock, AR

Reports To:

Manager - Quality Engineering

Who We Are:

For more than a century, L'Oreal has devoted its energy, innovation, and scientific excellence solely to one business: Beauty. Our goal is to offer each and every person around the world the best of beauty in terms of quality, efficacy, safety, sincerity and responsibility to satisfy all beauty needs and desires in their infinite diversity.

At L'Oreal Operations, we create innovative, inclusive, and sustainable beauty together with our business partners by designing, developing, sourcing, manufacturing, and distributing over 6 billion products globally every year. We support over 36 brands across four L'Oreal divisions. We are consumer-oriented, and we act responsibly all along the value chain.

What You Will Do:

The Sr. Engineer of Validation is responsible for leading the design, execution, and documentation of validation protocols (IQ/OQ/PQ) for new and existing equipment, manufacturing lines, automation systems, and cleaning processes. This role brings robust technical expertise in commissioning, qualification, and validation (CQV) within a regulated environment, along with strong leadership skills to mentor junior engineers and drive continuous improvement across our production facility.

What We Are Looking For:

• Bachelor's degree in Chemical Engineering, Mechanical Engineering, Bioengineering, Chemistry, or a related scientific/technical discipline required.
• 5-7 years of manufacturing experience (experience in commissioning, qualification, and validation (CQV) within the cosmetics, pharmaceutical, medical device, or personal care manufacturing industries preferred).
• Proven track record authoring and executing IQ/OQ/PQ protocols for manufacturing equipment (e.g., compounding vessels, filling lines, packaging equipment) and utility systems.
• Deep understanding of Good Manufacturing Practices (GMP), ISO 22716, FDA regulations, and sanitary design principles.
• Strong knowledge of statistical analysis tools and methodologies used in process validation.
• Experience with automation and control systems (PLCs, SCADA) validation is highly desirable.
• Familiarity with cleaning validation techniques, including swab/rinse sampling and analytical method parameters.
• Excellent technical writing skills with meticulous attention to detail and strong analytical, problem-solving, and root-cause analysis (RCA) capabilities.
• Effective communication and interpersonal skills, with the ability to lead cross-functional projects and mentor junior engineers and technicians.

Requirements:

• Work independently to identify, investigate, and resolve validation deviations and implement sustainable CAPA solutions.
• Serve as the site expert for the deployment, commissioning, qualification, and validation (CQV) of equipment and processes.
• Possess an analytical mindset to synthesize complex validation data and statistical analysis into compliant technical plans.
• Resolve difficult technical and compliance issues on compounding, filling, packaging, and automated lines.
• Manage multiple validation projects simultaneously in a fast-paced, dynamic manufacturing environment.

The functions of Sr. Engineer, Validation include, but are not limited by the following:

• Validation Strategy & Planning: Develop and execute the Master Validation Plan (MVP) for the facility. Define validation requirements for new equipment installations, automated systems, manufacturing processes, and utility systems (water, compressed air, HVAC).
• Protocol Development & Execution: Draft, review, and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols. Ensure all testing aligns with internal quality standards and external regulatory requirements.
• Process & Cleaning Validation: Design and oversee process validation studies and cleaning validation programs to prevent cross-contamination and guarantee consistent product quality.
• Risk Management & Deviation Resolution: Conduct risk assessments (e.g., FMEA) to identify critical control points. Lead investigations into validation deviations, author comprehensive deviation reports, and implement robust Corrective and Preventive Actions (CAPA).
• Cross-Functional Collaboration: Partner closely with Engineering, Production, Formulation, and Quality Assurance teams to ensure seamless technology transfers, equipment commissioning, and process improvements.
• Change Control & Re-validation: Manage the validation impact of engineering change controls. Evaluate modifications to equipment, systems, or processes and determine the necessary re-validation requirements to maintain a qualified state.
• Audit Readiness & Compliance: Maintain all validation documentation in an audit-ready state. Serve as a subject matter expert (SME) during internal audits, client audits, and regulatory inspections (FDA, OSHA, ISO).
• Mentorship & Continuous Improvement: Provide guidance, training, and mentorship to junior validation engineers and technicians. Stay updated on industry trends, advancing technologies, and regulatory updates to continuously optimize validation methodologies.

What's In It For You:

• Competitive Benefit Package (Medical, Dental, Vision, 401K, Pension Plan)
• Flexible Time Off (Paid Company Holidays, Paid Vacation, Vacation Buy Program, Volunteer Time, Summer Fridays & More!)
• Access to Company Perks (VIP Access to L'Oreal's Internal Shop for Discounted Products, Monthly Mobile Allowance)
• Learning & Development Opportunities (Unlimited Access to E-learnings, Lunch & Learn Sessions, Mentorship Programs, & More!)
• Employee Resource Groups (Think Tanks and Innovation Squads)
• Access to Mental Health & Wellness Programs

Don't meet every single requirement? At L'Oreal, we are dedicated to building a diverse, inclusive, and innovative workplace. If you're excited about this role but your past experience doesn't align perfectly with the qualifications listed in the job description, we encourage you to apply anyways! You may just be the right candidate for this or other roles!

We are an Equal Opportunity Employer and take pride in a diverse environment. We would love to find out more about you as a candidate and do not discriminate in recruitment, hiring, training, promotion, or other employment practices for reasons of race, color, religion, gender, sexual orientation, national origin, age, marital or veteran status, medical condition or disability, or any other legally protected status.