Top 12 Sr. validation engineer Jobs in Lexington, Ky

Sr. Validation Engineer
Kindeva Drug Delivery Careers —Lexington, KY
- Full-time
- 5 years
- Engineering
- Master's degree
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Sr. Manager, Validation Engineer
Kindeva Drug Delivery Careers —Lexington, KY
- Full-time
- Engineering
- Office
- 3 years
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Sr. Mechanical Engineer
Xerox —Lexington, KY
- $109,818 - $192,000 a year
- Full-time
- Engineering
- SharePoint
- In-person
Senior Systems Engineer - Special Operations Forces
Lockheed Martin Corporation —Lexington, KY
- Part-time
- Machine learning
- Senior level
- AI
- Paid jury duty
- Paid holidays
Senior Software Development Engineer
CVS Health —Frankfort, KY
- $83,430 - $222,480 a year
- Full-time
- Azure
- System design
- HIPAA
- Health insurance
- Dental insurance
Sr. Manager, Manufacturing Engineering
Kindeva Drug Delivery Careers —Lexington, KY
- Full-time
- Engineering
- 11+ years
- Mentoring
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Senior Engineering Manager
Kindeva Drug Delivery Careers —Lexington, KY
- Full-time
- Engineering
- 11+ years
- Mentoring
Senior Project Engineer I
Kindeva Drug Delivery Careers —Lexington, KY
- Full-time
- 5 years
- Analysis skills
- Conflict management
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Sr. Validation Engineer

Kindeva Drug Delivery Careers -
Lexington, KY

Quick Apply

Job Details

Full-time

Qualifications

Content creation for technical audiences
Pharmaceutical regulatory compliance
Technical writing experience within manufacturing
FDA 21 CFR Part 11
ICH guidelines
Production validation processes
Biomedical regulatory compliance
Cross-functional communication

Full Job Description

Our Work Matters
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
As a Validation Engineer, you will play a critical role in ensuring our pharmaceutical manufacturing systems and processes meet rigorous regulatory and quality standards. You will lead and execute validation activities—including equipment, utilities, facilities, and process validations—to ensure our operations remain compliant and inspection-ready. Your expertise in cGMP, risk-based validation, and technical writing will directly impact the safety, efficacy, and consistency of the drug products we deliver. This is a highly visible, hands-on role ideal for a detail-oriented professional passionate about quality and continuous improvement in a dynamic, fast-paced environment

Responsibilities:
Validation Strategy & Execution

Develop, execute, and maintain validation protocols and reports (IQ, OQ, PQ) for equipment, utilities, and manufacturing processes.
Support commissioning and qualification (C&Q) activities for new equipment and facilities, ensuring compliance with FDA, EU, and global regulatory expectations.
Author and review validation lifecycle documentation, including plans, protocols, deviations, and final reports.
Partner with Engineering, Manufacturing, Quality, and Regulatory Affairs to ensure effective cross-functional validation planning and execution.
Perform periodic reviews and revalidation activities in accordance with lifecycle requirements.

Compliance & Risk Management

Lead risk assessments (FMEA, gap assessments) to determine validation strategy and appropriate testing requirements.
Provide validation input during change control, deviation investigations, and CAPA execution.
Ensure data integrity and good documentation practices in all validation records.
Act as subject matter expert (SME) during internal and external audits and inspections.

Continuous Improvement

Evaluate validation program effectiveness and recommend process improvements to enhance compliance, efficiency, and scalability.
Stay current with industry best practices and evolving regulatory guidance to ensure validation activities remain aligned with expectations.

Qualifications:

Bachelor’s degree in engineering, life sciences, or a related technical field.
5 or more years of validation experience; or 3 years with a Master’s degree

in a regulated pharmaceutical, biotech, or medical device environment.

Demonstrated knowledge of FDA, EU, and ICH regulatory requirements including 21 CFR Part 11 and Annex 15.
Experience in developing and executing validation documentation (IQ/OQ/PQ, protocols, reports).
Strong organizational, communication, and technical writing skills.
Ability to collaborate cross-functionally and manage multiple priorities in a deadline-driven environment.

Preferred Qualifications:

Familiarity with validation of automated systems and computerized system validation (CSV).
Experience with nasal or respiratory drug delivery systems, aseptic manufacturing, or cleanroom validation.
Working knowledge of validation tools and systems (e.g., TrackWise, ValGenesis, Veeva).
Lean Six Sigma or other continuous improvement training/certifications.

#LI-Onsite

California residents should review our Notice for California Employees and Applicants before applying.

Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees—regardless of format—without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.

Equal Opportunity Employer:
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.

Do you see yourself as part of the Kindeva mission? Click Apply Now Today!

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sr. validation engineer jobs in lexington, ky

Sr. Validation Engineer

Sr. Manager, Validation Engineer

Sr. Mechanical Engineer

Senior Systems Engineer - Special Operations Forces

Senior Software Development Engineer

Sr. Manager, Manufacturing Engineering

Senior Engineering Manager

Senior Project Engineer I

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