Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Engineering
Validation Engineer
Swiftwater, PA

Find & Apply For Validation Engineer Jobs in Swiftwater, Pennsylvania

Browse jobs from a variety of sources below, sorted with the most recently published, nearest to the top. Click the title to view more information and apply online.

Skip to job details
Now viewing: Quality Validation Engineer
Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

Katalyst Healthcares & Life Sciences

Quality Validation Engineer

Pay: Not specified
Posted: 2 weeks ago
Location: 2 locations (Onsite)
Last Updated: 2 weeks ago
Hours: Full-Time
Expires: 10/19/2026

Choose a Location

This role is available in multiple locations. Pick one to apply.

Review key factors to help you decide if the role fits your goals.
How is this calculated?
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
65
out of 100
Average of individual scores

Were these scores useful?

Job Description

Qualifications & Experience:
Bachelor's degree in Engineering, Life Sciences, or a related technical discipline required; Master's degree preferred. 6-9 years of experience in the pharmaceutical, biopharmaceutical, or other highly regulated manufacturing environments. Strong background in quality validation, quality systems, and regulatory compliance within the life sciences industry. Demonstrated experience leading and managing Corrective and Preventive Action (CAPA) investigations and activities. Comprehensive knowledge of Quality System Regulations (QSR), GxP requirements, and industry best practices. Experience supporting validation activities, including equipment, process, facility, computerized systems, and documentation review. Preferred experience in high-speed aseptic filling operations and sterile manufacturing environments. Proven ability to collaborate effectively with cross-functional teams, including Quality, Manufacturing, Engineering, Validation, and Regulatory Affairs. Strong analytical and problem-solving skills with exceptional attention to detail. Ability to manage multiple projects simultaneously while meeting aggressive timelines and strict deadlines. Excellent verbal and written communication skills, with the ability to present complex information clearly to diverse stakeholders. Self-motivated, organized, and capable of working independently in a fast-paced, regulated environment.
Key Competencies:
Quality Validation & Compliance. CAPA Management. Regulatory Knowledge (FDA, GMP, GxP, QSR). Risk Assessment & Root Cause Analysis. Cross-Functional Collaboration. Project Management. Technical Documentation & Reporting. Continuous Improvement & Quality Excellence.
Skills need:
10+ years of experience in a Quality/Validation role. Strong background in quality validation, quality systems, and regulatory. compliance within the life sciences industry. Extensive CAPA experience. Extensive Quality Systems Experience. Extensive experience in high-speed aseptic filling operations and sterile manufacturing environments.