Top 307 Validation engineer Jobs in West Chester Pa

Quality Engineer
Drummond Scientific Company —Broomall, PA
- $82,000 a year
- Full-time
- Background check
- Engineering
- Analysis skills
- Health insurance
- Dental insurance
Quick Apply
Validation / Verification Eng, Engineer
Synopsys —Exton, PA
- $76,000 - $114,000 a year
- Computer Science
- Software troubleshooting
- Mid-level
1d
Validation Engineer
GlaxoSmithKline —King of Prussia, PA
- Full-time
- Mid-level
- Organizational skills
- 1 year
8d
GxP Validation Engineer
Prana Life Sciences Llc —Exton, PA
- Email
- HIPAA
- Mid-level
- Bachelor's degree
- Health insurance
- 401(k)
Validation - Engineer I / II - Project Farma
PerkinElmer —Upper Providence, PA
- Full-time
- Customer service
- Military
- Data analysis skills
Validation/Verification Engineer - Computer Science Focus (Exton, PA) - 13924
Synopsys —Exton, PA
- $76,000 - $114,000 a year
- Computer Science
- Software troubleshooting
- Windows
6420 - Senior CSV Engineer / Senior Validation Engineer
Verista, Inc. —King of Prussia, PA
- $70,491 - $118,062 a year
- Remote
- Senior level
- SDLC
- Commuter assistance
- Paid parental leave
Quick Apply
10d
Validation Engineer
CAI —King of Prussia, PA
- $72,800 - $80,100 a year
- Full-time
- Customer service
- Mid-level
- Team management
- Disability insurance
- Health insurance
Quick Apply
Senior Validation Engineer
GlaxoSmithKline —King of Prussia, PA
- Full-time
- Management
- Computer Science
- 5 years
3d
Quality Control Manager
ACTION MANUFACTURING COMPANY —Atglen, PA
- Full-time
- Background check
- 6 years
- Computer Science
Quick Apply
Electrical Engineer - RF Systems
Asylon —Norristown, PA
- $115,000 - $150,000 a year
- Full-time
- Schematics
- Mid-level
- 3 years
- Relocation assistance
- Health insurance
Quick Apply
8d
Senior Substation Engineer
SEL Engineering Services, Inc. —King of Prussia, PA
- $136,100 - $170,300 a year
- Full-time
- Management
- Bachelor of Science
- System design
- Paid holidays
- Disability insurance
Quick Apply
10d
Senior System Engineer
CACI —King of Prussia, PA
- $90,300 - $189,600 a year
- Full-time
- Computer Science
- 5 years
- Machine learning
- Health insurance
Principal Engineer – Beta Star
R-V Industries, Inc. —Honey Brook, PA
- Full-time
- Customer service
- 5 years
- Bachelor of Science
- Health savings account
- Health insurance
Quick Apply
Software Build & Release Engineer
Noblis —Philadelphia, PA
- $78,900 - $123,300 a year
- Full-time
- Computer Science
- System design
- 3 years
- Health insurance
- Tuition reimbursement
Project Design Engineer
GWYNEDD MANUFACTURING INC —North Wales, PA
- $70,000 - $100,000 a year
- 8 hour shift
- Organizational skills
- Senior level
- Communication skills
Quick Apply
Packaging Engineer
Entegee —Fort Washington, PA
- $55 - $63 an hour
- Contract
- Bachelor of Science
- Mid-level
- Bachelor's degree
- Commuter assistance
- Disability insurance
Quick Apply
4d
Senior System Test & Validation Engineer
Waters Corporation —New Castle, DE
- $92,000 - $153,000 a year
- Azure
- 5 years
- DevOps
Validation / Verification Eng, Sr Engineer
Synopsys —Exton, PA
- $91,000 - $137,000 a year
- Computer Science
- Windows
- Master's degree
1d
Process Engineer
AMETEK, Inc. —Exton, PA
- $80,000 - $100,000 a year
- Pass drug screening
- Mid-level
- Electrical Engineering
- AD&D insurance
- Paid holidays

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validation engineer jobs near west chester pa

Quality Engineer

Drummond Scientific Company -
Broomall, PA

Quick Apply

Job Details

Full-time
$82,000 a year

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Parental leave
Employee assistance program
Vision insurance
401(k) matching
Life insurance
Retirement plan

Qualifications

Statistics
Defect resolution root cause analysis
Preventive action implementation
Engineering
Statistical Process Control
Corrective and preventive actions (CAPA)
GMP
ASQC Certification
Bachelor's degree in engineering
Bachelor's degree
Medical device manufacturing facility experience
Attention to detail
Process validation (IQ/OQ/PQ)
Biomedical regulatory compliance
Root cause analysis
PPAP
Process management
ISO 13485
FDA regulations
Customer complaint resolution
Failure analysis

Full Job Description

*Applicants must be authorized to work in the U.S. without current or future visa sponsorship.

*This role is fully on-site and based in Broomall, PA. We are unable to offer relocation assistance for this role.

Company:

Drummond Scientific Company, located just outside of Philadelphia, PA, is a family-owned company that leverages nearly 75 years of experience to maintain its position as an elite developer and manufacturer of consumable medical devices, which includes both microvolume liquid transfer technology and rapid diagnostics. Our branded products can be found in laboratories across the globe and are continuously recognized for their durability and reliability. Despite the notoriety gained from the products bearing the Drummond name, what truly establishes the company as an industry leader is its role as a contract manufacturer. Parts made by Drummond have helped create and save lives by revolutionizing the field of in vitro fertilization and enabling the diagnostic technologies of many of the largest, and most innovative, companies in the world.

Scope of Position

The Quality Engineer ensures that all medical devices are designed, manufactured, and distributed in compliance with FDA 21 CFR Part 820, ISO 13485, and other applicable regulatory and customer requirements. This role drives product quality, process capability, and continuous improvement across the manufacturing lifecycle, supporting both new product development and ongoing production.

Key Responsibilities

Maintain and improve the Quality Management System (QMS) in alignment with ISO 13485, FDA QSR, and internal procedures.
Lead and support internal audits, supplier audits, and regulatory inspections.
Own and manage quality system elements such as CAPA, NCRs, complaint handling, and document control.
Develop, validate, and monitor manufacturing processes using statistical tools (SPC, DOE, MSA).
Support production teams in resolving quality issues, identifying root causes, and implementing corrective and preventive actions.
Create and maintain inspection plans, sampling plans, and quality control documentation.
Participate in design reviews, ensuring compliance with Design Control requirements.
Support verification and validation (V&V) activities, including test method validation.
Evaluate and qualify suppliers; maintain supplier performance metrics.
Review and approve supplier PPAPs, first article inspections, and material certifications.
Drive supplier corrective actions and continuous improvement initiatives.
Analyze quality data to identify trends, process capability, and improvement opportunities.
Prepare quality reports for management, including KPIs, audit findings, and CAPA status.
Use statistical software (e.g., Minitab) to support data-driven decision-making.

Qualifications

Bachelor’s degree in engineering (Mechanical, Biomedical, Industrial, or related field).
2–5 years of experience in a regulated manufacturing environment; medical device experience strongly preferred.
Working knowledge of ISO 13485, 21 CFR Part 820, ISO 14971, and GMP.
Experience with CAPA, root cause analysis tools (5 Whys, Fishbone), and process validation (IQ/OQ/PQ).
Proficiency with statistical analysis and quality tools (SPC, MSA, DOE).
ASQ certifications (CQE, CQA) are a plus.

Desired Skills & Abilities

Strong analytical and problem‑solving skills.
Ability to interpret engineering drawings and specifications.
Excellent communication and cross‑functional collaboration.
Detail‑oriented mindset with a commitment to product safety and compliance.
Ability to manage multiple priorities in a fast‑paced environment.

Travel Requirements

Travel will be <5%

Employment Type

Full-time

Pay: $82,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Employee assistance program
Health insurance
Life insurance
Paid time off
Parental leave
Retirement plan
Vision insurance

Application Question(s):

Will you now, or in the future, require sponsorship for employment visa status (e.g. H-1B visa status)?

Experience:

medical device manufacturing: 3 years (Required)
ISO 13485, 21 CFR Part 820, ISO 14971, and GMP: 1 year (Required)

Ability to Commute:

Broomall, PA 19008 (Required)

Work Location: In person

Quick Apply

Refine Your Search

validation engineer jobs in west chester pa

Quality Engineer

Validation / Verification Eng, Engineer

Validation Engineer

GxP Validation Engineer

Validation - Engineer I / II - Project Farma

Validation/Verification Engineer - Computer Science Focus (Exton, PA) - 13924

6420 - Senior CSV Engineer / Senior Validation Engineer

Validation Engineer

Senior Validation Engineer

Quality Control Manager

Electrical Engineer - RF Systems

Senior Substation Engineer

Senior System Engineer

Principal Engineer – Beta Star

Software Build & Release Engineer

Project Design Engineer

Packaging Engineer

Senior System Test & Validation Engineer

Validation / Verification Eng, Sr Engineer

Process Engineer

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