Top 399 Validation engineering lead Jobs in Springfield, 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
Radar Systems Engineer
Thunderbolt Logistics —Moorestown, NJ
- $85,000 - $130,000 a year
- Full-time
- Computer Science
- Engineering
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Entry Level Process/Industrial Engineer
PMI (Penn Manufacturing Industries) —Montgomeryville, PA
- From $50,000 a year
- Full-time
- AutoCAD
- Management
- Supervising experience
Quick Apply
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
9d
Global Automation Engineering & Technology Head
CSL Behring —King of Prussia, PA
- Full-time
- Computer science
- Computer Science
- 5 years
Senior Quality Assurance Automation Manager
United States Cold Storage Inc —Camden, NJ
- $160,000 - $190,000 a year
- Hybrid work
- Azure
- Computer Science
- 5 years
- Commuter assistance
- AD&D insurance
Quick Apply
Quality Manager
Omega Engineering Inc —Swedesboro, NJ
- Full-time
- Microsoft Outlook
- Mid-level
- Office
Quick Apply
Process Engineer II
Polysciences, Inc. —Warrington, PA
- $100,000 - $125,000 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Engineering
- Paid parental leave
- Paid holidays
Quick Apply
Quality Manager
Dwyer Instruments Inc —Philadelphia, PA
- $90,000 - $120,000 a year
- Full-time
- Microsoft Outlook
- Mid-level
- Ability to lift 50 pounds
Manufacturing Manager
GWYNEDD —North Wales, PA
- $85,000 - $100,000 a year
- 8 hour shift
- Engineering
- Mid-level
- 3 years
Quick Apply
8d
Manager, Product Validation & Product Transfer
Hikma Pharmaceuticals PLC —Cherry Hill, NJ
- $92,850 - $158,450 a year
- Full-time
- Microsoft Excel
- Bachelor of Science
- Quality control
- Paid parental leave
- Paid holidays
Quick Apply
New Product Launch Specialist
Accupac —Mainland, PA
- $80,000 - $90,000 a year
- Online Application
- Hybrid work
- 5 years
- Mid-level
- Analysis skills
- Health savings account
- Paid holidays
Quick Apply
Quality Manager
Dwyer Instruments Inc —Swedesboro, NJ
- $90,000 a year
- Full-time
- Microsoft Outlook
- Mid-level
- Office
Quality Manager
Omega Engineering Inc —Swedesboro, NJ
- $90,000 - $120,000 a year
- Full-time
- Microsoft Outlook
- Mid-level
- Office
Quick Apply
Principal Electronics Engineer (RELOCATION ASSIST)
Leoforce —Andalusia, PA
- $140,000 - $160,000 a year
- Senior level
- Mechanical knowledge
Quick Apply
12d
Senior HCM Business Analyst
CAI —New Castle, DE
- $62 - $67 an hour
- Full-time
- 7 years
- Office
- Analysis skills
- Health insurance
- Dental insurance
3d
Validation Engineering Roles
Design Group —Philadelphia, PA
- Full-time
- Background check
- Engineering
- Pass drug screening
EMS Validation Engineering Lead
Schneider Electric —Horsham, PA
- Online Application
- Up to 50% travel
- System design
- Business development
- Wellness program
- Health insurance
Validation Engineer
GlaxoSmithKline —King of Prussia, PA
- Full-time
- Mid-level
- Organizational skills
- 1 year
8d
Validation - Lead Engineer - Project Farma
PerkinElmer —Upper Providence, PA
- $95,000 - $110,000 a year
- Full-time
- Military
- Data analysis skills
- Analysis skills
6d

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validation engineering lead jobs near springfield, 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 engineering lead jobs in springfield, pa

Quality Engineer

Radar Systems Engineer

Entry Level Process/Industrial Engineer

Senior Substation Engineer

Global Automation Engineering & Technology Head

Senior Quality Assurance Automation Manager

Quality Manager

Process Engineer II

Quality Manager

Manufacturing Manager

Manager, Product Validation & Product Transfer

New Product Launch Specialist

Quality Manager

Quality Manager

Principal Electronics Engineer (RELOCATION ASSIST)

Senior HCM Business Analyst

Validation Engineering Roles

EMS Validation Engineering Lead

Validation Engineer

Validation - Lead Engineer - Project Farma

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