Top 72279 Fast Engineer Jobs

Quality Engineer
Drummond Scientific Company —Broomall, PA
- $82,000 a year
- Full-time
- Background check
- Engineering
- Analysis skills
- Health insurance
- Dental insurance
Quick Apply
Mechanical Quality Engineer
Marsh Bellofram —New Cumberland, WV
- Full-time
- Background check
- Engineering
- Mid-level
- Health insurance
- Dental insurance
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Power Electronics Engineer
Analogic Corporation —Canton, MA
- Data analysis skills
- Mid-level
- 3 years
- Health savings account
- Disability insurance
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Systems Engineer (Mid-Level)
Relative Dynamics —Sioux Falls, SD
- Full-time
- Background check
- Mid-level
- In-person
- Paid holidays
- Disability insurance
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Process Engineer
Alsip MiniMill, LLC —Alsip, IL
- $145,000 - $165,000 a year
- Engineering
- Mid-level
- Analysis skills
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MECHANICAL DESIGNER/ENGINEER - FROM FRESH GRAD TO FULL LOAD
Nelson-Rudie & Associates, Inc. —Overland Park, KS
- $60,000 - $150,000 a year
- Full-time
- Remote
- Office
- Mentoring
- Associate's degree
- Health insurance
- Dental insurance
Quick Apply
14d
Full Stack Software Engineer
Confidential Posting —San Francisco, CA
- $130,000 - $180,000 a year
- Weekends as needed
- Computer Science
- Mid-level
- Master's degree
- Health insurance
- Dental insurance
Quick Apply
Server Side Java Engineer with Twitter API Experience
Sonsoft Inc —Sunnyvale, CA
- Contract
- 5 years
- US work authorization
- Senior level
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Server Side Java Engineer with Twitter API Experience
Sonsoft Inc —Sunnyvale, CA
- Contract
- 5 years
- US work authorization
- Senior level
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Firmware Engineer
Manpower Engineering —Saint Paul, MN
- Full-time
- Maintenance
- Mid-level
- Electrical Engineering
- Health savings account
- Disability insurance
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Sr Systems Engineer
Manpower Engineering —Phoenix, AZ
- $101 an hour
- Computer science
- Computer Science
- CAD
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IT Application Engineer
Manpower Engineering —Foster City, CA
- $83 an hour
- Computer science
- Computer Science
- Mid-level
- Health savings account
- Disability insurance
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Manufacturing Engineer
Experis —Saint Paul, MN
- $45 an hour
- Contract
- Mid-level
- Analysis skills
- In-person
- Health savings account
- Disability insurance
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8d
Software Engineer - Secure Code Analysis & Modernization (Senior and Junior roles available)
Canvass Labs —Remote
- $120,000 - $220,000 a year
- Full-time
- Remote
- Databases
- Analysis skills
- US work authorization
- Health insurance
- 401(k)
Quick Apply
13d
ENG Design Engineer I
Experis —Maplewood, MN
- Contract
- Analysis skills
- Communication skills
- Entry level
- Health savings account
- Disability insurance
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7d
End to End Systems Engineer
Manpower Engineering —Foster City, CA
- $80 - $85 an hour
- Computer science
- Computer Science
- 5 years
- Health savings account
- Disability insurance
Quick Apply
IT Application Engineer
Manpower Engineering —Foster City, CA
- $75 - $80 an hour
- 6 years
- Computer Science
- Office
- Health savings account
- Disability insurance
Quick Apply
Hardware Software Integration Engineer
Manpower Engineering —Foster City, CA
- $74 an hour
- Computer Science
- Mid-level
- Master's degree
- Health savings account
- Disability insurance
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Software Engineer
Manpower Engineering —Foster City, CA
- $100 - $105 an hour
- 7 years
- Computer Science
- Bachelor of Science
- Health savings account
- Disability insurance
Quick Apply
Quality Engineer
Entegee —Raynham, MA
- $45 - $55 an hour
- Contract
- Bachelor of Science
- Mid-level
- Bachelor's degree
- Commuter assistance
- Disability insurance
Quick Apply

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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

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