1

Contract Quality Engineer Medical Device Jobs in Delaware

Quality Engineer - Medical Device

Newark, DE ยท On-site

$70K - $90K/yr

Quality Engineer - Medical Device Location: Delaware Largescale Medical Device client facing a remediation project here on site in Delaware. What is the project the contractor will be working on?

Senior Software Engineer, Medical Device

Newark, DE ยท On-site

$119K - $157K/yr

Design and develop high quality software. * Develop and maintain software under an Agile/Scrum ... Medical device experience is a plus. * Medical imaging/general image processing is a plus.

... EU Medical Device Regulation, ISO 14971 (Risk Management), GMP, and GDP. * Familiarity with root ... product quality. Experience: * Bachelor's degree in Engineering (Mechanical, Biomedical ...

Product Quality Engineer 2

Newark, DE ยท On-site

$78K - $122K/yr

... EU Medical Device Regulation, ISO 14971 (Risk Management), GMP, and GDP. * Familiarity with root ... product quality. Experience: * Bachelor's degree in Engineering (Mechanical, Biomedical ...

Experience * 2-5+ years of quality engineering experience in a regulated manufacturing environment , preferably medical device, pharmaceutical, or healthcare packaging . * Experience with molding or ...

Experience * 2-5+ years of quality engineering experience in a regulated manufacturing environment , preferably medical device, pharmaceutical, or healthcare packaging . * Experience with molding or ...

Product Quality Engineer will make a direct impact on patient safety and product excellence by ... 13485, EU Medical Device Regulation, ISO 14970, Risk Management, GMP, and GDP * Ability to ...

Product Quality Engineer 3

Newark, DE ยท On-site

$85K - $133K/yr

Product Quality Engineer will make a direct impact on patient safety and product excellence by ... 13485, EU Medical Device Regulation, ISO 14970, Risk Management, GMP, and GDP * Ability to ...

... Contract Research and Knowledge Process Outsourcing Organization (CRO) dedicated to driving ... and medical device companies worldwide. Founded in , the company is headquartered in South ...

Provide product quality engineering support for on-market medical devices. This role will be ... 13485, EU Medical Device Regulation, ISO 14970, Risk Management, GMP, and GDP. * Ability to ...

Provide product quality engineering support for on-market medical devices. This role will be ... 13485, EU Medical Device Regulation, ISO 14970, Risk Management, GMP, and GDP * Ability to ...

Product Quality Engineer 1

Newark, DE ยท On-site

$54K - $86K/yr

Provide product quality engineering support for on-market medical devices. This role will be ... 13485, EU Medical Device Regulation, ISO 14970, Risk Management, GMP, and GDP. * Ability to ...

Product Quality Engineer 2

Newark, DE ยท On-site

$78K - $122K/yr

Provide product quality engineering support for on-market medical devices. This role will be ... 13485, EU Medical Device Regulation, ISO 14970, Risk Management, GMP, and GDP * Ability to ...

Product Quality Engineer 1

Newark, DE ยท On-site

$54K - $86K/yr

Provide product quality engineering support for on-market medical devices. This role will be ... 13485, EU Medical Device Regulation, ISO 14970, Risk Management, GMP, and GDP * Ability to ...

Provide product quality engineering support for on-market medical devices. This role will be ... 13485, EU Medical Device Regulation, ISO 14970, Risk Management, GMP, and GDP * Ability to ...

next page

Showing results 1-20

Contract Quality Engineer Medical Device information

What is the difference between Contract Quality Engineer Medical Device vs Contract Quality Engineer Pharmaceutical?

AspectContract Quality Engineer Medical DeviceContract Quality Engineer Pharmaceutical
CertificationsISO 13485, FDA QSR, GMPICH Q7, GMP, FDA regulations
Work EnvironmentMedical device manufacturing, labs, compliance auditsPharmaceutical production, labs, quality assurance
Industry UsageMedical device companies, OEMs, suppliersPharmaceutical firms, biotech companies, contract manufacturers

Both roles focus on quality assurance and regulatory compliance but differ mainly in industry-specific standards and environments. Contract Quality Engineers Medical Device work primarily with ISO 13485 and FDA QSR standards in device manufacturing, while Contract Quality Engineers Pharmaceutical focus on GMP and ICH Q7 regulations in drug production. Understanding these differences helps candidates target the right industry and certifications for their career goals.

What does a contract quality engineer do in the medical device industry?

A Contract Quality Engineer in the medical device industry is responsible for ensuring that products meet regulatory and company quality standards during a specific project or timeframe. They typically work on a contract basis, focusing on tasks like process validation, risk management, root cause analysis, and compliance with standards such as ISO 13485 and FDA regulations. Their role often involves collaborating with engineering, production, and regulatory teams to troubleshoot quality issues and implement corrective actions. They play a key role in maintaining product safety and regulatory compliance throughout the manufacturing process.

What are the key skills and qualifications needed to thrive as a contract quality engineer in the medical device industry?

To thrive as a Contract Quality Engineer in the Medical Device field, you need expertise in quality assurance, regulatory compliance (such as ISO 13485 and FDA regulations), and a background in engineering or life sciences. Familiarity with tools like CAPA systems, risk management software, and proficiency in quality management systems (QMS) is typically required. Strong analytical thinking, attention to detail, and effective communication skills set top performers apart in this role. These skills are essential to ensure product safety, regulatory compliance, and the successful launch and maintenance of medical devices in a highly regulated environment.

How does a contract quality engineer in the medical device industry typically collaborate with cross-functional teams?

As a Contract Quality Engineer in the medical device sector, you will frequently work closely with cross-functional teams, including R&D, manufacturing, regulatory affairs, and supply chain. Your responsibilities often involve reviewing design documentation, participating in risk assessments, and ensuring production processes meet both internal quality standards and regulatory requirements. Effective communication is key, as you'll be responsible for conveying quality expectations, addressing non-conformities, and supporting project timelines. This collaborative environment provides valuable experience in coordinating with diverse professionals while upholding strict industry standards.

What are the most commonly searched types of Quality Engineer Medical Device jobs in Delaware?

The most popular types of Quality Engineer Medical Device jobs in Delaware are:

What are popular job titles related to Contract Quality Engineer Medical Device jobs in Delaware?

For Contract Quality Engineer Medical Device jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Contract Quality Engineer Medical Device jobs in Delaware look for?

The top searched job categories for Contract Quality Engineer Medical Device jobs in Delaware are:

What cities in Delaware are hiring for Contract Quality Engineer Medical Device jobs?

Cities in Delaware with the most Contract Quality Engineer Medical Device job openings:

Quality Engineer - Medical Device

IT MINDS L.L.C.

Newark, DE โ€ข On-site

$70K - $90K/yr

Contractor

Re-posted 28 days ago


Job description

Role: Quality Engineer – Medical Device

Location:  Delaware

Largescale Medical Device client facing a remediation project here on site in Delaware.

What is the project the contractor will be working on?

•              We are seeking experienced Quality and/or Manufacturing Engineers to support a large-scale production documentation and remediation initiative at our client’s Newark, Delaware manufacturing site. These professionals will play a critical role in strengthening risk management practices, supporting transfer to manufacturing activities, and driving process validation and equipment qualification efforts.

o             This engagement will begin with comprehensive documentation gap assessments across multiple production lines, followed by remediation and implementation activities to ensure manufacturing readiness and compliance.

-            

Quality Engineer (Remediation)

Documentation Gap Analysis

•              Perform detailed reviews of production line documentation, including:

o             Process documentation

o             Work instructions

o             Training records

o             Validation documentation

o             Specifications and technical drawings

•              Identify documentation gaps, inconsistencies, and compliance risks.

•              Partner cross-functionally with manufacturing, quality, and engineering teams to prioritize findings.

Remediation & Implementation

•              Develop and execute remediation plans following gap assessments.

•              Update and create SOPs, work instructions, and validation documentation as needed.

•              Support transfer-to-manufacturing activities through structured risk mitigation.

•              Ensure documentation aligns with regulatory and internal quality standards.

Risk Management & FMEA

•              Lead and/or support:

o             Process FMEAs

o             Risk assessments tied to manufacturing transfer

o             Risk mitigation planning and documentation

•              Apply strong risk management principles to process validation and equipment qualification activities.

Process Validation & Equipment Qualification

•              Support process validation activities including:

o             IQ/OQ/PQ execution

o             Equipment qualification documentation

o             Validation protocol review and approval

•              Ensure alignment between validation activities and risk management outputs.

Technical Review & Support

•              Review engineering drawings and specifications to confirm accuracy and alignment with production processes.

o             Ability to read and interpret drawings is required (drafting not required).

•              Support sampling plan assessments:

o             Evaluate sampling plans and statistical justifications

o             Determine appropriate sample sizes and rationale

•              Participate in production line startup and manufacturing support as needed.

Skills:

Required:

•              3–6+ years of experience in Quality Engineering (QE) and/or Manufacturing Engineering within Medical Devices

•              Strong experience leading or supporting:

o             Process FMEAs

o             Risk management initiatives

o             Process validation activities

•              Experience reviewing and remediating manufacturing documentation.

•              Working knowledge of equipment qualification (IQ/OQ/PQ).

•              Ability to interpret engineering drawings and technical specifications.

Desired:

•              Experience with instrumentation and electronics (strong plus for the Delaware site).

•              Experience assessing sampling plans and statistical justifications (preferred but not required).

•            

•              Exposure to:

o             Plastics manufacturing

o             Chemistry-based processes or test strip formulation

o             Experience supporting multi-site environments.

Best Regards,

 

Satya Satish J | Technical Recruiter | IT Minds LLC |