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Medical Design Jobs in Delaware (NOW HIRING)

Lead Design Assurance Engineer

Newark, DE · On-site

$119K - $186K/yr

In-depth understanding of medical device regulations and standards, including ISO 13485, ISO 14971, IEC 62366, IEC 60601, 21 CFR Part 820, MDD 93/42/EEC, EU MDR, and MDSAP. * Familiarity with ...

Lead Design Assurance Engineer

Newark, DE · On-site

$119K - $186K/yr

In-depth understanding of medical device regulations and standards, including ISO 13485, ISO 14971, IEC 62366, IEC 60601, 21 CFR Part 820, MDD 93/42/EEC, EU MDR, and MDSAP. * Familiarity with ...

Expertise in FDA Quality System Regulations, especially Design Control requirements, ISO 13485, and Medical Device Directive. * Familiarity with ISO 14970, IEC 60601, IEC 62366, and EN 62304.

Take Your Design Career to the Next Level Kleinfelder, a Forbes' Top Employer for Engineers in ... including: medical, dental, vision, life insurance, 401(k) plan, and paid holidays. * Career ...

Take Your Design Career to the Next Level Kleinfelder, a Forbes' Top Employer for Engineers in ... including: medical, dental, vision, life insurance, 401(k) plan, and paid holidays. Career ...

Take Your Design Career to the Next Level Kleinfelder, a Forbes' Top Employer for Engineers in ... including: medical, dental, vision, life insurance, 401(k) plan, and paid holidays. Career ...

Take Your Design Career to the Next Level Kleinfelder, a Forbes' Top Employer for Engineers in ... including: medical, dental, vision, life insurance, 401(k) plan, and paid holidays. Career ...

Take Your Design Career to the Next Level Kleinfelder, a Forbes' Top Employer for Engineers in ... including: medical, dental, vision, life insurance, 401(k) plan, and paid holidays. Career ...

Take Your Design Career to the Next Level Kleinfelder, a Forbes' Top Employer for Engineers in ... including: medical, dental, vision, life insurance, 401(k) plan, and paid holidays. Career ...

CAD Designer

Newark, DE · On-site

$26.50 - $36.50/hr

The CAD Designer will play a key role in supporting the engineering and design teams by producing ... Comprehensive Health Coverage - including Medical, Dental, Vision, plus Health Savings and Flexible ...

CAD Technician

Milford, DE · On-site

$20 - $32/hr

Our CAD Technicians help to enhance, maintain, and protect the communities we work, live, and play ... Medical, dental and vision insurance * Life and disability insurance * 401(k) plan with company ...

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Medical Design information

What is medical design?

Medical design refers to the process of creating and developing medical devices, equipment, and solutions that improve patient care and healthcare outcomes. Professionals in this field use engineering, biology, and design principles to ensure that medical products are safe, effective, and user-friendly. Medical design can involve anything from surgical tools to diagnostic machines and wearable health technologies. The process typically includes research, concept development, prototyping, testing, and regulatory approval. Collaboration with healthcare professionals and understanding patient needs are essential aspects of medical design.

What are the key skills and qualifications needed to thrive in medical design, and why are they important?

To thrive in Medical Design, you need a strong background in biomedical engineering or industrial design, combined with knowledge of anatomy, materials science, and regulatory standards. Familiarity with CAD software, rapid prototyping tools, and medical device regulations such as FDA or ISO standards is typically required. Creativity, attention to detail, and strong collaboration skills help professionals innovate while ensuring patient safety and usability. These skills are crucial for developing safe, effective, and user-friendly medical products that meet both clinical needs and compliance requirements.

What are some common challenges faced by professionals in medical design, and how can they be addressed?

Professionals in medical design often encounter challenges such as balancing regulatory compliance with innovative design, ensuring user safety, and collaborating effectively with multidisciplinary teams. Navigating stringent FDA or CE requirements while maintaining creativity can be demanding, but staying updated on regulations and involving regulatory experts early in the process helps. Close collaboration with clinicians, engineers, and end-users is crucial to create practical and user-friendly solutions. Frequent prototyping and user testing also help address usability issues before product launch.

What is the difference between Medical Design vs Medical Device Engineering?

AspectMedical DesignMedical Device Engineering
Required CredentialsDesign certifications, CAD skills, knowledge of medical regulationsEngineering degrees, technical certifications, regulatory knowledge
Work EnvironmentDesign studios, R&D labs, collaborative teamsEngineering labs, manufacturing facilities, technical teams
Employer & Industry UsageMedical device companies, healthcare product firmsMedical device manufacturers, biotech firms
Common Search & ComparisonOften compared for roles in product development and innovationFocuses more on technical engineering aspects

Medical Design primarily involves creating the conceptual and aesthetic aspects of medical products, focusing on user experience and compliance. Medical Device Engineering emphasizes the technical development, testing, and manufacturing of medical devices. Both roles are essential in bringing medical products to market but differ in their focus and skill sets.

How to get into medical design?

To enter medical design, candidates typically need a background in biomedical engineering, industrial design, or related fields, along with knowledge of medical device regulations and standards. Gaining experience through internships, certifications such as ISO 13485, and proficiency with CAD software can improve job prospects. Strong understanding of human factors and collaboration with healthcare professionals are also valuable in this field.

What does a medical designer do?

A medical designer develops and improves medical devices, equipment, and healthcare products by applying principles of engineering, design, and human factors. They often use CAD software and collaborate with healthcare professionals to ensure safety, functionality, and compliance with industry standards. Their work supports the creation of innovative solutions for patient care and medical procedures.

What are popular job titles related to Medical Design jobs in Delaware?

For Medical Design jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Medical Design jobs in Delaware look for?

The top searched job categories for Medical Design jobs in Delaware are:

What cities in Delaware are hiring for Medical Design jobs?

Cities in Delaware with the most Medical Design job openings:

Lead Design Assurance Engineer

Newark, DE • On-site

Hologic Inc.
Health Care and Social Assistance • 5 - 10K employees

$119K - $186K/yr

Full-time

Re-posted 17 days ago


Hologic rating

8.0

Company rating: 8.0 out of 10

Based on 25 frontline employees who took The Breakroom Quiz


Job description

Are you passionate about driving innovation while ensuring compliance and quality in medical device development? At Hologic, we are seeking a Lead Design Assurance Engineer to play a pivotal role in new product development, ensuring that design controls, risk management, and global regulatory compliance are maintained from concept to product launch. In this role, you'll work cross-functionally to define clear design requirements, oversee verification and validation processes, and champion continuous improvement initiatives. If you're a strategic thinker with hands-on expertise in design assurance and a commitment to delivering safe, reliable, and durable medical devices, we want to hear from you!

Knowledge:

  • In-depth understanding of medical device regulations and standards, including ISO 13485, ISO 14971, IEC 62366, IEC 60601, 21 CFR Part 820, MDD 93/42/EEC, EU MDR, and MDSAP.
  • Familiarity with reliability modeling and testing for electro-mechanical devices and capital equipment.
  • Expertise in design inputs/requirements analysis, design verification/validation, and design transfer processes.
  • Advanced knowledge of risk management principles, including hazard analysis and FMEA (Design, Usability, and Process).
  • Thorough understanding of test method validation, statistical methods, and failure investigations/root cause analysis.

Skills:

  • Proven ability to lead design assurance efforts across the product lifecycle, from concept to launch and post-market activities.
  • Strong analytical and problem-solving skills to identify gaps, assess risk, and implement corrective actions.
  • Effective project management skills, including prioritization, planning, and timely execution of critical tasks.
  • Exceptional communication and collaboration skills to work with cross-functional teams and ensure alignment on design and compliance goals.
  • Ability to critically assess and advocate for compliance in written product and project documentation.
  • Leadership and mentoring skills to guide junior engineers and foster a culture of quality and innovation.
  • Familiarity with continuous improvement practices and strategies to optimize processes and enhance product quality.

Behaviors:

  • Ownership-driven, taking responsibility for deliverables and ensuring adherence to regulatory and quality standards.
  • Proactive and detail-oriented, with a focus on driving efficiency and maintaining compliance.
  • Collaborative and team-oriented, building strong relationships across R&D, Regulatory Affairs, Manufacturing, and other key stakeholders.
  • Customer-focused, committed to developing innovative solutions that enhance product safety, reliability, and usability.
  • Strategic thinker, leveraging data and industry insights to inform decisions and improve processes.
  • Committed to continuous improvement, driving initiatives to optimize product development and design assurance performance.

Experience:

  • Bachelor of Science degree in a related engineering discipline required; Master's degree preferred.
  • 8+ years of medical device industry experience with a Bachelor's degree in a related engineering discipline, or 5+ years of experience with a Master's degree.
  • Hands-on experience with electro-mechanical devices and capital equipment is preferred.
  • Proven track record in design assurance activities, including verification/validation, risk management, and regulatory compliance.
  • Demonstrated expertise in test method validation, statistical analysis, and root cause failure investigations.

Why join Hologic?
We are committed to making Hologic the destination for top talent. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career.
The annualized base salary range for this role is $119,300 - $186,600 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, education, business needs and market demand.
Agency and Third-Party Recruiter Notice
Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.
Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.

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