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Medical Design Jobs in California (NOW HIRING)

Sr Program Manager, R&D

San Diego, CA · On-site

$123K - $123K/yr

... and medical design and development cycles. Preferred : • MS, M.B.A or equivalent degree preferred. • PMP Certification preferred. • Experience within Diagnostics marketplace preferred;

Sr Program Manager, R&D

San Diego, CA · On-site

$147K - $245K/yr

Experience with ISO and FDA quality systems regulations and medical design and development cycles The annualized base salary range for this role is $147,000 to $245,000 and is bonus eligible. Final ...

... design transformational technologies. Whether it's harnessing fusion through the science of stars, making exponential leaps in power efficiency, or innovating medical care with a novel cancer ...

Experience with ISO and FDA quality systems regulations and medical design and development cycles The annualized base salary range for this role is $147,000 to $245,000 and is bonus eligible. Final ...

Experience with Medical Design Control processes. * Experience with Bug Tracking tools. * Experience with Requirements Management Tools. * Experience with Test Management Tools. Additional ...

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Showing results 1-20

Medical Design information

See California salary details

$22.5K

$80.8K

$124.9K

How much do medical design jobs pay per year?

As of Aug 7, 2026, the average yearly pay for medical design in California is $80,777.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,596.00 and $105,756.00 per year, depending on experience, location, and employer.

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 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 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.

What cities in California are hiring for Medical Design jobs? Cities in California with the most Medical Design job openings:
Infographic showing various Medical Design job openings in California as of August 2026, with employment types broken down into 72% Full Time, and 28% Part Time. Highlights an 100% In-person job distribution, with an average salary of $80,777 per year, or $38.8 per hour.

Sr Program Manager, R&D

Hologic, Inc.

San Diego, CA • On-site

$123K - $123K/yr

Full-time

Re-posted 18 days ago


Hologic rating

8.0

Company rating: 8.0 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

174th of 487 rated machine equipment manufacturers


Job description

Job Summary:
Hologic, Inc. is a leading medical technology company dedicated to advancing women’s health and well-being. They are seeking a Sr Program Manager for their Diagnostics division who will manage new assay development and engineering projects, leading cross-functional teams to ensure successful project delivery.
Responsibilities:
• Act as an independent leader of complex instrument systems and platforms programs, technically challenging product development projects, and diverse product sustaining initiatives involving cross-functional teams.
• Establish project objectives and work plans including schedule, budgets, and resource requirements.
• Delegate assignments to functional area team members and track key project activities to successful completion. Report project status to divisional leadership.
• Lead, coach, guide, and mentor a team of highly motivated, high performing PMO team members.
• Responsible for the management of large international, cross-functional, business critical programs
• Exert influence within a highly matrixed organization
• Apply expertise to influence the future strategy of the PMO function and implement best practices
• Utilize expertise to proactively identify and resolve product and project risks
• Drive for program success while ensuring consistency and alignment across all product development projects by overcoming constraints, problems, and issues
• Exceed customer expectations, while maximizing value to Hologic and maintaining GMP FDA/ISO compliance
Qualifications:
Required:
• BS Degree in Science or Engineering required.
• Minimum of 8 - 10 years’ experience in Program Management leading large, cross functional development programs, with demonstrated experience leading diverse sustainability projects such as product improvements, reliability, regulatory, custom, regional, product lifecycle, and others.
• Expert in Program Management/Leadership.
• Advanced knowledge and deep understanding of stage-gate Product Development process.
• Expert in Product Development including Design Control procedures.
• Expert in management of project risks.
• Expert communication and interpersonal skills.
• Advanced talent management and development skills.
• Experience with ISO and FDA quality systems regulations and medical design and development cycles.
Preferred:
• MS, M.B.A or equivalent degree preferred.
• PMP Certification preferred.
• Experience within Diagnostics marketplace preferred; Molecular Diagnostics experience is a plus.
Company:
We’re an innovative medical technology company whose purpose is to enable healthier lives everywhere, every day. Founded in 1985, the company is headquartered in Marlborough, USA, with a team of 5001-10000 employees. The company is currently Late Stage.

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