Support EU MDR remediation projects for orthopedic medical device products. * Review, update, and maintain Design History Files (DHFs) and technical documentation. * Perform design assurance ...
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Support EU MDR remediation projects for orthopedic medical device products. * Review, update, and maintain Design History Files (DHFs) and technical documentation. * Perform design assurance ...
Regulatory Compliance and MDR * Ensure compliance with applicable medical device regulations including EU MDR 2017/745, FDA Quality System Regulation (as applicable), and other global regulatory ...
Regulatory Compliance and MDR * Ensure compliance with applicable medical device regulations including EU MDR 2017/745, FDA Quality System Regulation (as applicable), and other global regulatory ...
Regulatory Affairs Associate
Sylmar, CA · On-site
$40 - $45/hr
Exposure to authoring and/or supporting PMA supplements and familiarity with EU MDR (2017/745) requirements are desirable. * Working knowledge of FDA PMA guidance documents, 21 CFR regulations, and ...
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Regulatory Affairs Associate
Sylmar, CA · On-site
$40 - $45/hr
Exposure to authoring and/or supporting PMA supplements and familiarity with EU MDR (2017/745) requirements are desirable. * Working knowledge of FDA PMA guidance documents, 21 CFR regulations, and ...
Regulatory Compliance and MDR * Ensure compliance with applicable medical device regulations including EU MDR 2017/745, FDA Quality System Regulation (as applicable), and other global regulatory ...
Regulatory Compliance and MDR * Ensure compliance with applicable medical device regulations including EU MDR 2017/745, FDA Quality System Regulation (as applicable), and other global regulatory ...
Principal Engineer (Mechanical / Electro-mech
Lompoc, CA · On-site
$133K - $183K/yr
The role operates in a highly regulated medical device environment governed by 21 CFR 820, ISO 13485:2016, and EU MDR 2017/745. Core areas include providing technical ownership of the electro ...
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Principal Engineer (Mechanical / Electro-mech
Lompoc, CA · On-site
$133K - $183K/yr
The role operates in a highly regulated medical device environment governed by 21 CFR 820, ISO 13485:2016, and EU MDR 2017/745. Core areas include providing technical ownership of the electro ...
Senior Quality Engineer
Mountain View, CA · Hybrid
$180K - $200K/yr
Ensure compliance with design control requirements (ISO 13485, FDA 21 CFR Part 820, EU MDR, and Health Canada regulations) throughout the product lifecycle. * Partner with R&D and cross-functional ...
Senior Quality Engineer
Mountain View, CA · Hybrid
$180K - $200K/yr
Ensure compliance with design control requirements (ISO 13485, FDA 21 CFR Part 820, EU MDR, and Health Canada regulations) throughout the product lifecycle. * Partner with R&D and cross-functional ...
Regulatory Affairs Associate
Lake View Terrace, CA · On-site
$40 - $46/hr
PMA supplements (30-day Notices, Real-Time Reviews, 180-Day Supplements, Annual Reports), as well as supporting EU MDR Technical Documentation updates, change assessments, and Notified Body ...
Regulatory Affairs Associate
Lake View Terrace, CA · On-site
$40 - $46/hr
PMA supplements (30-day Notices, Real-Time Reviews, 180-Day Supplements, Annual Reports), as well as supporting EU MDR Technical Documentation updates, change assessments, and Notified Body ...
$40 - $46/hr
S PMA supplements (30-day Notices, Real-Time Reviews, 180-Day Supplements, Annual Reports), as well as supporting EU MDR Technical Documentation updates, change assessments, and Notified Body ...
$40 - $46/hr
S PMA supplements (30-day Notices, Real-Time Reviews, 180-Day Supplements, Annual Reports), as well as supporting EU MDR Technical Documentation updates, change assessments, and Notified Body ...
Maintenance Technician - Stella (MDR)
Marina Del Rey, CA · On-site
$20.75 - $25/hr
ABOUT GREYSTAR Greystar is a leading, fully integrated global real estate platform offering expertise in property management, investment management, development, and construction services in ...
Maintenance Technician - Stella (MDR)
Marina Del Rey, CA · On-site
$20.75 - $25/hr
ABOUT GREYSTAR Greystar is a leading, fully integrated global real estate platform offering expertise in property management, investment management, development, and construction services in ...
Regulatory Affairs and Quality Assurance Specialist
Huntington Beach, CA · On-site
$90K - $120K/yr
EU MDR * FDA QSR * ISO 13485 / MDSAP * Review and approve product labeling, including IFUs, packaging, and marketing materials * Ensure UDI compliance for U.S., EU, and other global jurisdictions
Regulatory Affairs and Quality Assurance Specialist
Huntington Beach, CA · On-site
$90K - $120K/yr
EU MDR * FDA QSR * ISO 13485 / MDSAP * Review and approve product labeling, including IFUs, packaging, and marketing materials * Ensure UDI compliance for U.S., EU, and other global jurisdictions
Senior Quality Engineer
Mountain View, CA · On-site
$180K - $200K/yr
Ensure compliance with design control requirements (ISO 13485, FDA 21 CFR Part 820, EU MDR, and Health Canada regulations) throughout the product lifecycle. * Partner with R&D and cross-functional ...
Senior Quality Engineer
Mountain View, CA · On-site
$180K - $200K/yr
Ensure compliance with design control requirements (ISO 13485, FDA 21 CFR Part 820, EU MDR, and Health Canada regulations) throughout the product lifecycle. * Partner with R&D and cross-functional ...
EU MDR * FDA QSR * ISO 13485 / MDSAP * Review and approve product labeling, including IFUs, packaging, and marketing materials * Ensure UDI compliance for U.S., EU, and other global jurisdictions
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EU MDR * FDA QSR * ISO 13485 / MDSAP * Review and approve product labeling, including IFUs, packaging, and marketing materials * Ensure UDI compliance for U.S., EU, and other global jurisdictions
NPI Buyer
Irvine, CA · On-site
Lead sourcing strategy for new product development, ensuring alignment with FDA 21 CFR 820, ISO 13485, and EU MDR supplier control requirements. * Negotiate complex development agreements, commercial ...
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NPI Buyer
Irvine, CA · On-site
Lead sourcing strategy for new product development, ensuring alignment with FDA 21 CFR 820, ISO 13485, and EU MDR supplier control requirements. * Negotiate complex development agreements, commercial ...
Maintenance Technician - Stella (MDR)
$20.25 - $24.25/hr
ABOUT GREYSTAR Greystar is a leading, fully integrated global real estate platform offering expertise in property management, investment management, development, and construction services in ...
Maintenance Technician - Stella (MDR)
$20.25 - $24.25/hr
ABOUT GREYSTAR Greystar is a leading, fully integrated global real estate platform offering expertise in property management, investment management, development, and construction services in ...
Triage MDR escalations - assess severity, validate findings, and initiate the appropriate internal response workflow * Coordinate detection rule tuning and alert threshold adjustments to reduce false ...
Triage MDR escalations - assess severity, validate findings, and initiate the appropriate internal response workflow * Coordinate detection rule tuning and alert threshold adjustments to reduce false ...
Ensure packaging meets global regulatory and quality standards (FDA, MDR, ISO 11607, UDI, etc.). * Collaborate cross-functionally with Regulatory Affairs, Marketing, Engineering, and Manufacturing to ...
Ensure packaging meets global regulatory and quality standards (FDA, MDR, ISO 11607, UDI, etc.). * Collaborate cross-functionally with Regulatory Affairs, Marketing, Engineering, and Manufacturing to ...
Ensure packaging meets global regulatory and quality standards (FDA, MDR, ISO 11607, UDI, etc.). * Collaborate cross-functionally with Regulatory Affairs, Marketing, Engineering, and Manufacturing to ...
Ensure packaging meets global regulatory and quality standards (FDA, MDR, ISO 11607, UDI, etc.). * Collaborate cross-functionally with Regulatory Affairs, Marketing, Engineering, and Manufacturing to ...
Ensure packaging meets global regulatory and quality standards (FDA, MDR, ISO 11607, UDI, etc.). * Collaborate cross-functionally with Regulatory Affairs, Marketing, Engineering, and Manufacturing to ...
Ensure packaging meets global regulatory and quality standards (FDA, MDR, ISO 11607, UDI, etc.). * Collaborate cross-functionally with Regulatory Affairs, Marketing, Engineering, and Manufacturing to ...
Ensure packaging meets global regulatory and quality standards (FDA, MDR, ISO 11607, UDI, etc.). * Collaborate cross-functionally with Regulatory Affairs, Marketing, Engineering, and Manufacturing to ...
Ensure packaging meets global regulatory and quality standards (FDA, MDR, ISO 11607, UDI, etc.). * Collaborate cross-functionally with Regulatory Affairs, Marketing, Engineering, and Manufacturing to ...
Senior Regulatory Specialist
Santa Clara, CA · On-site
$49 - $54/hr
Review EU MDR DoC translations for accuracy and consistency. * Ensure adherence to Good Documentation Practices (GDP) across all deliverables. * Executes and tracks addendum labeling requests. Cross ...
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Senior Regulatory Specialist
Santa Clara, CA · On-site
$49 - $54/hr
Review EU MDR DoC translations for accuracy and consistency. * Ensure adherence to Good Documentation Practices (GDP) across all deliverables. * Executes and tracks addendum labeling requests. Cross ...
Mdr information
See California salary details
$18.27 - $22.88
4% of jobs
$22.88 - $27.50
3% of jobs
$27.50 - $32.11
0% of jobs
$32.11 - $36.73
7% of jobs
$38.02 is the 25th percentile. Wages below this are outliers.
$36.73 - $41.34
36% of jobs
$41.34 - $45.96
11% of jobs
$45.96 - $50.57
7% of jobs
$53.75 is the 75th percentile. Wages above this are outliers.
$50.57 - $55.19
9% of jobs
$55.19 - $59.81
10% of jobs
$59.81 - $64.42
9% of jobs
$64.42 - $69.04
4% of jobs
$18
$46
$69
How much do mdr jobs pay per hour?
As of Aug 22, 2026, the average hourly pay for mdr in California is $46.57, according to ZipRecruiter salary data. Most workers in this role earn between $38.17 and $55.77 per hour, depending on experience, location, and employer.
What is an MDR?
An MDR (Market Development Representative) is a sales professional responsible for identifying and qualifying potential leads for a company's products or services. They focus on early-stage prospecting, researching target markets, and engaging with potential customers to generate sales opportunities. MDRs work closely with sales and marketing teams to ensure a seamless handoff of qualified leads for further nurturing and closing. Their role is crucial in driving business growth by expanding the company's customer base.
What does a typical day look like for a Medical Device Reprocessing (MDR) technician?
A typical day for an MDR Technician involves cleaning, disinfecting, and sterilizing surgical instruments and medical devices according to strict protocols. You'll routinely inspect equipment, assemble instrument trays, document processes, and ensure all items meet quality assurance standards. MDR Technicians frequently collaborate with surgical teams and other healthcare professionals to meet tight turnaround times for critical instruments. This is a hands-on role that requires adaptability, precision, and a commitment to patient safety, often performed in hospital central sterile departments or specialized clinics.
What are the key skills and qualifications needed to thrive in the MDR position, and why are they important?
To thrive as a Medical Device Reprocessing (MDR) Technician, you need knowledge of sterilization processes, infection control standards, and a high school diploma or equivalent, often supplemented with formal MDR certification. Familiarity with autoclaves, washer-disinfectors, and tracking systems is necessary for proper equipment handling. Attention to detail, teamwork, and effective communication are important soft skills in this role. These abilities ensure patient safety and efficient support of clinical procedures in healthcare environments.
What are popular job titles related to Mdr jobs in California?
For Mdr jobs in California, the most frequently searched job titles are:
What job categories do people searching Mdr jobs in California look for?
The top searched job categories for Mdr jobs in California are:
What cities in California are hiring for Mdr jobs?
Cities in California with the most Mdr job openings:
Design Assurance Engineer - Orthopedic Medical Devices
San Francisco, CA • On-site
Contractor
Re-posted 10 days ago
Job description
Hi,
My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Design Assurance Engineer position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows.
Role: Design Assurance Engineer – Orthopedic Medical Devices
Location: California
Duration: Long Term
Position Overview
We are seeking an experienced Design Assurance Engineer to support EU MDR remediation and quality initiatives for orthopedic medical device product lines. This role will focus on design assurance activities, technical documentation remediation, risk management, and ensuring compliance with global regulatory requirements throughout the product lifecycle.
The ideal candidate will have a strong background in orthopedic medical devices, design controls, risk management, and EU MDR compliance within a regulated medical device environment.
Key Responsibilities
- Support EU MDR remediation projects for orthopedic medical device products.
- Review, update, and maintain Design History Files (DHFs) and technical documentation.
- Perform design assurance activities across all stages of the product lifecycle.
- Conduct risk management activities in accordance with ISO 14971 requirements.
- Execute gap assessments and remediation efforts to ensure EU MDR compliance.
- Participate in design reviews and support design control activities.
- Review and update verification and validation documentation.
- Collaborate with Regulatory Affairs, Clinical Affairs, Manufacturing, R&D, and Quality teams.
- Support regulatory submissions and responses related to EU MDR requirements.
- Ensure compliance with FDA regulations, EU MDR requirements, ISO 13485, and applicable quality standards.
- Drive quality and compliance improvements across product development and remediation initiatives.
Required Qualifications
- Bachelor's degree in Engineering or a related technical discipline.
- 5–10+ years of Design Assurance, Quality Engineering, or Medical Device Quality experience.
- Strong experience within the orthopedic medical device industry.
- Proven experience supporting design assurance, remediation, or quality engineering projects.
- Strong knowledge of:
- Design Controls
- Risk Management
- Product Lifecycle Management
- Technical Documentation
- Design History Files (DHFs)
- Working knowledge of:
- FDA 21 CFR Part 820
- ISO 13485
- ISO 14971
- EU MDR Regulations
- Experience working within cross-functional product development and quality teams.
- Excellent communication, technical writing, and documentation skills.
I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.
Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/
Thank you,
Karthik Mutyala
Recruiting Manager
Stark Pharma Solutions Inc
Email: karthik@starkpharma.com
15 Corporate Place S, Suite 350,
Piscataway, New Jersey 08854
www.starkpharma.com