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Mdr Analyst Jobs in Georgia (NOW HIRING)

MLS Technologies

Embedded Firmware Engineer

Ball Ground, GA

$96K - $131K/yr

... analyzers Good communication skills, both written and oral Ability to work well both independently and as part of an integrated team Familiarity with the Medical Device Directive/Regulation (MDD/MDR ...

MLS Technologies

Embedded Firmware Engineer

Ball Ground, GA · On-site

$96K - $131K/yr

... analyzers * Good communication skills, both written and oral * Ability to work well both ... Familiarity with the Medical Device Directive/Regulation (MDD/MDR), ISO 13485, FDA design controls ...

Jobtailor

Senior Clinical Data Manager

Kennesaw, GA · On-site

$120 - $180/hr

Ensure data integrity and compliance with GCP, FDA, MDR/IVDR, and other applicable regulatory ... Advanced proficiency in data visualization tools and data analytics platforms (such as Python and ...

New

LivaNova

Regulatory & Clinical Specialist

Atlanta, GA · Remote

$85K - $95K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... EU MDR requirements. * Conduct systematic literature searches, appraisal, analysis, and summarization of data for state-of-the-art, safety and performance periodically. * Manage the overall ...

MBC Talent Connections

Process Technology Specialist

Albany, GA

$95K - $114K/hr

  • Medical

  • Dental

  • Vision

  • Retirement

Knowledge of medical device regulations (US FDA or EU MDR) * Proven validation experience Key ... Identify areas of risk, inefficiencies, and opportunities for improvement through data analysis and ...

New

Artivion

Senior Medical Writer

Kennesaw, GA · On-site

... MDR compliance * Collaborate with other departments to work as a team to accomplish tasks ... Generate interim analysis, investigator meeting slides, and final clinical study reports.

CryoLife

Senior Medical Writer

Kennesaw, GA · On-site

... MDR compliance * Collaborate with other departments to work as a team to accomplish tasks ... Generate interim analysis, investigator meeting slides, and final clinical study reports.

Acrisure, LLC

Security Incident Response Engineer

Atlanta, GA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Analyze alerts generated by EDR, SIEM, MDR, email security, cloud security, deception, and threat intelligence platforms. * Validate suspicious activity to distinguish true security incidents from ...

Acrisure

Security Incident Response Engineer

Atlanta, GA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Analyze alerts generated by EDR, SIEM, MDR, email security, cloud security, deception, and threat intelligence platforms. * Validate suspicious activity to distinguish true security incidents from ...

Acrisure

Security Incident Response Engineer

Atlanta, GA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Analyze alerts generated by EDR, SIEM, MDR, email security, cloud security, deception, and threat intelligence platforms. * Validate suspicious activity to distinguish true security incidents from ...

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Showing results 21-40

All JobsMdr Analyst JobsMdr Analyst Jobs in Georgia

Mdr Analyst information

See Georgia salary details

$32.9K

$58K

$82.3K

How much do mdr analyst jobs pay per year?

As of Aug 20, 2026, the average yearly pay for mdr analyst in Georgia is $57,972.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,700.00 and $58,300.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an MDR analyst?

To thrive as an MDR (Managed Detection and Response) Analyst, you need a solid understanding of cybersecurity principles, incident response, threat detection, and relevant IT infrastructure, often supported by a degree in cybersecurity, computer science, or related certifications like CompTIA Security+ or CISSP. Familiarity with security information and event management (SIEM) tools, endpoint detection and response (EDR) platforms, and ticketing systems is typically required. Strong analytical thinking, attention to detail, and effective communication skills help MDR Analysts investigate incidents and coordinate with stakeholders. These skills are crucial to quickly identify, assess, and mitigate security threats, minimizing risk and ensuring organizational resilience.

What are some common challenges faced by MDR analysts when investigating security incidents?

MDR Analysts often face challenges such as managing high alert volumes, distinguishing between false positives and genuine threats, and staying current with rapidly evolving attack techniques. The role requires quick decision-making and effective communication with clients or internal teams to coordinate responses. Analysts must balance investigative thoroughness with the need for timely action, often working under pressure during critical incidents.

What is the difference between Mdr Analyst vs Security Analyst?

AspectMdr AnalystSecurity Analyst
CredentialsCertifications like CompTIA Security+, CEH, CISSP (preferred)Certifications like CompTIA Security+, CISSP, GIAC Security Certifications
Work EnvironmentManaged Security Service Providers (MSSPs), cybersecurity firmsCorporate IT departments, security teams in various industries
ResponsibilitiesMonitoring security alerts, managing MDR tools, incident responseAnalyzing security threats, implementing security measures, incident investigation

Both roles focus on cybersecurity, but Mdr Analysts primarily work with managed detection and response services, while Security Analysts handle broader security strategies within organizations. The roles often overlap in skills and certifications, making them closely related but distinct in their operational focus.

What is an MDR analyst?

An MDR (Managed Detection and Response) analyst is a cybersecurity professional responsible for monitoring, detecting, and responding to security threats within an organization's network. They use security tools such as SIEM systems and threat intelligence to identify and mitigate cyber incidents, often working in a 24/7 environment and requiring knowledge of security protocols and incident response procedures.

What are popular job titles related to Mdr Analyst jobs in Georgia?

For Mdr Analyst jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Mdr Analyst jobs in Georgia look for?

The top searched job categories for Mdr Analyst jobs in Georgia are:

What cities in Georgia are hiring for Mdr Analyst jobs?

Cities in Georgia with the most Mdr Analyst job openings:

Mdr Analyst jobs near you
Infographic showing various Mdr Analyst job openings in Georgia as of August 2026, with employment types broken down into 80% Full Time, 7% Part Time, 10% Contract, and 3% Nights. Highlights an 80% Physical, 9% Hybrid, and 11% Remote job distribution, with an average salary of $57,972 per year, or $27.9 per hour.

Sr. Regulatory Affairs Specialist

Becton, Dickinson and Company

Covington, GA • On-site

Full-time

Posted 6 days ago

BD rating

7.2

Company rating: 7.2 out of 10

Based on 141 frontline employees who took The Breakroom Quiz

323rd of 491 rated machine equipment manufacturers

Job description

We are the people who give possibilities purpose
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
Job Description
Urology and Critical Care (UCC) is an established and trusted partner in urinary healthcare, developing complete solutions which optimize the urine drainage process in the Acute Care Hospital setting. The Senior Regulatory Affairs Specialist is responsible for preparation of U.S and CE marking submissions/registration activities, along with supporting all other geographical regions registrations. In addition, this position will help support RA management.
This role provides the flexibility to work on-site 4 days weekly in Covington, and remotely Friday on a weekly basis.
Key responsibilities will include:
  • Regulatory support through the product life cycle on product project teams (e.g., developing regulatory strategies, change control, timeline development, and reviewing submission related documents).
  • Prepare &/or revise STED technical files for CE marking activities and notified body interaction to support EU/MDR product maintenance, as required.
  • Provide support and guidance for post market activities including remedial actions, labeling.
  • Prepare and support 510(k) &/or change assessments, as required.
  • Limited travel required - 15%.

To be successful in this role, you will work independently by applying your written and analytical skills to create technical documents, in some cases to cover design changes and change notifications for BD's wide range of medical devices. You will also leverage your communication skills to work effectively with internal customers and team members as well as external auditors.
Minimum Requirements:
  • Education: Bachelor of Science (BS) degree required, preferably in a scientific discipline, engineering, or other regulated field.
  • Experience:
    • Minimum 4 years of Regulatory Affairs experience within the medical device industry.
    • Experience supporting product registration, regulatory compliance, and quality system activities for medical devices.
  • Technical Knowledge: Working knowledge of U.S. FDA regulations, including 21 CFR Part 820, and European Medical Device Regulation (EU MDR).
  • Experience with:
    • U.S., EU, and international product registration activities.
    • Medical device quality systems and regulatory compliance.
    • Preparation and submission of FDA 510(k) premarket notifications.
    • Development and maintenance of technical documentation, including STED/Technical Files.
    • Interactions with regulatory authorities and/or EU Notified Bodies.
  • Core Competencies:
    • Demonstrated ability to support products throughout the product lifecycle, including product development, design changes, and post-market activities.
    • Experience developing regulatory strategies, conducting change assessments, and managing regulatory deliverables and timelines.
    • Strong technical writing skills with the ability to prepare clear, accurate, and compliant regulatory submissions.
    • Ability to maintain confidentiality when handling regulatory, clinical, and business-sensitive documentation.
    • Strong organizational and project management skills with the ability to prioritize multiple projects and meet deadlines.
    • Self-motivated with the ability to work independently, exercise sound judgment, and take ownership of responsibilities.
    • Effective written and verbal communication skills with demonstrated success working on cross-functional teams.
  • Work Arrangement: Ability to work on-site in Covington 4 days per week with remote work on Fridays
  • Travel: Willingness to travel up to 15% as needed

Preferred Qualifications:
  • Education: BS degree specifically in a Scientific Field (such as Biology, Chemistry, Biomedical Engineering)
  • Certification: Regulatory Affairs Certification (RAC) from the Regulatory Affairs Professionals Society (RAPS)
  • Product Knowledge: Familiarity with Class II medical devices, particularly in the urology or acute care hospital setting
  • Advanced Skills:
    • Experience leading regulatory activities on cross-functional product development teams.
    • Ability to influence project teams and communicate regulatory risks and mitigation strategies.
    • Strong analytical skills for evaluating technical data and determining regulatory impact.
    • Excellent communication skills for interactions with regulatory authorities, Notified Bodies, auditors, and cross-functional stakeholders.

At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.
For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.
Why Join Us?
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive.
We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
To learn more about BD visit https://bd.com/careers.
Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.
Required Skills
Optional Skills
Primary Work Location
USA GA - Covington BMD
Additional Locations
Work Shift
US BD 1st Shift 8am-430pm (United States of America)

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About BD

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BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.

Industry

Medical equipment and supplies manufacturing and manufacturing

Company size

10,000+ Employees

Headquarters location

Franklin Lakes, NJ, US

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