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Mdr Jobs (NOW HIRING)

Arctic Wolf

Product Marketing Manager - MDR

$157K/yr

You leverage deep industry experience in cybersecurity and Managed Detection and Response (MDR) and strategic planning to develop an actionable vision and execute growth strategies for MDR. Who You ...

Actalent

Assoc MDR/Vigilance Spec - Exempt

Saint Paul, MN · On-site

$27 - $30/hr

Evaluate incoming product events to determine MDR and Vigilance reporting eligibility. Initiate complete regulatory reports for timely submission to FDA and other regulatory bodies. Determine if ...

Collabera

MDR/Vigilance Specialist

Moundsview, MN

Complete applicable Medical Device Reports (MDR) as required per internal policy & procedures and FDA regulations. Ensure complaint investigations are adequate, accurate, detailed and timely. Perform ...

At-Bay

Security Account Executive (MDR)

The ideal candidate has a proven track record of building successful go-to-market sales motions and pipeline at an early-stage startup, experience selling endpoint protection / MDR / xDR solutions ...

Woodgrain, Inc.

Len Mdr Machine Operator

Lenoir, NC · On-site

$15.50 - $18.25/hr

Len Mdr Machine Operator Posting Start Date: 5/11/26 Division: Woodgrain Millwork Posting Area: Operations + Manufacturing Job Location: Lenoir, NC Looking for stability? Join Woodgrain! We're ...

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How much do mdr jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for mdr in the United States is $47.19, according to ZipRecruiter salary data. Most workers in this role earn between $38.70 and $56.49 per hour, depending on experience, location, and employer.

What jobs pay 2000 a day?

High-paying jobs that can pay around $2,000 a day include specialized roles such as surgeons, anesthesiologists, corporate lawyers, and certain high-level consultants or traders. These positions typically require advanced education, certifications, significant experience, and often involve high-stakes environments or independent contracting. Earnings can vary based on location, workload, and industry demand.

What job makes $10,000 a month without a degree?

A Medical Device Representative (MDR) can earn $10,000 or more per month through commissions and sales bonuses, often without requiring a college degree. Success in this role depends on strong sales skills, industry knowledge, and building client relationships, with some positions offering high earning potential based on performance.

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 is an MDR job title?

An MDR (Managed Detection and Response) specialist is a cybersecurity professional responsible for monitoring, detecting, and responding to security threats in an organization's network. They use security tools like SIEMs and threat intelligence platforms and often work in 24/7 security operations centers (SOCs). Certifications such as CompTIA Security+ or GIAC can enhance job prospects in this role.

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 is an MDR in a job?

An MDR in a job context typically refers to a Managed Detection and Response specialist, responsible for monitoring, detecting, and responding to cybersecurity threats. They often work with security tools, analyze security alerts, and may hold certifications like CISSP or CompTIA Security+ to perform their duties effectively.

What is an MDR job?

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.

More about Mdr jobs
What cities are hiring for Mdr jobs? Cities with the most Mdr job openings:
What are the most commonly searched types of Mdr jobs? The most popular types of Mdr jobs are:
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Mdr jobs near you
Infographic showing various Mdr job openings in the United States as of June 2026, with employment types broken down into 77% Full Time, 6% Temporary, 11% Contract, and 6% Nights. Highlights an 61% In-person, and 39% Remote job distribution, with an average salary of $98,145 per year, or $47.2 per hour.

Medical Writer (Must Have EU MDR)

millenniumsoft

Franklin Lakes, NJ • On-site

Contractor

Posted 1 hour ago

Job description

Position : Medical Writer (Must Have EU MDR)
Location : Franklin Lakes, NJ
Duration : 12 Months Contract
Total Hours/week : 40.00
Description:
  • The Medical Writer in client Medical Pharmaceutical Systems Medical Affairs is responsible for the generation and development of documents relating to Clinical and Human Factors assessments, evaluations and post market surveillance summaries.
  • Within this role, the Medical Writer will write and update Clinical Development Plans, Human Factor Engineering (HFE) Reports and other associated clinical and Human Factors (HF) documents.
  • The medical writer is a pivotal role to ensure compliance with associated regulations and pivotal in ensuring that there is available evidence to support the safety and performance of the products designed, produced and manufactured by the company.
  • The Medical Writer will perform and document systematic literature reviews, critically evaluate identified data, and will interface with various members of the Medical Affairs team and with cross-functional team members in order to achieve high-quality clinical and Human Factors documents.
  • The Medical Writer is also responsible for the development or review of study-related documents, including Clinical and Human Factors study executive summaries and related power point presentations.
  • The Medical Writer will be an integral part of the global Medical Affairs team and will collaborate with Medical Affairs leaders, Clinical and HF program leaders, Clinical and HF specialists and other key associates.
  • The Medical Writer is also responsible for optimizing processes for clinical evaluation and investigation as they relate to medical writing.
  • This role requires great familiarity and application of the associated regulations and guidance, including MDR (2017/745), MDD, MEDDEV 2.7.1 Rev. 4 and other MEDDEV guidances, ISO 14155, 21 CFR 812.
  • This role will report to the Associate Director, Medical Affairs in Franklin Lakes, NJ.

Job Functions:
  • Create and update Clinical Development Plans in accordance to MEDDEV 2.7/1 Revision 4 and in alignment with EU MDR.
  • Contribute to the Summary of Safety and Clinical Performance in alignment with EU MDR.
  • Perform comprehensive systematic, documented literature reviews using various search engines in order to support the Clinical Evaluation, Post-market Clinical Follow-Up, awareness of current State of the Art as well as any ad hoc reports required.
  • Develop and manage CER project plans and timelines.
  • Serve as a subject matter expert on clinical aspects of Technical documentation.
  • Analyze available clinical evidence (data held by the manufacturer, published literature) to assist the Medical Affairs team with clinical development strategy.
  • Write and or edit clinical documentation, including but not limited to clinical development plans, HFE reports, Health Hazard Evaluations. Ensure high quality study documentation that is submission-ready for various regulatory agency and external distribution.
  • Support periodic and ad hoc assessments of device safety and efficacy in support of post-market surveillance and risk management objectives.
  • Write and/or support the development of manuscripts relating to clinical study data or clinical evidence for submission to peer-reviewed medical journals or congresses.
  • Work with medical professionals to ensure alignment with journal requirements for targeted manuscript submission.
  • Write and/or contribute to abstracts and submissions of clinical and HF data to various medical device congresses or symposia.
  • Work with Medical Affairs and cross functional associates to ensure high quality submissions and data integrity.
  • Contribute to the development and optimization of Medical Affairs SOPs.
  • Support and assist Medical Affairs team members in the generation of effective visual and written communication.
  • Required Knowledge, Skills and Abilities
  • Strong interpersonal and communication skills.
  • Excellent project management skills with the ability to deliver projects on timelines that support corporate and departmental goals and objectives.
  • Strong analytical and organizational skills as well as demonstrated ability to solve problems with innovative solutions.
  • Outstanding oral and written communication skills.
  • Proven experience performing literature reviews, analyzing data and communicating outputs. Experience working within a medical device or pharmaceutical organization in a Research & Development, Scientific and Medical Affairs, Clinical or Regulatory role.
  • Proficiency in using and navigating PubMed, Embase and other literature search engines. Experience in DistillerSR, EndNote and other literature review tools a plus.
  • Strong working knowledge of regulations and guidance relating to Clinical Affairs, including EU MDR (2017/745), EU MDD (93/42/EEC), MEDDEV guidances, including 2.7/1 Revision 4 and 2.12/2 Revision 2, ISO 14155, ICH guidance including E3 CSR, E6 (R2) GCP, and familiarity regulations/ guideline relating to Risk management (i.e. ISO 13485 and ISO 14971). Familiarity with FDA guidance documents related to Human Factors Engineering.
  • Demonstrated ability to work independently and as part of a team.
  • Ability to prioritize tasks in a fast-paced environment. Ability to work under urgent deadlines and flexibility to accommodate fluctuating timelines.
  • Ability to work with a minimum of supervision.
  • Ability to work in a team environment.
  • Advanced skills using Microsoft Office products such as Outlook, Word, Excel and PowerPoint.

Minimum Requirements:
  • Bachelors in a relevant discipline required. Master's degree or PhD preferred
  • 3 years of experience as a medical writer
  • 3 years direct experience working on clinical evaluations within the Medical Device industry.
  • Medical writing certification a plus

Experience:
  • literature search engines PubMed, Embase: 1 year (Required)
  • ISO 13485 and ISO 14971: 1 year (Required)
  • EU MDR (2017/745), EU MDD (93/42/EEC), MEDDEV guidance: 1 year (Preferred)

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