medical device specialist

<div>
 <strong>
  Company Description
  <br/>
  <br/>
 </strong>
 <em>
  <em>
   SGS is the world&rsquo;s leading Testing, Inspection and Certification company. We operate a network of over 2,500 laboratories and business facilities across 115 countries, supported by a team of 99,500 dedicated professionals. With over 145 years of service excellence, we combine the precision and accuracy that define Swiss companies to help organizations achieve the highest standards of quality, compliance, and sustainability.
   <br/>
   <br/>
  </em>
 </em>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Support planning and conduct management system audits in accordance with SGS procedures to enable delivery of assessment and certification services that meet customer requirements and appropriate accreditation standards.
  </li>
  <li>
   Assist in business development as required and provide specific technical support to expand the company&rsquo;s capability to offer valued services to customers.
  </li>
  <li>
   Conduct audits (either desk-based or on client&rsquo;s sites) in accordance with established procedures and approved plans, maintaining a high standard of service delivery
  </li>
  <li>
   Ensure completion of all assigned work and relevant documentation and upload into the SGS system in accordance with required procedures, deadlines and standards to fulfil customer expectations
  </li>
  <li>
   Provide accurate and timely reporting as required by line management to assist the planning and management of operations
  </li>
  <li>
   Ensure effective follow-up and timely close-out of non-conformities in accordance with established procedures
  </li>
  <li>
   Manage personal schedule to work efficiently and to meet target changeability requirements as defined by the Operations Manager
  </li>
  <li>
   Project-manage auditing teams, as appropriate, to maximize efficiencies, enhance client satisfaction and ensure compliance with standards
  </li>
  <li>
   Undertake personal professional development and ensure appropriate training records and personal logs are updated and submitted to the NB to maintain relevant auditor registrations and competency codes and relevant industry knowledge
  </li>
  <li>
   If required, to provide technical support and staff training to all parts of the business to enhance the service capability of the business
  </li>
  <li>
   Support business development activities as required (including follow up and/or referral of inquiries, sales visits, assistance at events, seminars, etc) to enable on-going growth of the business
  </li>
  <li>
   Maintain a full knowledge and understanding of SGS procedures and external approval criteria to allow efficient and effective technical reviews
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   University or technical college degree in one of the following:
  </li>
  <li>
   biology or microbiology
  </li>
  <li>
   chemistry or biochemistry
  </li>
  <li>
   computer and software technology
  </li>
  <li>
   electrical, electronic, mechanical engineering or bioengineering
  </li>
  <li>
   human physiology
  </li>
  <li>
   medicine
  </li>
  <li>
   pharmacy
  </li>
  <li>
   physics or biophysics
  </li>
  <li>
   4 years of professional experience in relevant field
  </li>
  <li>
   Relevant industry such as: medical device industry and subcontractors, in vitro diagnostic industry and subcontractors, Sterilization department or sterilization service provider
  </li>
  <li>
   Appropriate knowledge of conformity assessment procedures laid down in medical device regulation 2017/745, FDA, SFDA.
  </li>
  <li>
   Appropriate knowledge of medical devices quality management system ISO 13485:2016 and must hold IRCA approved ISO 13485:2016 lead auditor certification.
  </li>
  <li>
   Demonstrate 2 years working knowledge on MDT/MDN codes per Regulation (EU) 2017/ 2185 codes and 4 years of industrial working experience knowledge specifically for MDS 1005, MDS1006 &amp; MDS1010,
  </li>
  <li>
   Knowledge of the standards such as cleanroom ISO 14644 series, biological evaluation ISO 10993 series, sterilization standards (ISO 11135, ISO 11137), clinical investigation ISO 14155, risk management of medical devices ISO 14971, and Common specifications and guidance associated with the product covered by the MDA, MDN or MDS code per regulation (EU) 2017/ 2185).Knowledge on MDCG documents for medical devices.
  </li>
  <li>
   Knowledge of clinical evaluations of product categories covered by regulation (EU) 2017/ 2185 codes
  </li>
  <li>
   Knowledge of relevant products standards covered by the regulation (EU) 2017/ 2185 codes
  </li>
  <li>
   Must be able to demonstrate and excellent working knowledge of medical device management and regulatory systems, standards, and compliance/auditing techniques
  </li>
  <li>
   Effective interpersonal skills; able to develop good working relationships with people at all levels
  </li>
  <li>
   Willingness to learn and adapt to change &ndash; committed to continuous personal and professional development
  </li>
  <li>
   Must have a detailed understanding of the relevant medical device regulations for which audits reviews are being undertaken
   <br/>
   <br/>
  </li>
 </ul>
</div>


Medical Device Specialist

<div><b>Company Description</b><p><i><br>
SGS is the world&rsquo;s leading Testing, Inspection and Certification company. We operate a network of over 2,500 laboratories and business facilities across 115 countries, supported by a team of 99,500 dedicated professionals. With over 145 years of service excellence, we combine the precision and accuracy that define Swiss companies to help organizations achieve the highest standards of quality, compliance, and sustainability.</i></p><b><br>
Job Description</b><br>
<ul><li>
Support planning and conduct management system audits in accordance with SGS procedures to enable delivery of assessment and certification services that meet customer requirements and appropriate accreditation standards.</li><li>
Assist in business development as required and provide specific technical support to expand the company&rsquo;s capability to offer valued services to customers.</li><li>
Conduct audits (either desk-based or on client&rsquo;s sites) in accordance with established procedures and approved plans, maintaining a high standard of service delivery</li><li>
Ensure completion of all assigned work and relevant documentation and upload into the SGS system in accordance with required procedures, deadlines and standards to fulfil customer expectations</li><li>
Provide accurate and timely reporting as required by line management to assist the planning and management of operations</li><li>
Ensure effective follow-up and timely close-out of non-conformities in accordance with established procedures</li><li>
Manage personal schedule to work efficiently and to meet target changeability requirements as defined by the Operations Manager</li><li>
Project-manage auditing teams, as appropriate, to maximize efficiencies, enhance client satisfaction and ensure compliance with standards</li><li>
Undertake personal professional development and ensure appropriate training records and personal logs are updated and submitted to the NB to maintain relevant auditor registrations and competency codes and relevant industry knowledge</li><li>
If required, to provide technical support and staff training to all parts of the business to enhance the service capability of the business</li><li>
Support business development activities as required (including follow up and/or referral of inquiries, sales visits, assistance at events, seminars, etc) to enable on-going growth of the business</li><li>
Maintain a full knowledge and understanding of SGS procedures and external approval criteria to allow efficient and effective technical reviews</li></ul><br>
<b>
Qualifications</b><br>
<ul><li>
University or technical college degree in one of the following:</li></ul><ul><li>
biology or microbiology</li><li>
chemistry or biochemistry</li><li>
computer and software technology</li><li>
electrical, electronic, mechanical engineering or bioengineering</li><li>
human physiology</li><li>
medicine</li><li>
pharmacy</li><li>
physics or biophysics</li></ul><ul><li>
4 years of professional experience in relevant field</li><li>
Relevant industry such as: medical device industry and subcontractors, in vitro diagnostic industry and subcontractors, Sterilization department or sterilization service provider</li><li>
Appropriate knowledge of conformity assessment procedures laid down in medical device regulation 2017/745, FDA, SFDA.</li><li>
Appropriate knowledge of medical devices quality management system ISO 13485:2016 and must hold IRCA approved ISO 13485:2016 lead auditor certification.</li><li>
Demonstrate 2 years working knowledge on MDT/MDN codes per Regulation (EU) 2017/ 2185 codes and 4 years of industrial working experience knowledge specifically for MDS 1005, MDS1006 &amp; MDS1010,</li><li>
Knowledge of the standards such as cleanroom ISO 14644 series, biological evaluation ISO 10993 series, sterilization standards (ISO 11135, ISO 11137), clinical investigation ISO 14155, risk management of medical devices ISO 14971, and Common specifications and guidance associated with the product covered by the MDA, MDN or MDS code per regulation (EU) 2017/ 2185).Knowledge on MDCG documents for medical devices.</li><li>
Knowledge of clinical evaluations of product categories covered by regulation (EU) 2017/ 2185 codes</li><li>
Knowledge of relevant products standards covered by the regulation (EU) 2017/ 2185 codes</li><li>
Must be able to demonstrate and excellent working knowledge of medical device management and regulatory systems, standards, and compliance/auditing techniques</li><li>
Effective interpersonal skills; able to develop good working relationships with people at all levels</li><li>
Willingness to learn and adapt to change &ndash; committed to continuous personal and professional development</li><li>
Must have a detailed understanding of the relevant medical device regulations for which audits reviews are being undertaken</li></ul><br>
<b>
Additional Information</b><p><br>
#LI-Onsite</p></div>

Pharmazone Kuwait

<p><b>About Opportunity</b></p><p>A reputable international company is seeking a qualified and experienced professional to join its growing team supporting operations in <b>Kuwait and Qatar</b>.</p><p>This role is ideal for candidates with strong experience in <b>medical aesthetic devices</b> and a proven track record of working closely with <b>dermatology and aesthetic clinics</b>.</p><p><b>Position</b></p><p>Medical Aesthetic Devices Specialist</p><p><b>Key Responsibilities &ndash; Medical Aesthetic Devices Specialist</b></p><p><b>1. Technical Support &amp; Product Expertise</b></p><ul><li>Provide technical support and product guidance to dermatology and aesthetic clinics.</li><li>Demonstrate the proper use, features, and benefits of medical aesthetic devices.</li><li>Assist clinics in optimizing device performance and treatment outcomes.</li></ul><p><b>2. Clinical Training</b></p><ul><li>Conduct training sessions for doctors, dermatologists, and clinic staff on the proper use of aesthetic devices.</li><li>Ensure safe operation of equipment according to manufacturer guidelines and medical standards.</li><li>Provide hands-on demonstrations during device installation and clinical use.</li></ul><p><b>3. Installation &amp; Device Setup</b></p><ul><li>Coordinate and support the installation of aesthetic devices in clinics.</li><li>Ensure devices are properly configured, tested, and ready for operation.</li><li>Provide operational guidance to ensure smooth device integration into clinic workflows.</li></ul><p><b>4. Client Relationship Management</b></p><ul><li>Build and maintain strong relationships with dermatologists, clinic managers, and medical staff.</li><li>Act as the main technical contact for clinics using the company&rsquo;s devices.</li><li>Address client inquiries and provide solutions in a timely and professional manner.</li></ul><p><b>5. Troubleshooting &amp; Technical Follow-Up</b></p><ul><li>Identify and resolve basic technical issues related to device usage.</li><li>Coordinate with the technical or engineering team for advanced troubleshooting when required.</li><li>Follow up with clinics to ensure devices operate efficiently.</li></ul><p><b>6. Market &amp; Product Support</b></p><ul><li>Support the sales team during product presentations and demonstrations.</li><li>Participate in medical events, workshops, and conferences when required.</li><li>Provide feedback to management regarding market needs and clinical requirements.</li></ul><p><b>7. Compliance &amp; Safety</b></p><ul><li>Ensure all device usage complies with medical regulations, safety standards, and manufacturer protocols.</li><li>Maintain proper documentation related to installations, training, and technical visits.</li></ul><p><b>Key Requirements</b></p><ul><li>Minimum <b>5 years of experience</b> in medical aesthetic devices.</li><li>Proven experience supporting <b>dermatology and aesthetic clinics</b>.</li><li>Strong technical and product knowledge in aesthetic technologies.</li><li>Ability to build and maintain professional relationships with clinics and medical professionals.</li><li>Strong communication and presentation skills.</li><li>Willingness to travel between <b>Kuwait and Qatar</b> when required.</li></ul><p><b>What We Offer</b></p><ul><li>Attractive and competitive salary package.</li><li>Opportunity to work with a reputable international company.</li><li>Professional growth within a dynamic and expanding market.</li></ul><p><b>Availability</b></p><p>Immediate joiners are highly preferred.</p><p>Job Type: Full-time</p>

Medical Aesthetic Devices Specialist

IQVIA

<div><div><div>Saint Paul, United States of America | Part time | Field-based | R1533778</div><div><div><b>
Job available in additional locations</b></div></div></div><p></p><div><div><br>
The <b>Part Time Clinical Consultant (PTCC)</b> role is an exciting opportunity to join IQVIA. IQVIA/MedTech takes the approach to helping customers drive healthcare forward in this challenging, fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities.</div><div>
This part time position will be responsible for providing case support, patient management, and education to both new and existing accounts within an assigned client Franchise/Region.</div><div><b>
Duties and Responsibilities:</b></div><ul><li>
Acquire and demonstrate a working knowledge of our products/therapies and develop an understanding of their applications.</li><li>
Improve patient outcomes by delivering ventricular medical device education in a variety of settings, including but not limited to, the ICU, OR, and Cath Lab.</li><li>
Ventricular medical device case support, including on call support.</li><li>
Complete proactive rounds for patients receiving support and provide assistance.</li><li>
Collaborate with the Clinical Support Center (CSC) for ongoing additional support as necessary</li><li>
Maintain clinical competency in current product line, patient management, and remain up to date on most relevant information through continual learning and education</li><li>
Some travel may be needed</li></ul><div><b>
Job Qualifications:</b></div><ul><li>
Clinical certification required; Registered Nurse (RN)/Advanced Practice Provider (APP) license strongly preferred or relevant experience.</li><li>
3+ years&rsquo; experience with a strong clinical background in the Cardiac ICU (CICU), Cardiovascular ICU (CVICU), Cardiovascular OR (CVOR), or Catheterization Lab (Cath Lab) required; CVICU experience highly preferred.</li><li>
Some industry experience preferred, but not required.</li><li>
Significant experience with ventricular medical device is required (minimum of 10 cases/patients supported).</li><li>
Must provide a minimum of (2) days of live support within the field (case support, patient rounding, providing education), with a total of (5) days of availability per month.</li><li>
Availability must include (1) weekend per month.</li><li>
Ability to work on weekends, nights, holidays as well as weekdays.</li><li>
Ability to work at other hospitals aside from base location.
</li></ul><div>#LI-CES<br>
#LI-DNP</div><div>
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com</div><div>
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe</div><div>
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.</div>
The potential base pay range for this role is $60.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.</div></div><div></div>

MedTech Part Time Clinical Nurse Consultant – Milwaukee, WI

Abbott

<div><p>Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.</p><p><b>
Clinical Specialist I, CPT - Austin, TX</b></p><p></p><p><b>
Working at Abbott</b></p><p></p><p>
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You&rsquo;ll also have access to:</p><ul><li>
Career development with an international company where you can grow the career you dream of.</li><li>
Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year</li><li>
An excellent retirement savings plan with high employer contribution</li><li>
Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor&rsquo;s degree.</li><li>
A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.</li><li>
A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.</li></ul><p></p><p><b>
Neuromodulation</b></p><p></p><p>
Our Neuromodulation business includes implantable devices compatible with mobile technology to help people who suffer from chronic pain and movement disorders. These non-opioid therapies allow us to provide interventional pain therapy to patients throughout the pain continuum.</p><p></p><p><b>
The Opportunity</b></p><p></p><p>
Our team is actively recruiting for a <b>Clinical Specialist I, CPT</b> <b>in Austin, TX. </b>As a member of the clinical support team, is responsible for providing technical clinical expertise and support of the sales process to colleagues, current customers and/or potential customers. Works under general direction with clinical and sales teammates to identify and capitalize on sales opportunities by creating competency, comfort, and expertise with all Abbott Chronic Pain Therapies among physicians, support staff and customers within assigned geography. Performs work that involves a high degree of independence. Exercises independent judgment in planning, organizing, and performing work. Seeks to continually improve territory efficiency.</p><p></p><p><b>
What You&rsquo;ll Work On</b></p><ul><li>
Provides technical, clinical, and programming assistance, primarily in support of 1-2 Territory Manager(s).</li><li>
Assist Territory Managers in after-hours call support and activities.</li><li>
Integrates into all accounts, builds trust and relationships, and establishes strong rapport with customers.</li><li>
Proficient in complex programming, case support.</li><li>
Works seamlessly with Territory Manager(s) allowing them increased selling time.</li><li>
Will foster high trust relationships with customers, including the regional team members.</li><li>
Will begin to conduct PCP work and educational in services, as directed.</li><li>
As directed by sales manager, contacts, visits, and engages clients and potential clients in the Company&rsquo;s products and addresses any client questions and concerns.</li><li>
Provides medical professionals with sales support, information, and training on the use of Company products and with staff education, in-services, and technical troubleshooting.</li><li>
Develop and maintain an in-depth knowledge of assigned accounts and customers to include competitor activity.</li><li>
Conducts evaluations and develops sales strategies for capital equipment opportunities within accounts.</li><li>
Collects and studies information about new and existing products and monitors competitor sales, prices, and products.</li><li>
Provide feedback to providers both within operating room setting and outside operating room setting on the directions for use specific to implantable devices.</li><li>
May attend trade shows where new products and technologies are showcased and conferences to meet other sales representatives and clients and discuss new product developments.</li><li>
Uses clinical expertise to identify customer training and in-service needs with the goal of increasing customer usage, comfort and understating of all Abbott Chronic Pain Therapies product line.</li><li>
Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.</li><li>
Provides sales support, clinical in-services, training, and guidance to current or potential customers.</li><li>
Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.</li><li>
Performs other related duties and responsibilities, on occasion, as assigned.</li><li>
Ability to travel 25% within assigned region and/or outside assigned region.</li></ul><p><b><br>
Required Qualifications</b></p><ul><li>
Associates Degree or technical certification; preferred Bachelor&rsquo;s Degree.</li><li>
1 - 2 years&rsquo; work experience, strong preference collaborating with patients in clinical setting.</li><li>
The ability to communicate, understand and educate clinical data in the Chronic Pain Therapies space.</li><li>
Strong clinical skills.</li><li>
Excellent organizational, time management and prioritizing skills.</li><li>
Excellent interpersonal verbal, written and presentation skills with ability to effectively communicate at multiple levels and to large groups within and outside the organization.</li><li>
Capable of building strong working relationships with internal/external customers.</li><li>
Capable of working unpredictable schedule that may occasionally change on short notice due to operating room schedule changes and or delays.</li><li>
Accustomed to tight deadlines and managing multiple tasks.</li><li>
Strong sense of urgency.</li><li>
Ability to work in a highly matrixed and geographically diverse business environment.</li><li>
Ability to work within a team and as an individual contributor in a fast-paced, changing environment.</li><li>
Ability to leverage and/or engage others to accomplish projects.</li><li>
Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.</li><li>
Multitasks, prioritizes, and meets deadlines in timely manner.</li><li>
Capable of engaging customers in selling conversations as needed and as directed by Territory Manager.</li></ul><p></p><p><b>
Preferred Qualifications</b></p><ul><li>
Patient interaction experience within health care related environment (Physical Therapy, medical product sales, RN, LPN).</li><li>
Experience working in a broader enterprise/cross-division business unit model preferred.</li><li>
1-3 years&rsquo; experience with Abbott, or in similar spinal cord stimulation (SCS) setting or with another implantable medical device company.</li></ul><p></p><p><b>
Apply Now</b></p><p></p><p><b>
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: </b>www.abbottbenefits.com</p><p></p><p>
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.</p><p></p><p>
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews.</p><p><br>
The base pay for this position is $61,300.00 &ndash; $122,700.00. In specific locations, the pay range may vary from the range posted.</p></div>

Clinical Specialist I, CPT - Austin, TX

<div><div><div>Springfield, United States of America | Part time | Field-based | R1533573</div></div><p></p><div><div><br>
Our <b>MedTech Vascular Assistant</b> experiences a unique opportunity and leverage your clinical expertise in a dynamic role that goes beyond traditional patient care. Collaborate with healthcare professionals and advocate for the well-being of patients through medical device technology.</div><div><b>
What you will be doing in the role:</b></div><ul><li>
Supporting in-hospital case coverage on peripheral and/or coronary atherectomy cases.</li><li>
Demonstrate a high level of understanding in these types of situations through offering education and clinical knowledge to physicians performing the case/medical procedure.</li><li>
Per-diem schedule but can amount to 1- 2 days of work each week and can work with a current Part Time or Full-time</li><li>
Training for this role will be provided and is paid.</li></ul><div>
You will have an opportunity to travel, grow, and expand into new opportunities while earning supplemental income and learning the medical device industry.</div><div><b>
Job Requirements:</b></div><ul><li>
Active and unencumbered Radiology Technician (RT), RCIS, RN or Respiratory Therapist (RT) credential and licensure preferred</li><li>
Associates degree required, experience in leu of degree considered</li><li>
Hospital or industry experience required.</li><li>
Ability to clear hospital vendor credentialing requirements.</li><li>
Candidates must possess a valid driver&rsquo;s license and will be subject to a review of their driving record prior to hire.</li></ul><div><b>
Preferred Attributes:</b></div><ul><li>
Preferred unit or environment experience &ndash; Emphasis on Fluoroscopy, cardiac catheterization lab, interventional radiology, operating room, outpatient access center, ambulatory surgery center, ultrasound, or dialysis center.</li><li>
Leadership experience (manager, educator, preceptor) can be helpful but is not required.</li><li>
1 year experience preferred, Bachelor&rsquo;s degree preferred</li></ul><div>
IQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities.</div><div><b>
Benefits:</b> This position is not eligible for our Medical Benefits.</div><div><b>
Vaccine/Immunization/Hospital Credentialing Requirement:</b> A required function of this job requires individuals to enter various healthcare facilities. Thus, upon selection, individuals must complete healthcare facility credentialing process. To obtain credentials, individuals must meet the immunization requirements specified by the facility. Individuals are typically required to have completed/up to date: Measles, Mumps &amp; Rubella vaccine, Varicella (chicken pox) vaccine, Negative Tuberculosis (TB) Test, Tetanus, Diphtheria &amp; Pertussis (Tdap) vaccine, Hepatitis B vaccine, Influenza vaccine (seasonal), and COVID-19 vaccine primary series (heavily enforced by most facilities, some require booster(s)). Please note, IQVIA complies with all applicable laws regarding reasonable accommodations or exemptions for religious, medical, or other legally protected reasons, however, our client&rsquo;s requirements may supersede this.</div><ul><li><b>Please note:</b> Due to the nature of this role, it is not eligible for Visa sponsorship.</li></ul><div>
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com</div><div>
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe</div><div>
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.</div>
The potential base pay range for this role is 45-50 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.</div></div><div></div>

MedTech Vascular Assistant - Springfield, MA

CVRx, Inc.

<div><div><b>Why work for CVRx?</b></div>
<div>CVRx pioneers unique therapies that harness and harmonize the body's natural systems, benefiting society and making CVRx a universal role model in healthcare. We value our commitments to others and continue to overcome challenges through determination, collaboration, and purpose. If our culture and values speak to you, and if you have a passion for cutting-edge medical technologies, join our team and our mission to help others live better lives.</div>
<div></div>
<div><b>You must reside in the Columbia, SC metro areas to be considered for this remote job opportunity.</b></div>
<div></div>
<div>The Clinical Specialist at CVRx is responsible for providing clinical support for CVRx technology and business applications through education of current and potential customers, and procedure coverage within a defined region or geography, in partnership with Territory Managers, sales leaders and other key internal partners. As a Clinical Specialist at CVRx, you will play a vital role in supporting our cutting-edge technology while also supporting our commercial team in driving the expansion of our products.
</div><h3 class="jobSectionHeader"><b>Other duties and areas of responsibility include but are not limited to:
</b></h3><ul><li>Responsible for effectively communicating product and clinical benefits of Barostim therapy to cardiologists, heart failure/hypertension specialists, and cardiac/vascular surgeons to ensure their understanding of the therapy.</li>
<li>Facilitate trainings and other programs on proper application of Barostim therapy to clinicians, office, and hospital staff.</li>
<li>Provide technical support and troubleshooting during implant procedures, follow-up procedures, titrations, and patient office visits to ensure positive clinical outcomes.</li>
<li>Work with Territory Managers in developing effective plans to communicate the benefits of our technology, tailored to specific markets.</li>
<li>Work with Territory Managers, key physicians and site staff in the development and execution of a plan to effectively launch CVRx programs at new customer sites and ensure ongoing commitment to the program.</li>
<li>Drive utilization and continuous expansion of Barostim therapy through disease state education and supporting the development of therapeutic programs.</li>
<li>Act as a clinical interface between the medical community and the business.</li>
<li>Meet with existing and potential health care providers to identify their clinical needs, goals, and constraints related to patient care, providing creative and feasible solutions.</li>
<li>Adheres to sales management processes and reporting systems usage, including maintaining an accurate record of devices and programmers at all times in Salesforce.</li>
<li>Provide additional back-up support to other field staff as needed.</li>
</ul><h3 class="jobSectionHeader"><b>REQUIRED EDUCATION, TRAINING AND JOB-RELATED EXPERIENCE</b></h3><ul>
<li>Bachelor&rsquo;s degree or equivalent combination of education and experience</li>
<li>Strong interpersonal skills and ability to effectively manage relationships with key customer groups and CVRx staff.</li>
<li>Ability to master concepts of a medical and surgical nature, as well as that of active implantable medical device technology</li>
<li>Experience with products for cardiology or cardiac surgery therapeutic devices, heart failure experience will be prioritized</li>
<li>Independent, self-motivated, self-starter with the drive and persistence to introduce a novel and innovative technology to the market and support it becoming the standard of care</li>
<li>Must be detail-oriented and able to work independently</li>
<li>Proficient with Microsoft Office and ability to learn Salesforce, content management, learning management, and other systems as needed</li>
</ul><h3 class="jobSectionHeader"><b>PREFERRED EDUCATION, TRAINING AND JOB-RELATED EXPERIENCE</b></h3><ul>
<li>An advanced degree.</li>
<li>Healthcare experience beneficial</li>
<li>Knowledge of heart failure or cardiovascular market with clear understanding of competitive devices, strategies, advantages/disadvantages as they relate to the company&rsquo;s devices</li>
<li>Proficient with Microsoft Office and Salesforce, with the demonstrated ability to quickly learn content management, learning management and other systems as needed</li>
<li>Ability to interact with R&amp;D to represent customer perspective in order to provide input on product enhancements</li>
<li>and new product development</li>
</ul><h3 class="jobSectionHeader"><b>WORKING CONDITIONS</b></h3><ul>
<li>This position is remote-based and will require the candidate to live within the region specified.</li>
<li>This position will require interfacing with multiple internal departments and physician investigators/customers.</li>
<li>Must be able to lift up to 10 lbs.</li>
<li>Ability to travel 60% or more, some overnights may be required.</li>
<li>May be required to be fully vaccinated against the COVID-19 virus and other diseases.</li>
</ul><div>CVRx is proud to offer competitive salaries and benefits plans.</div>
<div></div>
<div>We offer a culture of teamwork, collaboration, and positivity, where challenging the status quo is welcomed, continuous learning is valued, and each of us has an opportunity to make a significant impact in an exciting, purpose-driven startup environment while also having fun.
</div>
<div></div><div>Salary range for U.S locations (USD): 100,000 - 120,000 per year.</div>
<div></div>
<div>The base salary range is applicable across the U.S., complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and specific location.
</div>
<div></div><div>In addition to Base Salary, this position is eligible for a Variable Incentive Plan (VIP) which provides the opportunity to earn additional variable compensation for meeting established objectives as outlined during first 30 days of employment.
</div>
<div></div><div>We also offer a competitive benefits package, details listed below:</div>
<div>Health &amp; Dental Insurance options with generous Company contributions
</div><div>Company contributions to an HSA if enrolled in a high deductible plan</div>
<div>401(k) with company match</div>
<div>Employee stock purchase plan &amp; stock option grants</div>
<div>12 company-paid holidays per year plus generous PTO plan</div>
<div>Paid time off for new parents</div>
<div>Company-paid life insurance &amp; disability</div>
<div>Unlimited growth opportunities</div>
<div>Training &amp; learning opportunities</div>
<div>Flexible Schedules</div>
<div></div>
<div>Compensation and benefits information pertains solely to candidates hired in the United States.
</div>
<div></div><div><b>EEO STATEMENT
</b></div><div>CVRx, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.</div>
<div>
</div><div>This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
</div>
<div></div><div>If you're an independent, self-motivated individual with excellent interpersonal skills, a desire to do great things and have a background in medical devices, healthcare or a related field, we want to hear from you!
</div>
<div></div><div>If you need assistance or an accommodation due to a disability, you may contact us at <b>hiring@cvrx.com</b></div>
<p>
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.</p></div>

Clinical Specialist - MedTech (Columbia, SC)

Search 10000+ Medical device specialist jobs near you this March. New roles added regularly across leading industries. Apply today.

10000 medical device specialist jobs Near Me

Medical Device Specialist

Medical Device Specialist

Medical Aesthetic Devices Specialist

MedTech Part Time Clinical Nurse Consultant – Milwaukee, WI

Clinical Specialist I, CPT - Austin, TX

MedTech Vascular Assistant - Springfield, MA

Clinical Specialist - MedTech (Columbia, SC)