MedTech Biomedical Quality Specialist

IQVIA; Dallas (TX); On-site; USD 40,000 - 57,000; Full time

Benefits offered by this job

Medical benefits

Job summary

IQVIA in the United States seeks an Experienced Quality/Regulatory Inspector willing to travel nationally each week to up to three sites. This one-year assignment may extend based on business needs and requires a valid Real ID driver’s license and prior Biomedical Technician or QA/Regulatory experience.

You’ll work with minimal supervision, meet hospital vendor credentialing requirements, and may need up-to-date immunizations. Expect 40 hours weekly with potential extra travel-based hours.

Qualifications

• 3+ years of Biomedical Technician or Quality/Regulatory experience.
• Previous experience with documentation in a heavily regulated environment.
• Must be able to meet all requirements for each hospital Vendor Credentialing service.
• Position may/will require up to date immunizations.

Responsibilities

• Weekly national travel with a maximum of 3 locations in a week.

Skills

Biomedical Technician experience

Quality/Regulatory experience

Documentation in regulated env

Work under minimal supervision

Flexible schedule

Tools

Microsoft Office Suite

Salesforce CRM

Job description

Atlanta, GA

Philadelphia, PA

Chicago, IL

Kansas City, MO

Dallas, TX

Full time

R1566290

Experienced Quality/Regulatory Inspector needed who’s willing to travel nationally each week. Number of weekly locations will differ but could include up to 3 separate sites. Previous related experience is required as well as a valid Driver’s License that is a Real ID. Currently looking at a one-year opportunity, with the chance of extension based on business needs.

Job Responsibilities

• Weekly national travel with a maximum of 3 locations in a week.

Schedule

• 40 hours/week
• Possibility for more depending on travel conditions.
• Should hours be less than 40 in a week due to scheduling and not applicant’s availability, IQVIA will provide supplemental hours to ensure a 40-hour timecard.

Required Qualifications

• 3+ years of Biomedical Technician or Quality/Regulatory experience.
• Previous experience with documentation in a heavily regulated environment.
• Ability to work under minimal supervision.
• Must be able to function under a flexible schedule.
• Must be able to meet all requirements for each hospital Vendor Credentialing service.
• Position may/will require up to date immunizations.

Preferred Qualifications

• Biomedical Technician experience is a plus.
• Previous experience with documentation in a heavily regulated environment.
• Experience with system auditing or software validation preferred.
• Experience with large data sets for validation preferred.
• Experience managing small teams to ensure quality work being completed preferred.
• Proven track record of customer service and client management.
• Microsoft Office Suite
• Salesforce CRM
• History of traveling for work while meeting/exceeding expectations.

Benefits

• This position is eligible for our Medical Benefits.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe

Note: This role is not eligible for visa sponsorship. Candidates must have authorization to work in the US without the need for sponsorship.

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

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

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.

The potential base pay range for this role is 35 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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

EEO Minorities/Females/Protected Veterans/Disabled