Qureos Mentor

Medline Industries

<div><p><b>Job Summary
</b></p><p></p><p><b>Job Description
</b></p><p>JOB SUMMARY
<br>
Medline Industries is seeking a Senior Software Engineer with extensive experience in modernizing business systems using Java, microservices, AKS, and other modern technologies. The ideal candidate will have a proven track record of successful modernization projects, strong leadership skills, and the ability to work collaboratively with cross-functional teams.<br>
</p><p><br>
MAJOR RESPONSIBILITIES
</p><ul><li>Design, develop, and maintain highly scalable and reliable software solutions to modernize Medline systems using Java, microservices, AKS, and other modern technologies in Cloud.
</li><li>Collaborate with cross-functional teams to gather requirements, create technical specifications, and develop software solutions that meet business needs.
</li><li>Lead and mentor junior software engineers on the team, providing guidance on technical and professional development.
</li><li>Write clean, well-documented, and efficient code using software development best practices and ensure its robustness and scalability.
</li><li>Work with product owners to understand and prioritize business requirements and translate them into technical designs and implementations.
</li><li>Drive continuous improvement of software development processes, including code review, testing, and deployment strategies.
</li><li>Keep up to date with emerging trends and technologies in software development and apply them where appropriate.
</li><li>Troubleshoot and debug production issues as needed.
</li><li>Ensure software solutions are secure, scalable, and maintainable.
</li><li>Contribute to the overall architecture and design of application modernization.
</li></ul><p></p><p>MINIMUM JOB REQUIREMENTS
<br>
Education
</p><ul><li>Bachelor's in Computer Science, Software Engineering or related field.
</li></ul><p></p><p>Certification / Licensure
<br>
None required.<br>
</p><p><br>
Work Experience
</p><ul><li>At least 7 years of experience in software engineering, with a focus on application modernization.
</li></ul><p></p><p>Knowledge / Skills / Abilities
<br>
<br>
MINIMUM JOB REQUIREMENTS
</p><ul><li>At least 7 years of experience in software engineering, with a focus on application modernization.
</li><li>Strong experience with Java, microservices, AKS, and cloud technology.
</li><li>Experience with containerization and deployment tools such as Docker, Kubernetes, and Helm.
</li><li>Proven track record of successful software development projects and technical leadership.
</li><li>Experience with DevOps tools such as GitHub, Jenkins, and Terraform.
</li><li>Experience with test automation frameworks such as JUnit, Mockito, and Selenium.
</li><li>Strong understanding of database design and implementation.
</li><li>Excellent communication and collaboration skills, with a strong ability to work effectively in a team environment.
</li><li>Ability to work in a fast-paced, dynamic environment and adapt to changing priorities.
</li><li>Experience with front-end technologies such as React or Angular.
</li></ul><p></p><p>Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education &amp; training, and tremendous potential with a growing worldwide organization.
</p><p></p><p>The anticipated salary range for this position:
</p>$134,000.00 - $201,000.00 Annual
<p></p><p>The actual salary will vary based on applicant&rsquo;s location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.
</p><p></p><p>Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.
</p><p></p><p>We&rsquo;re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here .
</p><p></p><p>Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.</p></div><p></p>

Sr Software Engineer

<div><p><b>Job Summary
</b></p>This role is responsible for leading the clinical product surveillance and risk management teams. Management of the clinical product surveillance team will ensure that Medline&rsquo;s adverse event reporting strategy is compliant and aligned with FDA&rsquo;s requirements. Management of the risk management team will include ensuring that Medline&rsquo;s processes (such as design and post market surveillance) have adequate risk management requirements built in that align to ISO 14971.
<p></p><p><b>Job Description
</b></p><h2 class="jobSectionHeader"><b>Responsibilities:
</b></h2><ul><li><h2 class="jobSectionHeader"><b>Lead the corporate risk management team and clinical product surveillance teams. Develop and coach employees across all teams.
</b></h2></li><li><h2 class="jobSectionHeader"><b>Ensure that Medline is properly controlling risks on a global level for medical devices, OTC drugs, and cosmetics
</b></h2></li><li><h2 class="jobSectionHeader"><b>Ensure proper implementation if ISO 14971 requirements within Medline&rsquo;s Quality Management System
</b></h2></li><li><h2 class="jobSectionHeader"><b>Participate in and manage team members who participate in Health Hazard Evaluation (HHE) meetings and assist in recall and field action decisions
</b></h2></li><li><h2 class="jobSectionHeader"><b>Maintain compliance with 21 CFR Part 803 (Medical Device Reporting) and ensure Medline&rsquo;s MDR reporting strategy aligns with FDA requirements.
</b></h2></li><li><h2 class="jobSectionHeader"><b>Serve as the primary liaison with FDA as it relates to </b><b>recall and </b><b>adverse event communication
</b></h2></li><li><h2 class="jobSectionHeader"><b>Monitor and interpret regulatory changes related to field actions, adverse event requirements, and risk management, and ensure internal procedures are updated accordingly.
</b></h2></li><li><h2 class="jobSectionHeader"><b>Ensure timelines for all projects and deadlines are being met by the team. Provide routine updates to Management on team performance and progress on projects.
</b></h2></li><li><h2 class="jobSectionHeader"><b>Facilitate internal meetings with cross-functional teams and ensure alignment across stakeholders, including Sales Leadership and Divisional Leadership.
</b></h2></li></ul><h2 class="jobSectionHeader"><b>Management Responsibilities:
</b></h2><ul><li><h2 class="jobSectionHeader"><b>Typically manages through multiple Managers and/or Supervisors
</b></h2></li><li><h2 class="jobSectionHeader"><b>Oversee major projects/programs/outcomes
</b></h2></li><li><h2 class="jobSectionHeader"><b>Budget responsibility
</b></h2></li><li><h2 class="jobSectionHeader"><b>Interpret and execute policies for departments/projects; develop, recommend and implement new policies or modifications to existing policies
</b></h2></li><li><h2 class="jobSectionHeader"><b>Provide general guidelines and parameters for staff functioning
</b></h2></li><li><h2 class="jobSectionHeader"><b>Hiring staff, recommending pay increases, performing performance reviews, training and development of staff, estimating personnel needs, assigning work, meeting completion dates, interpreting and ensuring consistent application of organizational policies
</b></h2></li></ul><h2 class="jobSectionHeader"><b>Qualifications:
</b></h2><ul><li><h2 class="jobSectionHeader"><b>Bachelor&rsquo;s degree in Life Sciences, Engineering, Regulatory Affairs, or related field
</b></h2></li><li><h2 class="jobSectionHeader"><b>Minimum 7 years of experience in medical device regulatory compliance or quality assurance, with at least 3 years in recall management or clinical product surveillance.
</b></h2></li><li><h2 class="jobSectionHeader"><b>Deep understanding of FDA regulations including 21 CFR Part 7, Part 806, Part 803, ISO 14971, and ISO 13485.
</b></h2></li><li><h2 class="jobSectionHeader"><b>Proven experience managing complex recall events and regulatory submissions.
</b></h2></li><li><h2 class="jobSectionHeader"><b>Strong leadership, communication, and project management skills.
</b></h2></li><li><h2 class="jobSectionHeader"><b>Experience with FDA audits and internal quality audits.
</b></h2></li></ul><p></p><p>Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education &amp; training, and tremendous potential with a growing worldwide organization.
</p><p></p><p>The anticipated salary range for this position:
</p>$154,000.00 - $231,000.00 Annual
<p></p><p>The actual salary will vary based on applicant&rsquo;s location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.
</p><p></p><p>Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.
</p><p></p><p>We&rsquo;re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here .
</p><p></p><p>Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.</p></div><p></p>

Sr Manager Regulatory Compliance, Risk Management and Clinical

<div><p><b>Job Summary
</b></p>Provide clinical expertise and customer education programs, materials, and resources in support of Medline clinical products and/or services.
<br>
Provide end-user insight to clinical process enhancement and improvement opportunities in order to secure or enhance current business for area of specialty
<p></p><p><b>Job Description
</b></p><p><b>Responsibilities
</b></p><div><div><div><div><div><div><div><div><div><ul><li><p>Provide clinical support to customers and salesforce on clinical products and services.
</p></li><li><p>Call on potential and existing clinical customers within assigned territory (independently and in collaboration with Medline salesforce) to expand and retain business.
</p></li><li><p>Review account and product/service information and recommend formal, onsite educational programs to address clinical staff needs.
</p></li><li><p>Partner with sales force on product conversions and implementations. Assist sales in their territories as needed at the local and national/corporate account level.
</p></li><li><p>Conduct quarterly business reviews. Identify problem areas and recommend changes and solutions. Develop customer growth and retention service proposals through consultation and relationship building with key accounts.
</p></li><li><p>Coordinate, and present workshops and classes on clinical products and/or services. Develop clinical presentations and training on product lines
</p></li><li><p>Conduct quality investigations, waste assessments, clinical review &amp; observations for improved practice and best practice recommendations. Conduct clinical and utilization reviews to identify waste, standardization opportunities and clinical practice adjustments for programs of specialty area.
</p></li><li><p>Contribute to the development of new products along with the modification and improvements of existing products by providing customer (end user) insight for process enhancement and improvement opportunities.
</p></li><li><p>Engage in professional organizations; attend national, regional, and local industry events.
</p></li></ul><p><b>Work Experience
</b></p><ul><li><p>At least 5 years of clinical experience (patient care, education, or medical sales/support).
</p></li><li><p>Experience developing and delivering presentations/clinical information to various audience levels within an organization.
</p></li><li><p>Experience analyzing and reporting data in order to identify issues, trends, or exceptions to drive improvement of results and find solutions.
</p></li><li><p>Experience prioritizing workload and scheduling effectively in order to meet deadlines.
</p></li><li><p>Experience developing and delivering presentations to various audience levels within, and external to, an organization.
</p></li><li><p>Proficient in Microsoft Word, Excel, PowerPoint.
</p></li><li><p>Position requires travel up to 75% of the time for business purposes within the local geography. Limited overnight travel.
</p></li><li><p>Environment includes office setting and medical facilities.
</p></li><li><p>Position may require non-traditional work hours during in-services
</p></li></ul></div></div></div></div></div></div></div></div></div><p></p><p><b>Preferred Qualifications
</b></p><ul><li><p>RN License
</p></li><li><p>Healthcare supply chain or value analysis experience
</p></li></ul><p></p><p>Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education &amp; training, and tremendous potential with a growing worldwide organization.
</p><p></p><p>The anticipated salary range for this position:
</p>$92,000.00 - $138,000.00 Annual
<p></p><p>The actual salary will vary based on applicant&rsquo;s location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.
</p><p></p><p>Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.
</p><p></p><p>We&rsquo;re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here .
</p><p></p><p>Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.</p></div><p></p>

Senior Clinical Solutions Specialist

Join Medline Industries and explore 3   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Medline Industries

ABOUT_COMPANY

Sr Software Engineer

Sr Manager Regulatory Compliance, Risk Management and Clinical

Senior Clinical Solutions Specialist