Quality Coordinator Visa Sponsorship Jobs in Massachusetts
Quality coordinator jobs in Massachusetts span the state's medical device, biopharma, and advanced manufacturing sectors, with major employers concentrated in Boston, Marlborough, and the Route 128 corridor. Companies like Boston Scientific, Raytheon Technologies, and Thermo Fisher Scientific have active quality and compliance functions that regularly support visa sponsorship for qualified candidates.
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Transplant Quality RN Coordinator - Boston
Tufts Medical Center is a world-renowned academic medical center that has been caring for patients across New England for more than 200 years. As the principal teaching hospital of Tufts University School of Medicine and a nationally respected research institution, we are known for delivering groundbreaking, patient-centered care across more than 100 specialties and services, from primary care to our Level I Trauma Center to the region’s leading heart transplant program.
Nurses are at the heart of that mission.
As a Magnet® designated organization, Tufts Medical Center offers nurses the opportunity to practice at the highest level grounded in teamwork, clinical inquiry, and a culture of continuous improvement. We are committed to advancing nursing through evidence-based care, shared decision-making, and strong interdisciplinary collaboration.
Nurses at Tufts MC are deeply integrated into all aspects of clinical care and operations. Whether providing high-acuity specialty care or leading quality and safety initiatives, our nurses are respected as full partners in care delivery and innovation. Their insight drives progress. Their expertise shapes outcomes. Individual contributor role that may direct the work of other lower level professionals or manage processes and programs.
Hours: 40 Hours per week, Day Shift
Job Profile Summary
This role focuses on developing and implementing programs to establish, maintain, and improve patient quality care standards. In addition, this role focuses on performing the following Performance Improvement/Quality duties: Identifies and executes performance improvement and quality opportunities across the enterprise, enabling successful transformations and driving cost savings, process and product quality, and achievement of business goals. Responsibilities also include partnering with business leaders to provide expert insight on existing processes and procedures, applies process improvement methodologies to achieve PI/Quality objectives, and builds process improvement capabilities. A professional individual contributor role that may direct the work of other lower level professionals or manage processes and programs. The majority of time is spent overseeing the design, implementation or delivery of processes, programs and policies using specialized knowledge and skills typically acquired through advanced education. An experienced level role that applies practical knowledge of job area typically obtained through advanced education and work experience. Works independently with general supervision, problems faced are difficult but typically not complex, and may influence others within the job area through explanation of facts, policies and practices.
Job Overview
This position develops, maintains, and supports execution of the Quality Management Plan and Quality Assessment and Performance Improvement (QAPI) Program for the Solid Organ Transplant and VAD Programs. This position collaborates with inpatient and outpatient clinical transplant and VAD teams, Medical and Surgical Directors, and operational leaders to identify improvement opportunities, implement evidence-based change, measure outcomes, and sustain improvements. The position supports quality assurance, patient safety, regulatory compliance, continuous survey readiness, and optimal patient outcomes.
Job Description
Minimum Qualifications:
- Bachelor of Science in Nursing (BSN).
- Current, unrestricted Registered Nurse (RN) license in the state of practice.
- Three (3) years of RN experience.
Preferred Qualifications:
- Master’s degree.
- Three (3) years of Transplant or Med/Surg RN Experience.
- Six (6) years of extensive work with healthcare technology and databases.
- Experience in QAPI, performance improvement, regulatory readiness, and patient safety within solid organ transplant, advanced heart failure, VAD, or another highly regulated clinical program.
- Experience in data analysis, audit methodology, root cause analysis, corrective action planning, and change management.
Duties and Responsibilities: The duties and responsibilities listed below are intended to describe the general nature of work and are not intended to be an all-inclusive list. Other duties and responsibilities may be assigned.
- Ensures compliance with all applicable state and federal regulatory, accreditation, and certification requirements, including Organ Procurement and Transplantation Network (OPTN) policies and membership requirements, Centers for Medicare & Medicaid Services (CMS) Conditions of Participation for transplant programs, and The Joint Commission Ventricular Assist Device (VAD) certification requirements.
- Supports development, implementation, evaluation, and sustainment of the Quality Management Plan and Quality Assessment and Performance Improvement (QAPI) Program for the Solid Organ Transplant and VAD Programs.
- Manages the document control process for policies, standard operating procedures, clinical protocols, QAPI plans, and regulatory evidence, ensuring timely review, approval, revision, implementation, and staff communication.
- Develops and completes scheduled and focused audits, tracers, gap analyses, and compliance monitoring; analyzes findings, identifies trends and improvement opportunities, and reports results to the Director of Quality and Regulatory and program leadership.
- Collaborates with inpatient and outpatient Solid Organ Transplant and VAD clinical teams to translate audit findings, quality data, and identified risks into effective performance improvement interventions and sustained practice change.
- Monitors and reviews patient safety reports, complaints, adverse events, near misses, and regulatory reportable events; supports case review, root cause analysis, failure mode and effects analysis, corrective action plans, and effectiveness monitoring.
- Supports preparation for QAPI and Morbidity and Mortality (M&M) meetings, including agenda development, case identification, case summaries, data validation, quality dashboards, minutes, action-item tracking, and follow-up.
- Develops and maintains systems to document staff qualifications, orientation, training, competencies, annual education, and continuing professional development required for regulatory and certification readiness.
- Supports continuous readiness for OPTN and CMS transplant surveys and The Joint Commission VAD certification reviews, including mock surveys, tracers, evidence-file preparation, gap remediation, and response to findings.
- Oversees Solid Organ Transplant and VAD quality databases and registries and performs data entry, validation, reconciliation, retrieval, analysis, and reporting to ensure data integrity and timely submission.
- Prepares and presents quality dashboards, outcome reports, audit findings, regulatory metrics, trends, benchmarks, and performance improvement updates for the Director of Quality and Regulatory, program leadership, QAPI, M&M, and governance committees.
- Supports required reporting and documentation for OPTN, CMS, and applicable VAD registries, including STS Intermacs, within required timeframes.
- Assists with Requests for Information (RFIs), payer quality reviews, designation applications, and other external requests requiring validated transplant and VAD quality or outcomes data.
- Supports safe onboarding of new therapies, technologies, and clinical processes by completing readiness assessments, risk reviews, education plans, post-implementation audits, and outcome monitoring.
- Maintains accurate meeting minutes, decision logs, corrective action plans, and follow-up documentation; tracks assigned actions through completion and verifies that improvements are sustained.
Physical Requirements:
- This is largely a sedentary role, which involves sitting most of the time, but may involve movements such as walking, standing, reaching, ascending/descending stairs, and operating office equipment.
- Frequently required to speak, hear, communicate, and exchange information.
- Ability to see and read computer displays, read fine print, and/or normal type size print and distinguish letters, numbers and symbols.
- Requires manual dexterity using fine hand manipulation to operate computer keyboard.
Skills & Abilities:
- Willingness to continue professional development through participation in relevant conferences, training and educational activities.
- Excellent written and oral communication skills.
- Strong analytical, critical-thinking, problem-solving, and change-management skills.
- Ability to conduct audits and tracers, analyze quality and outcomes data, facilitate QAPI initiatives, develop corrective action plans, and evaluate effectiveness.
- Proficiency with Microsoft Office and healthcare quality data, reporting, and visualization tools.
- Ability to work effectively across multidisciplinary inpatient and outpatient clinical teams in a high-performance, highly regulated environment.
At Tufts Medicine, we want every individual to feel valued for the skills and experience they bring. Our compensation philosophy is designed to offer fair, competitive pay that attracts, retains, and motivates highly talented individuals, while rewarding the important work you do every day.
The base pay ranges reflect the minimum qualifications for the role. Individual offers are determined using a comprehensive approach that considers relevant experience, certifications, education, skills, and internal equity to ensure compensation is fair, consistent, and aligned with our business goals.
Beyond base pay, Tufts Medicine provides a comprehensive Total Rewards package that supports your health, financial security, and career growth—one of the many ways we invest in you so you can thrive both at work and outside of it.
Pay Range:
$91,879.42 - $117,150.49based on full-time equivalent
Quality Coordinator Job Roles in Massachusetts
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Search Quality Coordinator Jobs in MassachusettsQuality Coordinator Jobs in Massachusetts: Frequently Asked Questions
Which companies sponsor visas for quality coordinators in Massachusetts?
Massachusetts employers with established visa sponsorship programs for quality roles include Boston Scientific, Thermo Fisher Scientific, Raytheon Technologies, Hologic, and Biogen. These companies maintain large quality and regulatory affairs teams across sites in Marlborough, Waltham, and the Greater Boston area. Firms with active H-1B visa Labor Condition Application filings in quality management functions are the most reliable indicators of genuine sponsorship capacity.
Which visa types realistically fit quality coordinator roles in Massachusetts?
Quality coordinator roles that require a bachelor's degree in a directly related field such as engineering, life sciences, or quality management can qualify as specialty occupations under the H-1B visa. The H-1B is subject to an annual cap and selection process. EB-2 and EB-3 employment-based green cards are also viable for longer-term sponsorship, typically requiring PERM labor certification. F-1 OPT and STEM OPT can bridge candidates into full sponsorship if the degree is STEM-designated.
How to find quality coordinator visa sponsorship jobs in Massachusetts?
Migrate Mate lists quality coordinator roles at Massachusetts employers with verified visa sponsorship history, searchable by city and industry. This is especially useful for narrowing down opportunities in the state's medical device and biopharma corridors around Boston, Marlborough, and Woburn. Filtering to employers with documented H-1B or green card filing activity saves significant time compared to applying broadly and discovering sponsorship availability only late in the process.
Which cities in Massachusetts have the most quality coordinator sponsorship jobs?
Boston and Cambridge anchor the state's biopharma and medical technology hiring, with quality coordinator demand concentrated among life sciences companies along the Route 128 and I-495 corridors. Marlborough is a notable hub due to Boston Scientific's large manufacturing and quality operations there. Waltham, Woburn, and Lexington also host significant quality and regulatory compliance teams at pharmaceutical and defense contractors with active sponsorship histories.
Are there state-specific factors that affect visa sponsorship for quality coordinators in Massachusetts?
Massachusetts has one of the highest concentrations of FDA-regulated manufacturers in the country, which drives steady demand for quality coordinators with formal credentials in quality management systems, ISO standards, or GxP environments. The state's university pipeline through schools like UMass Lowell and Northeastern produces candidates on OPT, and many employers in the life sciences sector are accustomed to sponsoring H-1B petitions for quality and compliance roles that meet the specialty occupation standard.
What is the prevailing wage for sponsored quality coordinator jobs in Massachusetts?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.