qa specialist

CareCloud

<div></div><div><div>Department: MARKETING Experience: 2 YearsDeadline: May 31, 2026Location: Rawalpindi, Pakistan</div><div><h4 class="jobSectionHeader"><b>
Job Profile</b></h4><p></p><div><p><b>
Job Summary</b><br>
We are seeking a <b>Content QA Specialist</b> with strong knowledge of <b>medical and healthcare terminology</b> to review and ensure the accuracy, quality, and compliance of healthcare-related content before publication.</p>
<div><b>Key Responsibilities</b><br>
<ul><li>Review and proofread healthcare and medical content including blogs, ebooks, whitepapers, landing pages, and website copy.</li><li>Ensure accuracy of medical terminology, facts, statistics, and references used in the content.</li><li>Check grammar, spelling, readability, and clarity of content.</li><li>Ensure all content follows brand voice, editorial guidelines, and SEO best practices.</li><li>Verify sources and references for credibility.</li><li>Collaborate with writers and marketing teams to improve content quality.</li><li>Identify inaccuracies or inconsistencies and provide feedback for corrections.</li></ul></div><br>
<p></p>
</div><p></p><div><h4 class="jobSectionHeader"><b>
Tools / Skills</b></h4><p></p><div><ul><li>2&ndash;3 years of experience in content editing, proofreading, or quality assurance.</li><li>Strong knowledge of medical and healthcare terminology.</li><li>Excellent grammar, editing, and proofreading skills.</li><li>Familiarity with SEO content guidelines and digital publishing standards.</li><li>Strong attention to detail and analytical skills.</li></ul></div></div></div></div><p></p>
<br><div><h5 class="jobSectionHeader"><b>Additional Information</b></h5><div><div><p><b>
Total Position(s)
</b></p><p>1 Positions</p></div><div><p><b>
Gender</b></p><p>
Does not matter</p></div><div><p><b>
Minimum Education</b></p><p>
Bachelors Degree</p></div><div><p><b>
Degree Title</b></p><p>
Bachelors Degree</p></div><div><p><b>
Shift</b></p><p>
Evening</p></div><div><p><b>
Nature of Job</b></p><p>
Work From Office</p></div></div></div>

Content QA Specialist

Hologic

<div><p>Are you passionate about ensuring compliance and patient safety in the medical device industry? At Hologic, we are seeking a <b>Clinical QA Specialist</b> to play a critical role in the investigation and reporting of potential and actual adverse events, as well as other regulatory reporting activities. In this role, you&rsquo;ll collaborate with cross-functional teams, including Technical Service, Marketing, Sales, and Regulatory, to ensure timely and thorough documentation, analysis, and reporting. If you thrive in a fast-paced, collaborative environment and have a strong background in regulatory compliance and quality assurance, this is your opportunity to make a meaningful impact on healthcare innovation.</p>
<p><b>
Knowledge:</b></p>
<ul>
<li>Comprehensive understanding of FDA Quality System Regulations, ISO 13485, EU Medical Device Regulation, and ISO 14971 for risk management.</li>
<li>Strong knowledge of medical procedures and the expected and potential outcomes related to Hologic&rsquo;s product portfolio.</li>
<li>Familiarity with post-market surveillance requirements, adverse event reporting, and health risk assessments.</li>
<li>Awareness of regulatory reporting processes, including MedWatch reports, notified body communications, and external notifications.</li>
</ul>
<p><b>Skills:</b></p>
<ul>
<li>Proven ability to independently collect, analyze, and assess information associated with adverse events and determine appropriate next steps.</li>
<li>Effective communication skills to interact with internal teams, sales personnel, customers, patients, and regulatory agencies.</li>
<li>Strong organizational skills to ensure timely documentation, reporting, and follow-up of adverse events and regulatory submissions.</li>
<li>Analytical skills to support and lead investigations, including CAPAs, nonconformances, and other quality system processes.</li>
<li>Experience in developing metrics and quality reports related to reportable events and identifying potential excursions.</li>
<li>Ability to innovate and improve processes to enhance efficiency and compliance with post-market surveillance requirements.</li>
<li>Proficient in leading or participating in internal and external audits, inspections, and assessments.</li>
</ul>
<p><b>Behaviors:</b></p>
<ul>
<li>Proactive and detail-oriented, ensuring compliance with regulatory requirements and internal procedures.</li>
<li>Collaborative and team-oriented, fostering strong relationships across functions to support investigations and reporting activities.</li>
<li>Customer-focused, ensuring communications and responses are timely, accurate, and aligned with patient safety goals.</li>
<li>Resilient and adaptable, thriving in a fast-paced and evolving environment.</li>
<li>Problem-solving mindset, with a commitment to driving resolution and continuous improvement in quality processes.</li>
</ul>
<p><b>Experience:</b></p>
<ul>
<li>Bachelor&rsquo;s degree in Medicine, Nursing, Biomedical Engineering, Electromedical Engineering, or a related field. Risk Managers will also be considered.</li>
<li><b>5+ years</b> of experience in a similar role, preferably within the medical device or healthcare industry.</li>
<li>Hands-on experience with adverse event reporting, regulatory communications, and health risk assessments.</li>
<li>Proven track record in supporting or leading CAPAs, nonconformances, and quality investigations.</li>
</ul>
<p><b>Why join Hologic?</b></p>
<p>
We are committed to making Hologic the destination for top talent. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career.</p>
<p>
The annualized base salary range for this role is $83,000 - $129,700 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, education, business needs and market demand.</p>
<p><b>
Agency and Third-Party Recruiter Notice</b></p>
<p>
Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.</p>
<p><b>
Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.</b></p><br>
<p></p>
<p>
#LI-NT1</p></div>

Clinical QA Specialist

Nhan Hoa Comprehensive Health Care Clinic

<p><b>Summary:</b> The QI/QA Specialist for practice transformation will have primary responsibility for directing and managing clinical improvement initiatives of Nhan Hoa, ensuring regulatory compliance and promoting improved health care outcomes. The incumbent will work closely with the clinic&rsquo;s CMO and clinical team to establish a vision and direction for the quality improvement and quality assurance program within the framework of current regulations, market initiatives, existing program work plans and the network&rsquo;s strategic plan. The use of health information technology (electronic health records, patient portal, data repository, etc) and resulting data will be a major component of the QI/QA program.</p><p><b>Responsibilities:</b></p><ul><li>Designs and oversees implementation of clinical quality improvement and quality assurance programs with the guidance of the CMO.</li><li>Supports clinical team in developing and implementing the necessary teams, tools and team changes to improve patient outcomes and develop innovative approaches to primary care delivery reform.</li><li>Participate in critical analysis of individual center and network aggregate results of existing clinical outcome measures, while working closely with Nhan Hoa&rsquo;s clinical staff and informatics resource personnel to develop additional performance measures.</li><li>Routinely review provider charts for proper measures.</li><li>Make sure provider and clinic follow current up-to-date guidelines.</li><li>Works with Risk Manager to ensure the clinic is up to date on current credentialing</li><li>Review and prepare charts for routine internal auditing.</li><li>Assist with UDS and HRSA Quality measure</li><li>Review QI tools and surveys and provide technical assistance to staff</li><li>Review and analyze patient satisfaction survey.</li><li>Coordinating tracking and reporting of clinical outcomes, and follow-up of corrective action plans</li><li>Assist in development, monitoring, and presenting internal quality measures</li><li>Prepare QI reports and organize monthly QI/QA meeting</li><li>Works closely with Nhan Hoa staff to ensure that all clinical setup and workflow development is aligned with QI/QA program requirements, goals and objectives.</li><li>Participates in on-going development of clinical data repository and dashboard reporting. Participates in monthly QI/QA meetings and perform requested follow-up duties.</li><li>Assists with annual UDS and OSHPD reports. Assist with annual FTCA application related to QI.</li><li>Assist planning and development of PCMH activities, including working with PCMH team to develop content of PCMH Learning Sessions and webinars, and managing all aspects of these and other PCMH learning activities.</li><li>Provides oversight, direction, and support for quality improvement and care management staff in their efforts to support practice transformation with PCMH practices.</li><li>Provides expert advice to PCMH program leaders on the development, communication and implementation of key issues related to PCMH, including:</li><li>Clear vision and strategy on how practices will successfully transform to PCMH model</li><li>Expected timeline for practice participants to implement agreed upon strategy</li><li>Develops and supports positive and engaged team culture.</li><li>Identifies and manages staffing for additional program needs as needed.</li><li>Conducts ongoing staff performance evaluations.</li><li>Other activities and policies that support effective and measurable practice transformation.</li><li>Produces summary program reports summarizing key goals, accomplishments, and outcomes.</li><li>Stays abreast of new developments and industry trends related to PCMH, clinical quality improvement, and other assigned program(s).</li><li>Works with other relevant provider organizations and statewide groups, as applicable, to coordinate and align quality improvement efforts.</li><li>Performs other duties and responsibilities as requested</li></ul><p><b>Minimum Qualifications: </b></p><ul><li>Experience working in healthcare strongly preferred</li><li>Bachelor&rsquo;s degree in health or related field, licensed health care professional preferred.</li><li>In-depth understanding and minimum 3 years&rsquo; direct experience in using clinical quality improvement models and methods (e.g., Planned care Model, PCMH, rapid cycle improvement, quality measurement and reporting, clinical microsystems improvement).</li><li>Experience in program design, implementation and evaluation. Extensive knowledge and experience with industry-leading quality improvement methods and tools.</li><li>5. Excellent program management skills with demonstrated experience in managing wide range of clinical and/or administrative programs with excellent organizational skills.</li><li>Ability to work both independently and to collaborate with teams of individuals in diverse settings, with solution-oriented approach. Ability to deal effectively with a variety of people and work in a team environment.</li><li>Knowledge of computer software, including Microsoft Office.</li><li>Excellent written and verbal communication skills. Strong organizational skills with the ability to multi-task.</li><li>Data Analytics experience a plus</li><li>Ability to maintain detailed and confidential records</li></ul><p>Pay: $31.00 - $36.00 per hour</p><p>Benefits:</p><ul><li>401(k)</li><li>AD&amp;D insurance</li><li>Dental insurance</li><li>Health insurance</li><li>Life insurance</li><li>Paid time off</li><li>Parental leave</li><li>Retirement plan</li><li>Vision insurance</li></ul><p>Application Question(s):</p><ul><li>Do you have experience working in healthcare?</li><li>Do you have experience working with non-profits or FQHC?</li></ul><p>Education:</p><ul><li>Bachelor's (Required)</li></ul><p>Experience:</p><ul><li>QI/QA : 1 year (Required)</li></ul><p>Ability to Commute:</p><ul><li>Garden Grove, CA 92841 (Preferred)</li></ul><p>Willingness to travel:</p><ul><li>25% (Preferred)</li></ul><p>Work Location: In person</p>

QUALITY IMPROVEMENT/QUALITY ASSURANCE (QI/QA) SPECIALIST

World Central Kitchen

<div><p><b>About World Central Kitchen</b></p><p>
Founded in 2010 by Chef Jos&eacute; Andr&eacute;s, World Central Kitchen (WCK) is an international nonprofit organization that is first to the frontlines, providing fresh meals in response to disasters and crises. WCK has served more than 450 million meals by leveraging local resources and adapting in real time when disasters strike.</p><p><b>
Role Overview</b></p><p>
A World Central Kitchen (WCK) Culinary QA Specialist based in Egypt will serve as the dedicated culinary presence on the ground to safeguard the quality of food procurements destined for Gaza field kitchens. This contract role bridges the WCK Supply Chain &amp; Procurement team in Egypt with the Culinary Unit Manager in Gaza, ensuring that every product inspected, approved, and dispatched meets the standards required to serve dignified, culturally appropriate meals under crisis conditions.
</p><p>This position is a <b>three (3) month fixed-term contract</b> and reports directly to the Regional Culinary Manager, MENA.</p>
What You Will Do<p><b><i>
Quality Inspection &amp; Vendor Oversight</i></b></p><ul><li>
Conduct regular quality inspections at vendor facilities, cold stores, warehouses, and packaging sites across Egypt.</li></ul><ul><li>
Evaluate incoming and outgoing food products &mdash; frozen goods, canned proteins,grains, dried goods, and commodities &mdash; against WCK quality specifications.</li><li>
Perform sensory evaluations (taste, smell, texture, appearance) for all applicable product categories.</li><li>
Identify and document quality deficiencies including brand inconsistencies, incorrect specifications, packaging defects, and non-conforming products.</li></ul><p><b><i>
Pre-Dispatch Cargo Inspection</i></b></p><ul><li>
Inspect all cargo loads prior to dispatch to Gaza, verifying product quality, correct quantities, accurate labelling, and cold-chain integrity.</li><li>
Flag and formally escalate any non-conformities to the Supply Chain Manager and Culinary Unit Manager before dispatch is authorised.</li><li>
Ensure that rejected or flagged products are not dispatched until issues are</li><li>
resolved or replaced.</li></ul><p><b><i>
Vendor Engagement &amp; Feedback</i></b></p><ul><li>
Communicate WCK culinary standards, taste preferences, and quality expectations directly to vendor teams.</li><li>
Provide structured, documented feedback to vendors on product performance &mdash;taste, texture, consistency, and adherence to agreed specifications.</li><li>
Support the qualification of new vendors and products through organised tasting and evaluation sessions.</li><li>
Build professional relationships with vendor representatives to foster a culture of accountability and continuous improvement.</li></ul><p><b><i>
Coordination &amp; Reporting</i></b></p><ul><li>
Maintain close communication with the Culinary Unit Manager, Gaza, to stay aligned with kitchen needs, menu requirements, and Palestinian/Gazan culinary standards.</li><li>
Liaise regularly with the Supply Chain Manager on procurement schedules, vendor visits, and quality action items.</li><li>
Submit weekly quality inspection reports to the Regional Culinary Manager covering all inspections, issues identified, and actions taken.</li><li>
Maintain an ongoing product quality log tracking approvals, rejections, and vendor performance by category.</li></ul><br>
<b>
Requirements</b><br>
<ul><li>
Professional culinary background with a minimum of 3&ndash;5 years of experience in a professional kitchen, food production, or food quality environment.</li><li>
Familiarity with Palestinian and Gazan cuisine is strongly preferred and considered a significant advantage for this role.</li><li>
Arabic fluency required; working-level English for written reporting.</li><li>
Based in Cairo or able to relocate to Cairo for the duration of the contract.</li><li>
Willingness to conduct regular vendor site visits across the greater Cairo area.</li><li>
Detail-oriented, assertive in quality standards, and a clear and professional communicator.</li><li>
Prior experience with a humanitarian organisation or NGO food operations is an asset but not required.</li></ul><p><b>
Working Conditions</b></p><p>
This role requires the ability to work in high-stress, ambiguous environments with a focus on quality under operational pressure. Regular travel to vendor sites across Cairo is required. Flexibility and adaptability to changing conditions are essential.</p><p><b>
Contract Duration: </b>This is a three (3) month fixed-term contract with the possibility of extension based on operational need and performance.
</p><p><b>Contract Pay Rate:</b> $105 per day in local currency</p><b><br>
Benefits</b><p><b><br>
Why Join Us?</b></p><ul><li>
High-impact role directly supporting humanitarian food operations in Gaza.</li><li>
A collaborative working environment with WCK's experienced field and culinary teams.</li><li>
Opportunity to shape food quality standards in one of the world's most significant humanitarian responses.</li></ul><p><b>
Equal Opportunity</b></p><p>
WCK is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Join us in being a part of WCK's global talent journey!</p></div>

Culinary QA Specialist (Gaza Field Operations), Contract

dsm-firmenich

<div><p><b>QA/QC Specialist</b></p><p><b>
Gebze (Kocaeli), Turkey</b></p><p><b>
Onsite, Temporary for 16 months</b></p><p></p><p><br>
Join our Quality team as a QC/QA Specialist, where you will play a critical role in safeguarding product quality across our value chain. In this role, you will combine hands‑on analytical laboratory work with Quality Assurance activities, supporting production, supply chain, and customers while ensuring compliance with international quality standards. This is a challenging and rewarding position offering exposure to advanced analytical techniques and quality systems in a global manufacturing environment.</p><p></p><p><b><br>
Your key responsibilities</b></p><ul><li>
Perform or implement complex analytical testing methods using advanced techniques (e.g. GC/MS, HPLC/MS, NMR, IR) and routine quality control analyses</li><li>
Ensure accurate documentation, review of test results, and reporting against specifications</li><li>
Support qualification, calibration, and validation of laboratory equipment and analytical methods</li><li>
Participate in deviation investigations, root cause analysis, and continuous improvement activities</li><li>
Support Quality Assurance processes including audits, SOP preparation, training (GMP, SOPs), and product release activities</li><li>
Contribute to maintaining and improving ISO, HACCP, GMP, GLP, and FAMI‑QS compliant quality systems</li><li>
Follow up of yearly analysis plan, check of supplier documents as a part of raw material QC monitoring plan</li></ul><p></p><p><b><br>
We offer</b></p><ul><li>
A rich history and a promising future of bold scientific innovation and passionate creation with our customers</li><li>
A space to grow by encouraging and supporting curiosity and an open mindset</li><li>
A culture that prioritizes safety and well-being, both physically and mentally</li><li>
The opportunity to work for a company where sustainability is much more than a claim and is core to our strategy and purpose;</li><li>
A firm belief that working together with our customers is the key to achieving great things</li><li>
An eagerness to be one team and learn from each other to bring progress to life and create a better future;</li></ul><p></p><p><b><br>
You bring</b></p><ul><li>
Bachelor&rsquo;s degree in chemistry, analytical chemistry, or a related engineering/science field</li><li>
3&ndash;5 years of experience in Quality Control and/or Quality Assurance within a manufacturing or laboratory environment</li><li>
Strong knowledge of analytical techniques and best laboratory practices (GLP)</li><li>
Good understanding of quality management systems and standards (ISO, GMP, HACCP, Feed/Food/Pharma)</li><li>
Strong problem‑solving skills, attention to detail, and ability to work with complex data</li></ul><p></p><p><b><br>
Our application process</b></p><p>
Interested in this role? Then please apply online only via our career portal.</p><p>
Recruiter: Aylin Toy</p><p></p><p><b><br>
About ANH</b></p><p>
ANH, in the process of separating from dsm-firmenich, is a global leader in animal nutrition and health, as well as vitamins, carotenoids, and aroma ingredients - driven by its strong purpose: feeding the planet without costing the earth. Together, we make it possible. www.dsm-firmenich.com/ANH</p><p></p><p><b><br>
About dsm-firmenich</b></p><p>
At dsm-firmenich, we don&rsquo;t just meet expectations &ndash; we go beyond them.</p><p>
Join our global team powered by science, creativity, and a shared purpose: to bring progress to life.</p><p>
From elevating health to making fortified food and sustainable skincare, the impact of your work here will be felt by millions &ndash; every single day. Whether it&rsquo;s fragrance that helps you focus, alternative meat that&rsquo;s better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere.</p><p>
And while you&rsquo;re making a difference, we&rsquo;ll make sure you&rsquo;re growing too. With learning that never stops, a culture that lifts you up and the freedom to move across businesses, teams, and borders. Your voice matters here. And your ideas? They&rsquo;re essential to our future.</p><p>
Because real progress only happens when we<b> go beyond, together.</b></p><p></p><p><b><br>
Inclusion, belonging and equal opportunity statement</b></p><p>
At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work &ndash; and that&rsquo;s exactly the kind of culture we&rsquo;re building. A place where opportunity is truly equal, authenticity is celebrated, and everyone has the chance to grow, contribute, and feel they belong.</p><p>
We&rsquo;re proud to be an equal opportunity employer, and we&rsquo;re serious about making our hiring process as fair and inclusive as possible. From inclusive language and diverse interview panels to thoughtful sourcing, we&rsquo;re committed to reflecting the world we serve.</p><p>
We welcome candidates from all backgrounds &mdash; no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you.</p><p>
And if you have a disability or need any support through the application process, we&rsquo;re here to help &ndash; just let us know what you need, and we&rsquo;ll do everything we can to make it work.</p><p></p><p><b><br>
Agency statement
</b></p><p>We&rsquo;re managing this search directly at dsm-firmenich. If you&rsquo;re applying as an individual, we&rsquo;d love to hear from you. We&rsquo;re not accepting agency submissions or proposals involving fees or commissions for this role.</p></div><p></p>

QA/QC Specialist

OneOncology

<div><div><div><div><div><div><div><div><p>OneOncology is positioning community oncologists to drive the future of cancer care through a patient-centric, physician-driven, and technology-powered model to help improve the lives of everyone living with cancer. Our team is bringing together leaders to the market place to help drive OneOncology&rsquo;s mission and vision.</p></div></div></div></div></div></div></div><p></p><p>
Why join us? This is an exciting time to join OneOncology. Our values-driven culture reflects our startup enthusiasm supported by industry leaders in oncology, technology, and finance. We are looking for talented and highly-motivated individuals who demonstrate a natural desire to improve and build new processes that support the meaningful work of community oncologists and the patients they serve.</p><p></p><p><b>
Job Description:</b></p><p>
The <b>RCM QA Coding Specialist</b> is responsible for performing quality reviews of onshore and offshore billers and coders, and presenting findings to OneOncology and their partner practices, including physicians. This role is responsible for supporting practices in coding and auditing as well as education.</p><h2 class="jobSectionHeader"><b>
Responsibilities</b></h2><ul><li><p>
Conduct quality reviews of onshore and offshore billers and coders, to ensure accuracy and compliance with federal, state, and payer-specific regulations, while following industry standards and best practices.</p></li><li><p>
Conduct targeted quality reviews in alignment with the annual OIG Strategic Plan and provide detailed reports of audit outcomes to RCM Leadership and Compliance.</p></li><li><p>
May be required to conduct focused and random quality reviews in response to issues identified by industry trends and standards.</p></li><li><p>
Conduct pre-bill, performance improvement, and established coder quality reviews and provide education and training as necessary for coders to meet 95% accuracy rate.</p></li><li><p>
Analyze data, prepare reports and dashboards, and present review findings to OneOncology RCM leadership and partner practices, including physicians.</p></li><li><p>
Develop educational materials and provide training to staff based on quality review outcomes under the direction of the RCM Quality Review Manager.</p></li><li><p>
Effectively apply and disseminate current billing and coding regulations, auditing, and professional standards.</p></li><li><p>
Collaborate and partner with leadership, compliance, and risk management teams to ensure compliance with all federal, state and local regulations.</p></li><li><p>
Effectively abstract code procedural services for multiple specialties including imaging, medical oncology, pathology and E/M.</p></li><li><p>
Other duties as assigned to help drive our mission of improving the lives of everyone living with cancer.</p></li></ul><h2 class="jobSectionHeader"><b>
Qualifications</b></h2><ul><li><p>
CPC or other coding certification required</p></li><li><p>
CPMA certification preferred</p></li><li><p>
3+ years of medical auditing experience required</p></li><li><p>
E/M coding experience required</p></li><li><p>
Oncology coding experience preferred</p></li><li><p>
Strong communication and interpersonal skills</p></li><li><p>
Proficiency with Microsoft Office products</p></li><li><p>
Ability to work independently and collaboratively in a team environment</p></li><li><p>
Ability to meet deadlines</p></li><li><p>
Demonstrated success in using data to make decisions and drive behavior change to support organizations</p></li></ul><p></p><p>
#LI-REMOTE</p><p>
#INDOneOnc</p></div>

QA Coding Specialist

Dana-Farber Cancer Institute

<div><div><div><div>Job Ref:</div><div>
JR-3257</div></div><br>
<div><div>Location:</div><div>
450 Brookline Ave, BOSTON, MA 02215</div><br>
</div>
<div><div>Category:</div><div>
Quality/Risk Management/Patient Safety</div></div><br>
<div><div>Employment Type:</div><div>
Full time</div></div><br>
<div><div>Work Location:</div><div>
Remote: occasional onsite</div></div><br>
<div></div><div><div>Salary/Pay Rate:</div><div>
$76,900.00 - $86,100.00 per year</div>
</div></div><p><b>Overview</b></p>
<p></p><div><div>The QA/QI Specialist is responsible for monitoring operations and developing and managing quality improvement initiatives to ensure that systems are safe, effective, appropriate, compliant, current and adhered to by staff in the assigned unit or department. Expected to understand and principles of quality management practices to the monitoring and improvement of the operations for the unit(s) assigned. Key areas of focus may include patient and staff safety, clinical laboratory, cell processing, donor blood product collections, tissue banking, clinical operations, and other specified departmental procedures and policies as assigned. Plays key role in supporting preparation and on site support during site surveys and audits by regulatory agencies. Works with multidisciplinary teams and may be assigned to work under the direction of physician or nursing staff for assigned initiatives.<br>
ing knowledge of area assigned, carries out monitoring, documentation review, data gathering and some limited data analysis, basic audits, and support for quality improvement initiatives. Supports multidisciplinary teams in developing and carrying out quality improvement initiatives as assigned.<p>
Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals.</p><p><br>
 <b>PRIMARY DUTIES AND RESPONSIBILITIES:
</b></p><ul><li><p>ing significant knowledge of area assigned, carries out or leads monitoring efforts and populates dashboard and key indicator data sets</p></li><li><p>
Develops, supports, and/or leads quality improvement initiatives; develops approaches to linking quality improvement to outcomes reported through dashboard or key indicator data or surveys and observation studies</p></li><li><p>
Works with institutional leadership to develop improvement efforts</p></li><li><p>
Reviews documentation and assesses effectiveness of documentation review approaches; analyses causes and develops solutions for documentation failures</p></li><li><p>
Gathers data and/or develops research and data analysis projects</p></li><li><p>
Develops and carries out complex audits requiring content and operational knowledge of activity being audited</p></li><li><p>
Maintains employee records of training and credentialing as required by unit activity assigned and associated regulatory standards</p></li><li><p>
Can perform audits to ensure compliance against standards, regulations, procedures, policies, IND/IDE and clinical trials</p></li><li><p>
Perform trending and analyzing of data using appropriate quality and statistical tools. Assist in reporting data within and external to the department, institution, across institutions, and to governmental agencies</p></li><li><p>
Assist / develop training documentation, review/audit competency assessments and training documentation to ensure that employee record corresponds with tasks employee is performing</p></li><li><p>
CAPA &ndash; Assist with correction and preventative action plans based on audit findings, deviations and events. Plan follow up audits to assess if the desired effect / change was achieved</p></li></ul><p><b>
KNOWLEDGE, SKILLS, AND ABILITIES REQUIRED:</b></p><ul><li><p>
Maintain basic knowledge of applicable standards and regulations to ensure department / institution ongoing compliance with accreditation standards (FACT, JC) and inspection regulations (FDA, DPH,CMS, DOT)</p></li><li><p>
Outcome analysis - Review / interpret / report relevant information as assigned or to present to physician or other investigator</p></li><li><p>
Subject matter expertise &ndash; provide assistance in a given area of expertise (microbiology, immunohematology, cell processing, informatics, clinical operations etc) to help the department / program achieve its stated objectives and goals for the overall improvement of the program</p></li><li><p>
Strong Excel skills required.</p></li></ul><p></p><p><b><br>
MINIMUM JOB QUALIFICATIONS:</b></p><p>
The position requires a BS/BA degree in science, medical technology, or a related field. Candidates must have at least 5 years of experience in a relevant field, such as clinical laboratories, blood banks, clinical settings, or the biologic/pharma industry.</p><p><b>
SUPERVISORY RESPONSIBILITIES:
</b></p><p>Provides training and support to relevant staff (CMCF, KFBDC, Clinicians, etc) in areas of expertise. No direct reports.</p><p><b>
PATIENT CONTACT:
</b></p><p>Limited contact with patients, donors and families, but extensive review of patient&rsquo;s / donor&rsquo;s medical records (adults and pediatrics).</p><p>
At Dana-Farber Cancer Institute, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. As relentless as we are in our mission to reduce the burden of cancer for all, we are committed to having faculty and staff who offer multifaceted experiences. Cancer knows no boundaries and when it comes to hiring the most dedicated and compassionate professionals, neither do we. If working in this kind of organization inspires you, we encourage you to .</p><p>
Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law.
</p><h3 class="jobSectionHeader"><b>EEO Poster</b></h3>
.<p>
Pay Transparency Statement</p><p>
The hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate&rsquo;s relevant experience, skills and qualifications.</p><p>
For union positions, the pay range is determined by the Collective Bargaining Agreement (CBA).</p>
$76,900.00 - $86,100.00</div></div></div><p></p>

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