compliance reviewer

Intertek

<div></div><div><p><b>Label Reviewer</b></p><p>
Intertek, helping companies around the world develop products to be used safely by millions of people every day, is searching for reliable candidates with a strong attention to detail to join a new project team dedicated to reviewing product labels for a large retailer. These positions will be part of Intertek&rsquo;s Assuris team, and is a fantastic opportunity to begin a quality assurance career in retail consumer goods.</p><p><i>
Intertek Assuris is an unparalleled team of industry-leading experts providing science-based assurance in quality, safety, and sustainability. Our global network of scientists, engineers, and regulatory specialists provides support to navigate complex scientific, regulatory, environmental, health, safety, and quality challenges throughout the value chain. Through our regulatory, scientific and industry insights, we empower companies with solutions designed to enable market access, assess and mitigate risk, preserve and promote human health, and protect the environment.</i></p><p><b>
What are we looking for?</b></p><p>
The <b>Label Reviewer </b>position is responsible for reviewing product labels and documentation against regulatory, quality, and internal standards. Documentation of these findings is highly detailed, and familiarity with MS Office products is a plus. The role requires accuracy, process discipline, and comfort working in a high-volume, deadline-driven environment. Employees will have some flexibility with scheduling requirements, but may be required to work weekends and Holidays from time-to-time.<br>
<br>
This position is fully remote. However, we are prioritizing candidates located near Bentonville, AR, who may be available for occasional onsite visits.</p><p><b>
Job Title:</b> <b>Label Reviewer, Part-time or Full-time</b></p><p><b>
Location: Remote</b></p><p><b>
Salary &amp; Benefits Information</b></p><p><b>
The base wage or salary range for this position is $23</b><b> - $26 per hour</b><b>. Individual compensation packages are based on a variety of factors unique to each candidate including skill set, experience, qualifications, and other job-related reasons.</b></p><p>
In addition to competitive compensation packages, when working with Intertek you can expect benefits including medical, dental, vision, life, disability, 401(k) with company match, generous vacation / sick time (PTO), tuition reimbursement and more for full-time positions.</p><p><b>
What you&rsquo;ll do:</b></p><p>
The <b>Label Reviewer</b> position is responsible for the following duties:</p><ul><li>
Review labels, documents, and records against checklists, SOPs, and regulatory standards.</li><li>
Identify discrepancies, formatting errors, or missing substantiation, and document findings clearly.</li><li>
Maintain accurate, audit-ready records of reviews and corrections.</li><li>
Meet daily/weekly throughput quotas while sustaining accuracy.</li><li>
Log and track work in spreadsheets, databases, and workflow dashboards.</li><li>
Escalate unclear, ambiguous, or high-risk issues to senior reviewers or experts.</li><li>
Collaborate cross-functionally with other review teams (Formatting, Ingredient, Claims, QA/QC).</li><li>
Communicate findings and updates clearly through email, messaging, and shared systems.</li><li>
Work independently and effectively in a remote, process-driven environment.</li></ul><p>
This position outline is a general guideline and does not represent all encompassing details. The position assumes that the incumbent has both the mental and physical requirements to carry out the above defined duties.
</p><p><b>What it takes to be successful in this role:</b></p><ul><li>
High School Diploma or equivalent</li><li>
1+ years of hands-on experience thriving in a fast-moving, deadline-focused role.</li><li>
1+ years of working on a computer with technical or tedious workload</li><li>
Strong level of comfort with Microsoft Office products (Excel, Word, Outlook)</li><li>
Strong attention to detail and accuracy across repetitive tasks.</li><li>
Ability to interpret structured guidance and apply rules consistently.</li><li>
Proficiency with spreadsheets, databases, and workflow/task management tools.</li><li>
Excellent written communication and documentation skills.</li><li>
Reliable, self-directed, and able to meet deadlines in a remote environment.</li><li>
Comfortable handling confidential or sensitive product information.</li><li>
This is a remote position; however, applicants must reside in and be able to legally work in the United States.</li></ul><p><b>
Preferred Requirements &amp; Qualifications:</b></p><ul><li>
Completed an Associate&rsquo;s degree program, or higher</li><li>
2+ years of experience in a time-sensitive, high-paced professional setting, such as an office</li><li>
Experience with QC/QA work</li><li>
Experience in regulatory compliance, document review, quality assurance, or related fields</li><li>
Availability to work weekend and Holiday hours is a plus.</li></ul><p></p><p><b><br>
Intertek: Total Quality. Assured.</b></p><p>
Intertek is a world leader in the Quality Assurance market, with a proven, high-quality business model and a global network of customer-focused operations and highly engaged subject matter experts. With passion, pace, and precision we work to exceed our customers&rsquo; expectations, while engaging with our employees to be 10X in their performance and professional growth.</p><p>
Intertek is a drug-free workplace. As a condition of employment, certain positions may be required to pass a pre-employment drug test based on the type of work that will be performed.</p><p>
For individuals with disabilities who would like to request accommodation, or who need assistance applying, please email hr.eeo@intertek.com or call 1-877-694-8543 (option #5) to speak with a member of the HR Department.</p><p><b>
Our Culture of Total Quality Assurance</b></p><p>
Intertek promotes a culture where motivated, customer-oriented employees can flourish, experience professional fulfillment, and reach their highest potential. At Intertek, we exercise our spirit of innovation, the passion of our people and our unmatched customer commitment to realize our purpose of making the world an ever better, safer, and more sustainable place for all.</p><p>
A career with Intertek offers rewarding opportunities to help companies around the world develop products to be used safely by millions of people every day. Intertek is the trusted advisor to many of the world&rsquo;s leading brands, companies, and governments, and has earned a reputation for accuracy, reliability, integrity, and technical competence. Working at Intertek means joining a global network of state-of-the-art facilities and passionate people who deliver superior customer service with a purpose of bringing quality, safety, and sustainability to life.</p><p><b>
We Value Diversity</b></p><p>
Intertek&rsquo;s network of phenomenal people are our greatest assets, and the diversity they bring fuels our success. Intertek is an Equal Employment Opportunity Employer that values inclusion and diversity. We take affirmative action to ensure all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other legally protected characteristics.</p><p></p><p><br>
#LI-DR</p><ul><li><i>Intertek does not accept unsolicited approaches from agencies and will not pay a fee for any placement resulting from the receipt of an unsolicited resume.</i></li></ul>
Intertek&rsquo;s Health, Environmental &amp; Regulatory Services (HERS) business line is renowned for its high-quality solutions delivered through its global network of world-class scientific, engineering, toxicological and regulatory experts. Additionally, HERS provides regulatory compliance support, as well as industry-agnostic solutions pertaining to sustainability, quality, and safety, empowering companies to mitigate risks and make informed decisions relating to their products and processes.Intertek is a leading Total Quality Assurance provider to industries worldwide. Our network of more than 1,000 laboratories and offices in more than 100 countries, delivers innovative and bespoke Assurance, Testing, Inspection and Certification (ATIC) solutions for our customers' operations and supply chains. Working at Intertek means joining a global network of state-of-the-art facilities and passionate people who deliver superior customer service with a purpose of bringing quality, safety, and sustainability to life.</div>

Label Reviewer

Adstra

<div>Overview:
<p><b><i>
At Adstra we know great things happen when people come together with one shared goal. The future of data is happening at Adstra. Come join our growing team.</i></b></p><div></div><p><br>
We are currently seeking a <b>Marketing Compliance QA Specialist </b>to join our team of professionals.</p><p></p><p><b><br>
You will be responsible </b>for the review and validation of team members&rsquo; completed marketing submissions ensuring compliance of legal, regulatory, and branding guidelines; maintaining checklists and documentation within systems; and supporting other internal audit/quality assurance projects, reporting, and training as requested by leadership.</p><p></p><p><b><br>
Our &ldquo;ideal candidate&rdquo; </b>must have a minimum of 12 months experience conducting &quot;live reviews&quot; in a Compliance Review role at Adstra and has consistently recieved very strong QA ratings<b>. </b>In addition, our &quot;ideal candidate&quot; is an individual who has experience in compliance, quality assurance, marketing; has experience with creative asset review for direct marketing promotions; and has a proven ability for attention to detail, interpreting guidelines, making decisions and effectively meeting deadlines.</p>
Responsibilities:
<div><i>
Responsibilities for this opportunity include, but are not limited to</i>:</div><ul><li>
Conduct and deliver timely Quality Assurance audits and effectively communicate results and required actions to the team;</li><li>
Document and report all Quality Assurance testing results;</li><li>
Communicate effectively with cross-functional teams and stakeholders;</li><li>
Deliver training and guidance based on QA findings;</li><li>
Manage and prioritize projects to meet established deadlines;</li><li>
Interpret client&rsquo;s business guidelines and policies to ensure compliance with legal and company guidelines and processes;</li><li>
Lead projects and initiate solutions and process improvements and key initiatives to completion.</li></ul>
Qualifications:
<div><i>
In addition, our &quot;ideal candidate&quot; has the following skills &amp; experience:</i></div><ul><li>
Must have a minimum of 12 months experience conducting &quot;live reviews&quot; in a Compliance Review role at Adstra and has consistently recieved very strong QA ratings</li><li>
College Degree from an accredited college or university (Business, Marketing preferred) or 5-7 years of professional experience in lieu of college degree required;</li><li>
Must have experience as a QA reviewer with a very strong QA rating for a minimum of 12 months at Adstra;</li><li>
4+ years in compliance and creative content quality reviews;</li><li>
Strong attention to detail and proofreading skills. Ability to deliver high-level quality work;</li><li>
Interpretation of information and decision-making skills to make judgements and determine if guidelines apply;</li><li>
Strong communication skills;</li><li>
Strong team player who has proven success collaborating effectively with others;</li><li>
Organized self-starter with the ability to multitask and prioritize projects in a deadline intensive environment.</li></ul><div></div><p><b><br>
About Adstra</b></p><div><b>
Adstra</b>, a privately held, PE backed company, provides a comprehensive and unique suite of identity, data, and audience solutions to a diverse base of blue-chip clients.</div><div><br>
</div><div><b>Adstra</b> delivers the new model for data-driven enterprises. Based on a culture of innovation, quality, and inclusion, <b>Adstra</b> offers a comprehensive suite of transparent, compliant, and cross media solutions. <b>Adstra&rsquo;s</b> goal is to liberate brands from legacy marketing technology and data approaches to maximum value and efficiency from their data and customer touchpoints.</div><div><br>
</div><div><b>Adstra</b> works across industry verticals, both for profit and nonprofit, as a leading provider of identity resolution, customer acquisition, consumer data, data management, and marketing execution services. <b>Adstra</b> is headquartered in Princeton, New Jersey with associates working across the United States.</div><div></div><div><b><br>
Adstra</b> offers excellent benefits including medical, dental, vision, life, LTD, 401k w/ company match, paid time off, business casual dress, summer hours, customized training &amp; more! If you are one of the &ldquo;best and brightest&rdquo; in your field and you&rsquo;re looking to position yourself for the future, this is a great opportunity.</div><div><br>
</div><div><i>To learn more about why </i><b><i>Adstra</i></b><i> is the new ideal in places to work check out our </i><b><i>Adstra Careers</i></b><i> page today!</i></div><div></div><p><b><br>
Equal Employment Opportunity</b></p><p><b>
Adstra</b> provides equal employment opportunities to all employees and applicants for employment. All practices such as recruitment, selection, promotions, and other terms and conditions of employment are administered in a manner that ensures there is no discrimination on the basis of race, color, national origin, ancestry, religion, citizenship, age, gender, gender expression or identity, sexual orientation, marital status, disability, pregnancy, medical condition, genetic information, protected veterans, or any other protected characteristic under applicable law.</p><p>
For immediate consideration, please create a profile and make sure you provide your resume and current contact information. We look forward to learning more about you and the value you can bring to <b>Adstra!</b></p><p></p><p><b><i><br>
We want to be your Employer of Choice!</i></b></p><p><br>
</p><p><b>EOE/M/F/D/V</b></p></div><div></div>

Marketing Compliance QA Specialist

Staffing Solutions Organization LLC (SSO)

Staffing Solutions Organization LLC (SSO), an affiliate of Public Consulting Group LLC (PCG), is focused on delighting clients with world-class managed staffing and talent consulting services. SSO is committed to a diverse workforce, which is a reflection of our clients and the people they serve.
<br><br>
Nurse Reviewer – Illinois
<br><b>Location:</b> Remote with on site visits across Illinois
<br><br>
Position Overview
<br>The Nurse Reviewer conducts provider compliance reviews to ensure adherence to state regulations, quality standards, and program requirements. This role includes conducting onsite visits, evaluating documentation, and determining provider compliance. The Nurse Reviewer works independently, exercises sound judgment, and provides recommendations that guide provider improvement and support statewide oversight efforts.
<br><br>
Duties & Responsibilities
<br><ul>
<li>Build and maintain effective relationships with providers and users to support high quality customer service.</li>
<li>Evaluate providers for compliance with applicable state and program regulations.</li>
<li>Coordinate and schedule on site provider visits; clearly communicate visit requirements.</li>
<li>Conduct compliance interviews with providers and gather all necessary information.</li>
<li>Review provider documentation, policies, and business practices for regulatory alignment.</li>
<li>Collect, organize, and submit documentation supporting compliance findings.</li>
<li>Utilize technology and web based systems to convert paper documentation to electronic format.</li>
<li>Conduct in person assessments of provider sites to evaluate compliance with oversight requirements.</li>
<li>Summarize on site visit findings accurately and professionally.</li>
<li>Exercise independent judgment to evaluate compliance and make final determinations based on documented evidence.</li>
<li>Identify deficiencies and recommend appropriate next steps to support provider improvement.</li>
<li>Analyze trends in non compliance and identify gaps in provider business processes.</li>
<li>Provide timely recommendations and updates to the Supervisor.</li>
<li>Maintain HIPAA standards and confidentiality at all times.</li>
<li>Perform other duties as assigned.</li>
</ul>
Required Skills
<br><ul>
<li>Strong interpersonal skills with the ability to relate well to staff and providers.</li>
<li>Active listening and effective communication skills.</li>
<li>Proficiency in MS Word, Excel, Outlook, and web based applications.</li>
<li>Process oriented and results driven work approach.</li>
<li>Ability to foster teamwork and collaborate across levels of management and staff.</li>
<li>Ability to work independently and within a team environment.</li>
<li>Excellent written and verbal communication skills and customer service techniques.</li>
<li>High accuracy, strong attention to detail, and commitment to quality.</li>
<li>Proven ability to meet deadlines and follow strict standards.</li>
<li>Ability to travel regularly to provider sites across Illinois.</li>
</ul>
Qualifications
<br>Education
<br><ul>
<li>Bachelor’s degree in any field (Nursing preferred)</li>
</ul>
Experience
<br><ul>
<li>Minimum 2 years of clinical experience working with critical care providers, public health providers, or providers serving children, older adults, individuals with traumatic brain injury, or individuals with developmental disabilities.</li>
<li>Minimum 1 year of experience conducting quality assurance reviews.</li>
</ul>
Certification
<br><ul>
<li>Active Illinois Registered Professional Nurse (RN) license required.</li>
</ul>
Working Conditions
<br><ul>
<li>Remote work with 2–3 on site provider visits per week throughout the state of Illinois.</li>
</ul>
Benefits (Through SSO)
<br>SSO offers a competitive benefits package that supports your health, financial well being, and long term growth, including:
<br><ul>
<li>Medical, dental, and vision insurance</li>
<li>401(k) with discretionary employer match</li>
<li>Paid time off and holidays</li>
<li>Flexible spending accounts</li>
<li>Additional employee perks</li>
</ul>
Keyword Search Terms
<br>Nurse Reviewer, RN Reviewer, Provider Management Specialist, Compliance Nurse, Healthcare Quality Review, Provider Compliance, Medicaid Compliance, Clinical Reviewer, Illinois RN, Site Visit Nurse, Healthcare Auditor, Public Health Nursing, QA Nurse, Provider Monitoring.
<br><br>
Compensation for roles at Staffing Solutions Organization LLC (SSO) varies depending on a wide array of factors including, but not limited to, the specific office location, role, skill set, and level of experience. As required by applicable law, SSO provides a reasonable range of compensation for this role. In addition, SSO provides a range of benefits for this role.
<br><br>
Applicants must be authorized to work in the U.S. This position is not eligible for work authorization sponsorship (including H-1B sponsorship) by SSO and under the federal laws relating to the F-1 STEM EAD program, this position is not eligible to support a STEM EAD extension application.
<br><br>
All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, gender identity, marital status, age, national origin, protected veteran status, or disability. Staffing Solutions Organization LLC is an E-Verify participant.

Nurse Reviewer

Otsuka ICU Medical LLC

<div><p><b>Responsibilities
</b></p><p>Conduct investigations into process excursions, procedural exceptions and nonconforming events that contribute to the root cause of customer complaints. Ensure root cause, corrective action preventative action (CAPA), and product impact are thoroughly addressed in investigations. Synthesize recommendations for action based on procedural requirements, decision flowcharts, and critical thinking. Document investigations results. Develop, implement, manage and track effectiveness of corrective action plans for exceptions. Provide training and conduct verification assessments to ensure adequate maintenance of quality systems and processes as required. Manage projects to ensure they are completed within the required time schedule as required per quality systems. Provide support activity during regulatory or 3rd party audits. Prepare departmental metrics. Utilize trend data to develop schedule and incorporate into facility investigations. Ensure accurate project schedules are maintained and communicated to management. Write field alert report and prepare and deliver notifications to management. Participate on committees/teams supporting GMP compliance programs. Adhere to all company guidelines, SOPs and ensure required compliance training is up to date. Monitor GMP and regulatory compliance activities critical in a regulatory inspection. Communicate GMP violations and quality systems deficiencies to management and recommend MQ product release holds until the violation is addressed. Perform other related duties as assigned or required. *Work from home permitted. When not working from home, must report to Austin, TX office. *&lt; 5% domestic travel required per year.
</p><p><b>EDUCATION AND EXPERIENCE REQUIREMENTS:
</b></p><p>Bachelor&rsquo;s degree (or foreign equivalent) in Industrial Engineering, Manufacturing Engineering, or closely related field plus two (2) years of experience in Quality, Manufacturing, Engineering, R&amp;D Functions, job offered, or closely related occupation.
</p><p><b>SPECIAL REQUIREMENTS:
</b></p><p>Must possess expertise/knowledge sufficient to adequately perform the duties of the job being offered. Expertise/knowledge may be gained through employment experience or education. Such expertise/knowledge cannot be &ldquo;quantified&rdquo; by &ldquo;time.&rdquo; Required expertise/knowledge includes: Experience with Manufacturing principles including one or more of the following: Good Manufacturing Practices (GMP), Technical writing, and Quality Management System (QMS) business process experience; Experience with problem solving using Root Cause Analysis tools; Experience with regulatory requirements including 21 CFR part 11, 210 &amp; 211; Experience effectively communicating with all levels of management through writing and/or presentation; Experience recommending continuous improvement plans where necessary using the Six Sigma and/or DMAIC methodologies; Experience fostering a participative approach to problem-solving by conducting cross-functional team meetings and presenting significant events to leadership for input; Experience with corrective action follow up utilizing technical expertise and negotiation skills to bridge the gaps between Quality and Manufacturing requirements.
</p><p>Otsuka ICU Medical, LLC is an equal opportunity employer.
</p><p>To apply for Otsuka ICU Medical, LLC&rsquo;s Compliance Investigator position please send resume to: humanresouces&amp;#64;icumed.com
</p><p>Must reference <b>JOB CODE: </b>TX1224HA</p></div><p></p>
<br><p></p><div><p>Innovation, Impact, and Purpose.
</p><p>Find Your Future Here.
</p><p>We manufacture the critical IV solutions providers count on to deliver consistent, reliable care. Each product we make helps ensure patients receive the therapies they need without disruption.
</p><p>When you work here, you become part of something bigger&mdash;a team dedicated to reliability and innovation. No matter the role, your work directly strengthens the healthcare supply chain and impacts patients nationwide.
</p><p>We offer opportunities for growth, collaboration, and meaningful contributions, all in pursuit of a mission that truly matters.
</p><p>Join us and help shape the future of IV solutions.
</p><p>EEO Statement:
</p><p>Otsuka ICU Medical is committed to being an Equal Opportunity Employer. We ensure that all qualified applicants receive fair consideration for employment regardless of race, color, nationality or national origin, ethnicity, sex, gender, religion or belief, marital or civil partnership status, sexual orientation, pregnancy or maternity, age, disability, or protected veteran status.
</p><p>If you are an individual with a disability and need reasonable accommodation to participate in the employment selection process, please contact us at austinhr@icumed.com. We are committed to providing equal access and opportunities for all candidates.
</p><div><p>Otsuka ICU Medical EEO Policy Statement
</p><p>Know Your Rights: Workplace Discrimination is Illegal Poster
</p><p>Otsuka ICU Medical CCPA Notice to Job Applicants</p></div></div>

Compliance Investigator

AllMed Healthcare Management, Inc

<div><div><div><b>AllMed </b>is looking for a dedicated <b>Pharmacy Technician</b> to join our growing team! This is your chance to work in a dynamic, supportive environment where your skills and attention to detail help improve lives every day.</div></div><div><div>
The Pharmacy Technician is responsible to ensure reports are of the highest quality and integrity and in full compliance with client contractual agreement, regulatory agency standards and/or federal and state mandates.</div></div><div><div>
This position is <b>100% remote</b> and full time.
</div></div><div><div><b>Responsibilities may include:</b></div></div><ul><li><div><div>
Performs quality assurance review of reports, correspondences, addendums or supplemental reviews.</div></div></li><li><div><div>
Ensures clear, concise, evidence-based rationales have been provided in support of all recommendations and/or determinations.</div></div></li><li><div><div>
Ensures that all client instructions and specifications have been followed and that all questions have been addressed.</div></div></li><li><div><div>
Ensures each review is supported by clinical citations and references when applicable and verifies that all references cited are current and obtained from reputable medical journals and/or publications.</div></div></li><li><div><div>
Ensures the content, format, and professional appearance of the reports are of the highest quality and in compliance with company standards.</div></div></li><li><div><div>
Ensure that the appropriate board specialty has reviewed the case in compliance with client specifications and/or state mandates and is documented accurately on the case report.</div></div></li><li><div><div>
Verifies that the peer reviewer has attested to only the fact(s) and that no evidence of reviewer conflict of interest exists.</div></div></li><li><div><div>
Ensures the provider credentials and signature are adhered to the final report.</div></div></li><li><div><div>
Identifies any inconsistencies within the report and contacts the Peer Reviewer to obtain clarification, modification or correction as needed.</div></div></li><li><div><div>
Assists in resolution of customer complaints and quality assurance issues as needed.</div></div></li><li><div><div>
Ensures all federal ERISA and/or state mandates are adhered to at all times.</div></div></li><li><div><div>
Provides insight and direction to management on consultant quality, availability and compliance with all company policies and procedures and client specifications.</div></div></li><li><div><div>
Promotes effective and efficient utilization of company resources.</div></div></li><li><div><div>
Participates in various educational and or training activities as required.</div></div></li><li><div><div>
Performs other duties as assigned.</div></div></li></ul><div><div>
If you're ready to take the next step in your pharmacy career, we&rsquo;d love to hear from you!</div></div><ul><li><div><b>
A minimum of two years of working as a pharmacy tech or clinical/related field experience equivalent combination of education and experience.</b></div></li><li><div>
High school diploma or equivalent required.
</div></li><li><div>Active Pharmacy Tech License/ Certificate
</div></li><li><div>Must have strong knowledge of medical terminology, anatomy and physiology, medications and laboratory values.</div></li><li><div>
Must be able to add, subtract, multiply, and divide in all units of measure, using whole numbers and decimals; Ability to compute rates and percentages.</div></li><li><div>
Must be a qualified typist with a minimum of 40 W.P.M</div></li><li><div>
Must be knowledgeable of multiple software programs, including but not limited to Microsoft Word, Outlook, Excel, and the Internet.</div></li><li><div>
Must possess excellent skills in English usage, grammar, punctuation and style.</div></li><li><div>
Ability to accurately follow instructions and respond to directions from upper management.</div></li><li><div>
Demonstrates accuracy and thoroughness. Looks for ways to improve and promote quality and monitors own work to ensure quality is met.</div></li><li><div>
Must demonstrate exceptional communication skills by conveying necessary information accurately, listening effectively and asking questions where clarification is needed.</div></li><li><div>
Must be able to work independently, prioritize work activities and use time efficiently.</div></li><li><div>
Must be able to maintain confidentiality.</div></li><li><div>
Must be able to demonstrate and promote a positive team-oriented environment.</div></li></ul><div><div>
AllMed provides clinical decision making and utilization management solutions to leading payer and provider organizations. We work closely with your team toward a shared vision of healthcare that delivers the highest quality, values patient experience, and ensures both appropriate care and utilization of health-related services.</div></div><p>
</p><div><div><b>AllMed </b>offers a fast-paced team atmosphere with competitive benefits (medical, vision, dental), paid time off, and 401k.</div></div><p>
</p><div><div>Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected category under applicable federal, state, and local laws.</div></div></div>

Pharmacy Technician

Maryland Department of Transportation

<p></p><div><div><div><div><b>(Open Recruitment)</b></div><div><b>
State Highway Administration</b></div><div><b>
Access Management Project Reviewer (Transportation Engineer IV)</b></div><div><b>
 Grade 18 (0516) SP# 26-84-04</b></div><div><b><br>
 YOU MUST APPLY ONLINE TO BE CONSIDERED FOR THIS POSITION</b></div><div><b>
http://www.governmentjobs.com/careers/mdotmd</b></div><div></div><div><br>
The State Highway Administration's (SHA) <b>District 4 (Baltimore County)</b> is currently recruiting for an <b>Access Management Project Reviewer (Transportation Engineer IV) </b>position. This position is <b>open to anyone who meets the minimum qualifications </b>listed below. The resulting list of eligible candidates will be used to fill this vacancy and may be used to fill future vacancies in this classification.</div><div><br>
<b>Nature of Work</b><b>: </b>The primary purpose of this position is to represent State Highway Administration (SHA) in District 4 as a Project Reviewer in the Access Management Section through interface and coordination with federal, state, county, and municipal agencies as well as citizens, developers, and consulting engineers. This position works directly for the Regional Engineer and assists the Regional Engineer in the review of development project documents, preparation of comments related to the district, and, under the supervision of the Regional Engineer, negotiates the application of requirements for access and highway related improvements, providing technical direction and consultant engineer coordination of SHA requirements. The primary purpose of this position is to enforce the regulations stipulated in the Annotated Code of Maryland. The Project Reviewer has the authority to recommend to the Regional Engineer that immediate corrective action is necessary. Under the direction of the Regional Engineer, the Project Reviewer will coordinate as necessary with appropriate parties to withhold the issuance of a SHA approval of a development submission and/or the access permit in the review of subdivision plans, site development plans, grading plans, and building permits through the County Review and SHA development review processes for all assigned projects.</div><div></div><i><br>
MDOT offers a generous and competitive benefits package. You can learn about our amazing benefits here</i><b><i>: </i></b><b><i>MDOT Benefits Guide</i></b><br>
<br>
<i>&ldquo;The State Highway Administration (SHA) has been named a Training magazine Training Awards winner for the seventh consecutive year.&quot;</i></div><p></p>
<div><h2 class="jobSectionHeader"><b>Qualifications</b></h2></div>
<p></p><div><p><b>MINIMUM QUALIFICATIONS:</b></p><p><b>
Education</b>: Possession of a bachelor's degree in engineering from an accredited college or university.<br>
<br>
<b>Experience</b>: Four (4) years of experience in professional engineering.</p><div><b>
Selective Qualification: </b>Two (2) years of the required experience must have involved traffic engineering, highway design, land development, access management, or<b> </b>construction project engineer experience.<br>
<br>
<ul><li><b>This statement contains a selective qualification, which is more focused in scope than the minimum qualifications for this classification. Selective qualifications are utilized when the position requires specific or additional bona fide occupational qualifications (i.e., knowledge, skill or ability).</b></li></ul></div><p><b>
Preferred Qualifications:</b></p><p><i>
The ideal candidate should possess the following:</i></p><div><ul><li>
Ability to negotiate with parties outside of state government; facilitate agreements between parties that have differences between them.</li><li>
Good computer skills and knowledge of Microsoft Office programs (e.g., Word, Excel, Access and PowerPoint) are desirable.</li><li>
Working knowledge of AASHTO (American Association of State Highway and Transportation Officials) guidelines.</li><li>
Working knowledge of Standards and Specifications for Highway Design and Construction.</li><li>
Working knowledge of Traffic Engineering principles.</li><li>
Excellent written and oral communication skills.</li><li>
Knowledge in preparing technical reports.</li><li>
Possession of an Engineer-in-Training License from the Maryland Department of Labor, Licensing, and Regulation</li></ul></div><div><br>
<b>Notes:</b><br>
<br>
1. Additional work experience in professional engineering, or in technical engineering at the journey level or above, may be substituted on a year for year basis for the required education.<br>
<br>
2. Possession of a master's degree in engineering may be substituted for one year of the required experience.</div><br>
<div></div>
3. Persons currently registered as Professional Engineers in the State of Maryland, or in a state with comparable requirements, are considered to have met the education requirements.</div><p></p>
<div><h2 class="jobSectionHeader"><b>Licenses &amp; Certifications</b></h2></div>
<p></p><div><div>Candidate must possess a motor vehicle operator's license valid in the state of Maryland.</div></div></div></div><p></p>

Access Management Project Reviewer (Transportation Engineer IV)

MES Solutions

<div><div><div><b>Ready for a Rewarding Career that Fits Your Lifestyle?</b>
</div></div><p></p><div><div>Imagine a job where you can keep your <b>clinical skills sharp</b>, tackle exciting challenges, AND work from the comfort of your own home. Sounds like the perfect mix, right?</div></div><p>
</p><p></p><div><div><b>MES</b> is looking for a <b>self-driven, high-performing Registered Nurse (RN)</b> to join our dynamic team as a <b>Clinical Quality Assurance Coordinator</b>. In this role, you&rsquo;ll ensure our <b>Peer Review case reports</b> are nothing short of exceptional&mdash;delivering top-notch quality and integrity, all while staying fully aligned with <b>client agreements</b>, <b>regulatory standards</b>, and <b>state and federal mandates</b>.</div></div><p>
</p><div><div>The position is <b>100% remote</b> with a schedule of<b> </b><b>Monday through Friday:
</b></div></div><ul><li><div>3 days: 12 - 8:30pm EST</div></li><li><div>
2 days: 8 - 4:30pm/ 9 - 5:30pm EST (flexible)</div></li></ul><p>
</p><ul><li><div>Performs quality assurance review of peer review reports, correspondences, addendums or supplemental reviews.</div></li><li><div>
Ensures clear, concise, evidence-based rationales have been provided in support of all recommendations and/or determinations.</div></li><li><div>
Ensures that all client instructions and specifications have been followed and that all questions have been addressed.</div></li><li><div>
Ensures each review is supported by clinical citations and references when applicable and verifies that all references cited are current and obtained from reputable medical journals and/or publications.</div></li><li><div>
Ensures the content, format, and professional appearance of the reports are of the highest quality and in compliance with company standards.</div></li><li><div>
Ensure that the appropriate board specialty has reviewed the case in compliance with client specifications and/or state mandates and is documented accurately on the case report.</div></li><li><div>
Verifies that the peer reviewer has attested to only the fact(s) and that no evidence of reviewer conflict of interest exists.</div></li><li><div>
Ensures the provider credentials and signature are adhered to the final report.</div></li><li><div>
Identifies any inconsistencies within the report and contacts the Peer Reviewer to obtain clarification, modification or correction as needed.</div></li><li><div>
Assists in resolution of customer complaints and quality assurance issues as needed.</div></li><li><div>
Ensures all federal ERISA and/or state mandates are adhered to at all times.</div></li><li><div>
Provides insight and direction to management on consultant quality, availability and compliance with all company policies and procedures and client specifications.</div></li><li><div>
Promote effective and efficient utilization of company resources.</div></li><li><div>
Participate in various educational and or training activities as required.</div></li><li><div>
Perform other duties as assigned.</div></li></ul><p>
</p><div></div><div><div>If you&rsquo;re ready to make a real impact in healthcare, all while enjoying the flexibility of working remotely, we want to hear from you!
</div></div><p></p><ul><li><div>Active RN nursing license required.</div></li><li><div>
Must be a graduate of an accredited nursing program or related medical experience; bachelor's degree preferred.</div></li><li><div>
A minimum of two years clinical or related field experience; or equivalent combination of education and experience.
</div></li><li><div>Must have strong knowledge of medical terminology, anatomy and physiology, medications and laboratory values.</div></li><li><div>
Must be able to add, subtract, multiply, and divide in all units of measure, using whole numbers and decimals; Ability to compute rates and percentages.</div></li><li><div>
Must be a qualified typist with a minimum of 40 W.P.M</div></li><li><div>
Must be able to operate a general computer, fax, copier, scanner, and telephone.</div></li><li><div>
Must be knowledgeable of multiple software programs, including but not limited to Microsoft Word, Outlook, Excel, and the Internet.</div></li><li><div>
Must possess excellent skills in English usage, grammar, punctuation and style.</div></li><li><div>
Ability to follow instructions and respond to upper managements&rsquo; directions accurately.</div></li><li><div>
Demonstrates accuracy and thoroughness. Looks for ways to improve and promote quality and monitors own work to ensure quality is met.</div></li><li><div>
Must demonstrate exceptional communication skills by conveying necessary information accurately, listening effectively and asking questions where clarification is needed.</div></li><li><div>
Must be able to work independently, prioritize work activities and use time efficiently.</div></li><li><div>
Must be able to maintain confidentiality.</div></li></ul><p>
</p><p></p><div><div><b>MES Solutions</b> is a premier provider of independent medical examination and peer review services to the insurance, corporate, legal, and government sectors. Members of our credentialed medical panel conduct physical examinations or medical record reviews, delivering reports that assist clients in the resolution of automotive, disability, liability, and workers' compensation claims. MES has been providing services nationally since 1978 in accordance with the industry's highest standards of operating excellence and regulatory compliance.</div></div><p>
</p><p></p><div><div>Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected category under applicable federal, state, and local laws.</div></div><div><div><b>
Equal Opportunity Employer - Minorities/Females/Disabled/Veterans</b></div></div><div><div><b><i>
MES offers a fast-paced team atmosphere with competitive benefits (medical, vision, dental), paid time off, and 401k.</i></b></div></div></div>

Clinical Quality Assurance Coordinator

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