Role Description IEM is looking for a Full Time - Verification of Benefits and Quality Control Specialist (VOB QC Specialist) who will be responsible for reviewing applications for quality, comprehensiveness, and eligibility while documenting and communicating with case managers as needed within the functional area with limited supervision. A VOB/QC Specialist will maintain a complete understanding of all applicable program policies, procedures, and requirements within the guidelines established to follow program compliance. May also provide support with day-to-day project management activities for quality control, which may include supplementary responsibilities relative to the program and its needs. Primary Location: Live anywhere that meets personal office/home work requirements in the United States including Puerto Rico. Preference will be given to candidates who reside in Pasco County, Florida. Work will take place either in an office environment, or from a personal location and will depend on the need of the project. - Review records for duplication of benefits (DOB), fraud, waste, inconsistencies, investigate, and collaborate with internal partners to resolve issues with analysis and customer service skills. - Log support issues, communicate, resolve and escalate according to defined standard operating procedures. - Analyze and verify documentation provided for inconsistencies, accuracy, and various discrepancies with an understanding of program policy. - Understand program needs, policy, departmental process flows, and standard operating procedures. - Participate in updates and improvements to Verification of Benefits & Quality Control policies and processes. - Follow-up with identified compliance issues, initiate corrective actions, based on policy guidelines, and implement program controls, as necessary. - Manage individual workload, productivity, and communications that enable accurate, efficient, and policy compliant processing. - Contribute to team success with effective communication and sound decision making. - Respond to questions and requests professionally and in a timely manner. Qualifications - An Associate’s degree from an accredited university in a Business, Business Administration, Finance or Accounting, Communications, Public Administration / Policy, or relevant field. - Three (3) or more years of experience providing high level review of documentation and strong analytical skills. - An equivalent combination of experience and training that demonstrates the required knowledge, skills, and abilities necessary to effectively perform the duties and functions of this position may be considered in lieu of a degree. - Ability to exercise impartial, unbiased professional care when reviewing case files. - Ability to perform tasks within a fast-paced environment and limited supervision. - Excellent verbal and written communication skills and collaboration with team members. - Understanding the importance and handling of personally identifiable information, particularly health and/or income related information. Requirements - Demonstrated experience with CDBG-DR housing programs and/or experience with housing policy, materials, and processes. - Demonstrated experience with document verification, quality assurance and control, and/or appeals processing will also be considered a preferred qualification. - Experience with MS Office and Adobe Reader. Benefits - Hourly rate based on experience and location: $28.84 - $31.25/hr - 10 paid Holidays - Vacation Pay - Sick Pay - 401 (K) plan with matching - Company paid STD and LTD

Title: Senior Specialist, Regulatory Location: Avon Lake United States Job Description: Avient Corporation seeks Senior Regulatory Specialist at its facility located at 33587 Walker Rd, Avon Lake, OH 44012. JOB DESCRIPTION: Support US and Canada regional customer inquiries related to Avient products meeting various global regulations. Identify and recommend steps to mitigate the impact of impending regulatory changes on Avient’s portfolio. Work with suppliers to maintain all required raw material regulatory information. Assist in the development, implementation, and maintenance of the product regulatory information systems, including SAP EH&S modules on product safety, HazComm, dangerous goods, etc. Hybrid telecommuting permitted: 3 days per week in office required. Responsibilities This position requires a Bachelor’s degree or foreign equivalent in Chemistry, Biology, Environmental Science, or a related field, plus 5 years of experience as a Regulatory Specialist, Data Manager, Product Steward, or related occupation. Additionally, the applicant must have employment experience with: (1) Applying all applicable regulations related to Hazard Communication (North America, Europe, Asia, etc.), such as GHS, EU CLP and other regional regulations; (2) Working with North American regulatory agencies such as EPA, FDA, or FIFRA to assist in product registrations, and submissions; (3) Maintaining all relevant product information within the SAP EH&S Module and other PS systems provide data for various reports; (4) Obtaining and maintaining compliance information on various raw materials to support customer requests related to REACH, RoHS, TSCA, Prop 65; and (5) Working with manufacturing plants to provide guidance on best practices to maintain regulatory compliance and providing training to end-users. #LI-DNI About Us Our purpose at Avient Corporation is to be an innovator of materials solutions that help our customers succeed, while enabling a sustainable world. Innovation goes far beyond materials science; it’s powered by the passion, creativity, and diverse expertise of 9,000 professionals worldwide. Whether you’re a finance wizard, a tech enthusiast, an operational powerhouse, an HR changemaker, or a trailblazer in materials development, you’ll find your place at Avient. Join our global team and help shape the future with sustainable solutions that transform possibilities into realities. Your unique perspective could be the key to our next breakthrough! We believe that all of our global employees are leaders and that the six most important behaviors for driving our strategy and culture are the same no matter if an employee is a leader of self, a leader of others, or a leader of the business. By playing to win, acting customer centric, driving innovation and profitable growth, collaborating seamlessly across Avient, and motivating and inspiring and developing others and yourself you will accelerate your ability to achieve Avient’s strategic goals, to meet our customer needs, and to accomplish your career goals. At Avient, we believe a wide variety of thoughts, ideas and backgrounds gives us the creativity to be successful in a rapidly changing world. In support of this, we stress equality of opportunity for all qualified individuals in accordance with applicable laws. Decisions on hiring, promotion, development, compensation or advancement are based solely on a person’s qualifications, abilities, experience and performance.

Role Description Healthcare delivery is rapidly evolving, and within Optum Whole Health Solutions, the Site Visit Clinician supports provider quality, operational readiness, and consistent performance across the network. The role combines analytics, provider engagement, operational assessment, and quality improvement to strengthen the provider experience and reinforce key standards. Work in this role is generally self-directed and not highly prescribed. The clinician works through less structured and moderately complex issues, assesses provider needs, interprets requirements, and identifies solutions to non-standard situations. The role involves translating developing concepts and quality expectations into practical site review activities and conducting analyses that support clear, actionable findings. The Site Visit Clinician also serves as a resource to others by providing explanations on difficult issues, offering guidance as needed, and supporting colleagues with less experience. The clinician works with minimal guidance and seeks input only on the most complex tasks. As a Site Visit Clinician, you will carry out the full lifecycle of ABA site reviews, including: - Pre-visit planning - Data integration - Onsite assessment - Post-visit reporting - Follow-up on quality action plans Since this work is early in its development and ABA quality standards continue to evolve, success requires comfort with ambiguity, critical thinking, and the ability to apply emerging standards in real provider settings. You’ll enjoy the flexibility to work remotely from anywhere within the U.S. as you take on some tough challenges. Qualifications - Holds active Board Certified Behavior Analyst® (BCBA®) certification in good standing - If required by the state of residence, maintain unrestricted and in good standing licensure and certification - Direct experience delivering applied behavior analysis (ABA) services in clinic, home, or community-based settings - Experience in provider quality oversight, operational review, clinical operations, or similar healthcare support functions - Deep working understanding of Council of Autism Service Providers (CASP) standards of care - Familiar with Autism Commission on Quality (ACQ) accreditation standards - Ability to independently integrate data from multiple sources - Proven ability to communicate clearly in both written and verbal formats - Proven ability to manage multiple workflows with accuracy and attention to detail - Proven capability of interpreting and presenting complex data - Proven solid interpersonal and collaboration skills - Ability to travel up to 40% to conduct onsite provider reviews Requirements - Completes site visits - Performs end-to-end coordination of ABA site reviews - Applies a disciplined, standardized approach to data integration, documentation, and quality verification - Maintains and continuously improves the Integrated Checklist List (ICL) - Coordinates all preparatory activities and confirms documentation completeness - Collects, analyzes, interprets, and synthesizes quantitative and qualitative data - Develops concise pre-visit summaries - Prepares tables, graphs, and interpretive narratives - Participates in pre-visit planning meetings - Serves as an onsite reviewer conducting structured interviews - Documents observations aligned with practice standards - Collaborates with a cross-disciplinary site visit team - Solves moderately complex issues in real-time - Integrates pre-visit data into clear post-visit summaries - Produces actionable written reports - Supports Quality Action Plans - Plans and manages personal workload to align site review assignments - Applies ABA standards of care during site reviews Benefits - Comprehensive benefits package - Incentive and recognition programs - Equity stock purchase - 401k contribution Company Description At UnitedHealth Group, our mission is to help people live healthier lives and make the health system work better for everyone. We believe everyone–of every race, gender, sexuality, age, location, and income–deserves the opportunity to live their healthiest life. We are committed to mitigating our impact on the environment and enabling and delivering equitable care that addresses health disparities and improves health outcomes.

• Review requests and contracts; prepares applications for potential wholesale investors and makes recommendations to appropriate senior management • Responsible for communicating and training branch personnel regarding appropriate company product related programs • Remain current on all product programs and provide updates to branch personnel as applicable • Maintain and update information on company portal with regard to programs • Partner directly with MI companies to resolve any underwriting issues or concerns • Maintain a professional image and adhere to standards consistent with company policies and procedures • Other duties as assigned or required