Sterilization Specialist Jobs Near Me

Why We're Here: At Brave Health, we are driven by a deep commitment to transform lives by expanding access to compassionate, high-quality mental health care. By harnessing the power of technology, we break down barriers and bring mental health treatment directly to those who need it most-wherever they are. As a community health-centered organization, we are dedicated to ensuring that no one is left behind. Nearly 1 in 4 people in the U.S. receive healthcare through Medicaid, yet two-thirds of providers don't accept it. Brave Health is stepping up to close this gap by making mental health care accessible, affordable, and life-changing for all. Requirements: Brave's Quality Assurance Specialists must reside in Florida and have an active LMHC, LCSW, or LMFT to get started. Master's degree in a relevant field (e.g., Social Work, Counseling, Psychology). Licensed in a clinical discipline (e.g., LCSW, LMHC, LMFT). Ability to work independently and collaboratively in a team-oriented environment. Licensed, or willing to become licensed, in additional states that Brave Health serves. Enjoys technology and adopts learning new systems well. Experience with electronic health record (EHR) systems. Previous experience in behavioral health or therapy documentation. Documentation Review: Thoroughly review treatment plans, progress notes, and other documentation submitted by associate therapists (licensed interns). Verify that documentation is accurate, complete, and complies with relevant regulatory standards and organizational guidelines. Compliance Assurance: Monitor and ensure compliance with all applicable laws, regulations, and accreditation standards in the healthcare industry. Stay up-to-date with industry changes and inform the team in the most effective ways about any updates affecting documentation requirements. Quality Control: Conduct regular audits to assess the quality of documentation and identify areas for improvement. Provide constructive feedback to associate therapists and collaborate with them to enhance the quality of their documentation. Collaboration: Work closely with the leadership team, including clinical supervisors and management, to address any issues related to documentation quality and compliance. Communicating effectively with providers for documentation coaching and revision purposes prior to co-signature. Relaying ongoing and urgent matters to CCQAM and other appropriate parties. Foster a collaborative environment that encourages open communication and continuous improvement. Record Keeping: Maintain accurate records of all documentation reviews, feedback provided, and corrective actions taken. Generate reports on the overall quality of documentation and compliance levels. Benefits: Our team works 100% remotely from their own homes! Part-time W2 hourly position Monday - Friday schedule; No on-call or weekends! All equipment provided Brave Health is very proud of our diverse team who cares for a diverse population of patients. We are an equal opportunity employer and encourage all applicants from every background and life experience to apply.

M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed research sites across the country, M3 Wake Research is one of the largest independent, multi-site clinical research companies in the US. M3 Wake Research continues to grow through acquisitions and uncompromising commitment to careful planning and execution in accordance with regulatory compliance. Conducting studies since 1984, M3 Wake Research owns a proprietary patient database of potential clinical trial participants across the US. As of today, our board-certified physicians have completed more than 7,000+ successful clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness, subject enrollment, human protection, and expeditious delivery of accurate evaluable data. Due to our continued growth, we are hiring a Quality Assurance Specialist at Wake Research, an M3 company. This is a remote position with up to 40% travel. The Quality Assurance Specialist will conduct comprehensive quality assurance reviews in support of M3 Wake Research's clinical teams. This role involves collaborating with clinical research staff to address findings, provide recommendations for improvement, and ensure compliance within their area of expertise. The Quality Assurance Specialist will oversee audits and inspections, and work cross-functionally to support continuous quality enhancement across the organization. Essential Duties and Responsibilities: Including, but not limited to the following: * Travel to M3 Wake Research sites to conduct internal quality assurance reviews of clinical trials and processes for adherence to SOPs, company policy, and regulations/standards. * Prepare reports and discuss non-compliance and/or quality findings with internal customers as well as with Quality management. Track and follow up on the resolution of review findings. * Provide guidance to clinical staff in resolving findings, implementing processes, and CAPA plans to include development, root case analysis, implementation, and evaluation of CAPA plans. * Work closely with assigned clinical teams and site directors to identify gaps and ensure continuous process improvement in conjunction with Quality management. * Assist in preparing for inspections by sponsors and regulatory agencies and participate in on site regulatory inspections as appropriate. * Assist in implementing quality management plans including risk identification and assessment through data review and quality control processes. * Provides consultation on corrective and preventive actions performed as a result of observations; follows-up and provides data required to determine the timeliness and effectiveness of corrective and preventive actions performed by the site staff and operational team. Assist with the development or enhancement of training materials. * Conducts on-the-job training (OJT) and instructor-led training (ILT) for employees and new hires. * Conduct review of training records to ensure assigned sites are maintaining compliance with training curriculum. * Remain informed about developments in relevant clinical trial requirements, FDA, ICH, GCP, and guidelines within the US and other regions, as appropriate for M3 Wake Research. * Identify and escalate significant compliance issues. * Share quality topics and lessons learned to the organization. * Assist individual sites in development of internal guidance documents to supplement corporate SOPs. * Assist with quality incident and compliance investigations. Qualifications * Bachelor's degree or equivalent experience * Sound working knowledge of medical terminology, Standard Operating Procedures (SOPs), International Conference on Harmonization (ICH), Good Clinical Practice (GCP), Food and Drug Administration (FDA), applicable regulatory requirements, and quality management processes. * 3-5 years prior work experience in a clinical quality, clinical compliance, or clinical auditing role. * Direct experience in the conduct and reporting of internal and external audits preferred. * Experience preparing for, participating in, and subsequent response to health authority GCP inspections/partner audits also preferred. * Clinical Research or Quality Certification preferred. * Excellent interpersonal, verbal, and written communication skills. * Client focused approach. * Ability to work independently, take initiative, and have a flexible approach with respect to work assignments and new learning. * Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail and strong organizational skills. * Ability to work effectively in a matrix environment and to demonstrate and foster teamwork within the group as well as across the organization. * Proficient in Microsoft Office programs such as MS Word, Outlook, Excel, PowerPoint, SharePoint, and Teams. * Fully and consistently able to demonstrate tact, diplomacy, discretion, and good judgment. Additional Information About M3USA M3 USA is at the forefront of healthcare innovation, offering digital solutions across healthcare, life sciences, pharmaceuticals, and more. Since our inception in 2000, we've seen remarkable growth, fueled by our mission to utilize the internet for a healthier world and more efficient healthcare systems. Our success is anchored in our trusted digital platforms that engage physician communities globally, facilitating impactful medical education, precise job placement, and insightful market research. M3 USA prides itself on a dynamic and innovative work environment where every team member contributes to global health advancements. Joining M3 USA means being part of a dedicated team striving to make a significant difference in healthcare. We provide a unique opportunity for you to be at the cutting edge of healthcare innovation, shaping the future in a meaningful career. Embrace the chance to drive change with M3 USA. Benefits: A career opportunity with M3 Wake Research offers competitive wages, and benefits such as: * 401(k), 401(k) matching * Dental insurance * Disability insurance * Employee assistance program * Flexible spending account * Health insurance * Life insurance * Paid time off * Vision insurance * M3 reserves the right to change this job description to meet the business needs of the organization #LI-Remote #LI-LB1

M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed research sites across the country, M3 Wake Research is one of the largest independent, multi-site clinical research companies in the US. M3 Wake Research continues to grow through acquisitions and uncompromising commitment to careful planning and execution in accordance with regulatory compliance. Conducting studies since 1984, M3 Wake Research owns a proprietary patient database of potential clinical trial participants across the US. As of today, our board-certified physicians have completed more than 7,000+ successful clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness, subject enrollment, human protection, and expeditious delivery of accurate evaluable data. Due to our continued growth, we are hiring a Quality Assurance Specialist at Wake Research, an M3 company. This is a remote position with up to 40% travel. The Quality Assurance Specialist will conduct comprehensive quality assurance reviews in support of M3 Wake Research's clinical teams. This role involves collaborating with clinical research staff to address findings, provide recommendations for improvement, and ensure compliance within their area of expertise. The Quality Assurance Specialist will oversee audits and inspections, and work cross-functionally to support continuous quality enhancement across the organization. Essential Duties and Responsibilities: Including, but not limited to the following: Travel to M3 Wake Research sites to conduct internal quality assurance reviews of clinical trials and processes for adherence to SOPs, company policy, and regulations/standards. Prepare reports and discuss non-compliance and/or quality findings with internal customers as well as with Quality management. Track and follow up on the resolution of review findings. Provide guidance to clinical staff in resolving findings, implementing processes, and CAPA plans to include development, root case analysis, implementation, and evaluation of CAPA plans. Work closely with assigned clinical teams and site directors to identify gaps and ensure continuous process improvement in conjunction with Quality management. Assist in preparing for inspections by sponsors and regulatory agencies and participate in on site regulatory inspections as appropriate. Assist in implementing quality management plans including risk identification and assessment through data review and quality control processes. Provides consultation on corrective and preventive actions performed as a result of observations; follows-up and provides data required to determine the timeliness and effectiveness of corrective and preventive actions performed by the site staff and operational team. Assist with the development or enhancement of training materials. Conducts on-the-job training (OJT) and instructor-led training (ILT) for employees and new hires. Conduct review of training records to ensure assigned sites are maintaining compliance with training curriculum. Remain informed about developments in relevant clinical trial requirements, FDA, ICH, GCP, and guidelines within the US and other regions, as appropriate for M3 Wake Research. Identify and escalate significant compliance issues. Share quality topics and lessons learned to the organization. Assist individual sites in development of internal guidance documents to supplement corporate SOPs. Assist with quality incident and compliance investigations. Qualifications Bachelor's degree or equivalent experience Sound working knowledge of medical terminology, Standard Operating Procedures (SOPs), International Conference on Harmonization (ICH), Good Clinical Practice (GCP), Food and Drug Administration (FDA), applicable regulatory requirements, and quality management processes. 3-5 years prior work experience in a clinical quality, clinical compliance, or clinical auditing role. Direct experience in the conduct and reporting of internal and external audits preferred. Experience preparing for, participating in, and subsequent response to health authority GCP inspections/partner audits also preferred. Clinical Research or Quality Certification preferred. Excellent interpersonal, verbal, and written communication skills. Client focused approach. Ability to work independently, take initiative, and have a flexible approach with respect to work assignments and new learning. Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail and strong organizational skills. Ability to work effectively in a matrix environment and to demonstrate and foster teamwork within the group as well as across the organization. Proficient in Microsoft Office programs such as MS Word, Outlook, Excel, PowerPoint, SharePoint, and Teams. Fully and consistently able to demonstrate tact, diplomacy, discretion, and good judgment. Additional Information About M3USA M3 USA is at the forefront of healthcare innovation, offering digital solutions across healthcare, life sciences, pharmaceuticals, and more. Since our inception in 2000, we've seen remarkable growth, fueled by our mission to utilize the internet for a healthier world and more efficient healthcare systems. Our success is anchored in our trusted digital platforms that engage physician communities globally, facilitating impactful medical education, precise job placement, and insightful market research. M3 USA prides itself on a dynamic and innovative work environment where every team member contributes to global health advancements. Joining M3 USA means being part of a dedicated team striving to make a significant difference in healthcare. We provide a unique opportunity for you to be at the cutting edge of healthcare innovation, shaping the future in a meaningful career. Embrace the chance to drive change with M3 USA. Benefits: A career opportunity with M3 Wake Research offers competitive wages, and benefits such as: 401(k), 401(k) matching Dental insurance Disability insurance Employee assistance program Flexible spending account Health insurance Life insurance Paid time off Vision insurance *M3 reserves the right to change this job description to meet the business needs of the organization #LI-Remote #LI-LB1

Arcadis is the world's leading company delivering sustainable design, engineering, and consultancy solutions for natural and built assets. We are more than 36,000 people, in over 70 countries, dedicated to improving quality of life. Everyone has an important role to play. With the power of many curious minds, together we can solve the world's most complex challenges and deliver more impact together. Role description: Arcadis is seeking an experienced Environmental Regulatory Compliance Specialist to join our Sustainable Operations team in the Northeast (Columbus Ohio area). This position will support national and regional Environmental and/or Health & Safety regulatory compliance, auditing, and permitting projects. This will be a hybrid/remote role with approximately 25% travel and 75% office work (hybrid or remote). Candidates will have a minimum of 3 years of experience and a bachelor's degree in environmental engineering, environmental science, or other directly relevant EHS compliance disciplines. As a Consultant with Arcadis, you'll soon discover you can make a difference in our company by collaborating with staff and contributing to an interesting array of projects. You will be a key member to drive innovation and build strong technical communities within the EHS Space. This is a great opportunity to work with a dynamic team and gain experience in a wide variety of environmental projects for diverse market sectors. Your career growth will only be limited by your skills and your passion for success! Role accountabilities: As an Environmental Scientist or Engineer, you will work directly with senior engineers and scientists on compliance, permitting, and reporting projects. You will provide support to our key clients with focus on clients in the Ohio, Indiana, and Pennsylvania area. You will assist clients with permitting and compliance strategies, preparation of regulatory permit applications, and develop environmental or health & safety compliance policies, programs, procedures, and management systems. You may perform or assist with site visits, compliance audits, trainings, and meetings. You may prepare emissions or process inventories and other annual reporting, such as Toxics Release Inventory Reporting and Tier II. You will have the opportunity to participate in all areas of environmental compliance such as air, water, waste management, stormwater permitting and SPCC plans. Primary responsibilities will require environmental compliance experience; however, knowledge/background of health & safety is also preferred. Collaborate with Arcadis' compliance team to ensure application of regulatory knowledge, analytical techniques, and excellent project delivery. Be mentored by senior members of the EHS team from a technical and business prospective and to ensure all work products meet Arcadis quality standards. Interact with clients, understanding their needs, and conversing with regulators on their behalf Proficiency in Microsoft Word, Excel and PowerPoint to edit and develop professional technical documents and perform data analysis. Ability to travel (up to 25%) for project and client needs; however, most work will be performed from an Arcadis office location or remotely. Qualifications & Experience: Required Qualifications Minimum of 3 years of relevant experience. BS in Environmental Engineering, Environmental Science, EHS Management, or other directly relevant EHS compliance disciplines. Knowledge of federal, state and local environmental compliance regulations including air quality, stormwater, wastewater, hazardous, universal and solid waste, chemical and oil management Preferred Qualifications Knowledge of federal, state and local health & safety compliance regulations Registrations/Certifications: BEAC, CHMM, PE, ISO Lead Auditor Knowledge of Management Systems (ISO 14001, 50001, 45001) Why Arcadis? We can only achieve our goals when everyone is empowered to be their best. We believe everyone's contribution matters. It's why we are pioneering a skills-based approach, where you can harness your unique experience and expertise to carve your career path and maximize the impact we can make together. You'll do meaningful work, and no matter what role, you'll be helping to deliver sustainable solutions for a more prosperous planet. Make your mark, on your career, your colleagues, your clients, your life and the world around you. Together, we can create a lasting legacy. Join Arcadis. Create a Legacy. Our Commitment to Equality, Diversity, Inclusion & Belonging We want you to be able to bring your best self to work every day which is why we take equality and inclusion seriously and hold ourselves to account for our actions. Our ambition is to be an employer of choice and provide a great place to work for all our people. We are an equal opportunity and affirmative action employer. Women, minorities, people with disabilities and veterans are strongly encouraged to apply. We are dedicated to a policy of non-discrimination in employment on any basis including race, creed, color, religion, national origin, sex, age, disability, marital status, sexual orientation, gender identity, citizenship status, disability, veteran status, or any other basis prohibited by law. Arcadis offers benefits for full time and part time positions. These benefits include medical, dental, and vision, EAP, 401K, STD, LTD, AD&D, life insurance, paid parental leave, reward & recognition program and optional benefits including wellbeing benefits, adoption assistance and tuition reimbursement. We offer nine paid holidays and 15 days PTO that accrue per year. The salary range for this position is $70800 - $106200. Actual salaries will vary and are based on several factors, such as experience, education, budget, internal equity, project and location. #LI-SC1 #Resilience-NA #Environment-NA

***Please note this is a full-time, fully remote or hybrid opportunity in Ventura, CA. or Chesapeake, VA., depending on your preference***Job Summary: VSolvit is seeking a skilled Quality Assurance Specialist to join our dynamic team supporting our U.S. Navy customer. In this role, you will be assisting our government software development projects in achieving and maintaining compliance with our corporate CMMI, ISO and CMMC initiatives. As with any position, additional expectations exist. Some of these include, but are not limited to, adhering to normal working hours, meeting deadlines, following company policies as outlined by the Employee Handbook, communicating regularly with assigned supervisor(s), staying focused on the assigned tasks, and completing other tasks as assigned. Responsibilities: Maintain and/or create the company's version-controlled documents in accordance with defined policies and procedures Perform audits on the development team(s) and their projects to ensure compliance with CMMI-Dev/Services Level III requirements Perform gap analysis between software team processes and CMMI-Dev/Services Level III requirements Establish and maintain procedures necessary to assist the projects in creating and maintaining audit ready documentation Work cooperatively with our Quality Management group to sustain the companies CMMI and ISO registrations Assist and/or perform internal process audits to ensure the CMMI and ISO audit readiness of the internal project team Develop audit plan, document non-conformances(s) and report non-conformance(s) to management Addressing nonconformities from previous internal and external audits Basic Qualifications: Must be a U.S. Citizen Bachelor's degree in Business or Technology (or related area). 4+ years of experience may substitute for degree 3+ years Quality Systems Document Control or other Quality Assurance related experience Excellent communication and analytical skills, written and oral Working knowledge of word-processing and integrated software applications Organizational skills and ability to perform detail-oriented work are required Must be able to resolve problems independently or work with team members to drive solutions Hold an Active DoD Secret Clearance Preferred Qualifications: 3+ years Document Control or other Quality Assurance related experience Experience with Quality Systems Documentation and excellent documentation practices Knowledge of CMMI-Dev/Services/Data Maturity Level III requirements (v. 2.0 or 3.0) and ISO27K/20K control standards Demonstrated ability in identifying, evaluating and/or defining compliance requirements in a technical environment Possess strong negotiation skills with a “can-do” attitude and be able to motivate stakeholders Meticulous in detail and a track record of delivering regulatory documentation Must be able to meet deadlines and changing priorities Strong communication and verbal skills Familiarity with software development environments including Agile/Scrum SDLC Company Summary:Join the VSolvit Team! Founded in 2006, VSolvit (pronounced 'We Solve It') is a technology services provider that specializes in cybersecurity, cloud computing, geographic information systems (GIS), business intelligence (BI) systems, data warehousing, engineering services, and custom database and application development. VSolvit is an award winning WOSB, CA CDB, MBE, WBE, and CMMI Level 3 certified company. We offer a customizable health benefits program that best meets the needs of its employees. Offering may include: medical, dental, and vision insurance, life insurance, long and short-term disability and other insurance products, Health Savings Account, Flexible Spending Account, 401K Retirement Plan options, Tuition Reimbursement, and assorted voluntary benefits. Our goal is to grow together and enjoy the work that we do as a team. VSolvit LLC is an Equal Opportunity/Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status.

The Company Serving the People Who Serve the People Granicus is driven by the excitement of building, implementing, and maintaining technology that is transforming the Govtech industry by bringing governments and their constituents together. We are on a mission to support our customers by meeting the needs of their communities and implementing our technology in ways that are equitable and inclusive. Granicus has consistently appeared on the GovTech 100 list over the past 5 years and has been recognized as the best companies to work on BuiltIn. Over the last 25 years, we have served 5,500 federal, state, and local government agencies and more than 300 million citizen subscribers powering an unmatched Subscriber Network that uses our digital solutions to make the world a better place. With comprehensive cloud-based solutions for communications, government website design, meeting and agenda management software, records management, and digital services, Granicus empowers stronger relationships between government and residents across the U.S., U.K., Australia, New Zealand, and Canada. By simplifying interactions with residents, while disseminating critical information, Granicus brings governments closer to the people they serve-driving meaningful change for communities around the globe. Want to know more? See more of what we do here. The QA Specialist is responsible for quality assurance audits and ensures that the website implementation standards are met. Keen attention to detail, master prioritization skills, versatility, and passion for delivering world-class solutions are cornerstones for this role. Candidates should bring a consultative approach and a "whatever it takes" attitude. In this role, you will document functional tests, perform testing assignments, investigate operational and accessibility problems, and perform the QA process. #PuertoRicoCostaRica What your impact will look like here Ensure consistency between the base wireframe, design, technical specifications, and website Note and track any issues discovered during this process, and ensure a timely resolution Document the process and testing scenarios Identify consistent trends that decrease quality, find an appropriate resolution, and develop the strategy to mitigate future instances Manage a backlog of QA tasks assigned to you with a focus on project priority Ensure up-to-date communication with the Project Management and Development teams Research current advancements in QA processes, and adapt our internal QA process Build and analyze reporting on the QA phase (and other phases in development) to aid with consistent delivery timelines Perform periodic checks on the projects' base code to minimize issues upon commencement of the development cycle Assist the development team in resolving tickets in the development task queue by performing basic code edits in HTML or razor code You will love this job if you have Knowledge of WCAG, HTML 5, CSS 3, Mobile-First Responsive Design, and other HTML/CSS standards or techniques Deadline and detail-oriented Experience writing clear, concise, and comprehensive test plans and cases Experience working with relational databases, especially creating test data Experience with automated testing platforms Deep understanding and experience in QA methodologies, tools, and practices Working knowledge of one or more programming/scripting languages Ability to understand complex systems and triage issues based on that knowledge Must have client-facing experience Excellent communication skills Experience working with or for local government or govtech a plus Responsible for "Company" information security by appropriately preserving the Confidentiality, Integrity, and Availability (CIA) of "Company" information assets in accordance with the company's information security program. Don't have all the skills/experience mentioned above? At Granicus, we are trying to build diverse, inclusive teams. We do not have degree requirements for most of our roles. If you don't meet every requirement above but are excited to learn more, we encourage you to apply. We might just be able to find another role that could be a perfect fit! Security and Privacy Requirements - Responsible for Granicus information security by appropriately preserving the Confidentiality, Integrity, and Availability (CIA) of Granicus information assets in accordance with the company's information security program. - Responsible for ensuring the data privacy of our employees and customers, their data, as well as taking all required privacy training in a timely manner, in accordance with company policies. The Team - We are a remote-first company with a globally distributed workforce across the United States, Canada, United Kingdom, India, Armenia, Australia, and New Zealand. The Culture - At Granicus, we are building a transparent, inclusive, and safe space for everyone who wants to be a part of our journey. - A few culture highlights include - Employee Resource Groups to encourage diverse voices - Coffee with Mark sessions - Our employees get to interact with our CEO on very important and sometimes difficult issues ranging from mental health to work-life balance and current affairs. - Microsoft Teams communities focused on wellness, art, furbabies, family, parenting, and more.-=- - We bring in special guests from time to time to discuss issues that impact our employee population The Impact - We are proud to serve dynamic organizations around the globe that use our digital solutions to make the world a better place - quite literally. We have so many powerful success stories that illustrate how our solutions are impacting the world. See more of our impact here. Granicus is committed to providing equal employment opportunities. All qualified applicants and employees will be considered for employment and advancement without regard to race, color, religion, creed, national origin, ancestry, sex, gender, gender identity, gender expression, physical or mental disability, age, genetic information, sexual or affectional orientation, marital status, status regarding public assistance, familial status, military or veteran status or any other status protected by applicable law.

MiCo2 Group, LLC is currently seeking agents for Quality Assurance Specialists. Provide feedback on the level of customer service and processes for various companies! We are recruiting exceptional independent contractors to provide their insight while working from home. This is a part-time opportunity! You will be contacting companies based on general assignments. You WILL NOT be required to make any purchases, commitments or provide personal information. You will set your own schedule, so you can work anytime that fits YOUR schedule to meet the deadline. RequirementsResponsibilities: * Complete a test call successfully * Call all companies provided via assigned lists * Evaluate the level of customer service provided by answering representative * Document detailed information of overall experience * Complete review submission form before the required deadline * Ensure that form is free of errors and misinformation Requirements: * Must have valid United States Identification * Minimum 6 months customer service experience, preferably call center related * Moderate level of computer knowledge * Ability to work with minimal supervision * Must be self-directed and self-motivated * Strong listening skills * Accuracy * Efficiency * Excellent written and verbal communication skills Technical Requirements • Active Phone line (mobile or landline) • Mobile Device capable of downloading applications • CPU (Intel or AMD) 2GHz processor (or equivalent) • Resolution of 1,280 x 720 (720p) or greater • Internet Explorer 9.0 or higher BenefitsSave on gas Save on time

Job Brief: We are looking for a Quality Assurance Specialist to join our team and oversee the quality of all products and services that our organization produces. Quality Assurance Specialist responsibilities include developing quality standards, conducting tests and identifying issues in the production of our products or services. Ultimately, you will work with a team to ensure our final products meet our organization's standards across the board. Responsibilities: Ensure that standards and safety regulations are observed Address and discuss issues and proposed solutions with superiors Document quality assurance activities and create audit reports Make recommendations for improvement Create training materials and operating manuals Requirements and skills: Proven work experience as a Quality Assurance Specialist or similar role Working knowledge of tools, methods and concepts of quality assurance Solid knowledge of relevant regulatory standards Good communication skills, both verbal and written Excellent data collection and analysis skills Strong attention to detail Relevant training and/or certifications as a Quality Assurance Specialist Tools Provided for remote work: Internet access Phone Computer 2TB hard drive Printer Benefits: Health Care Plan (Medical, Dental & Vision) Life Insurance (Basic, Voluntary & AD&D) Paid Time Off (Vacation, Sick & Public Holidays) Short Term & Long Term Disability Training & Development Work From Home Stock Option Plan Salary: $67,000 - $72,0000

As a QA Generalist, you will be an integral part of the Quality & Compliance team, ensuring high-quality standards in accordance with applicable laws, regulations, and internal policies. This role involves supporting quality assurance processes, ensuring regulatory compliance, and collaborating with cross-functional teams to maintain product integrity and safety. A solid understanding of both laboratory and manufacturing environments within the biotechnology industry is essential. Responsibilities * Perform batch record review and release in support of US and ex-US clinical trials. * Investigate and address product quality issues, including deviations, OOS results, and non-conformances. * Collaborate with CDMOs and internal CMC teams to ensure quality standards are met from development through commercialization. * Provide quality support to CMC throughout the product lifecycle. * Implement, maintain, and improve the Quality Management System (QMS) in accordance with internal policies, regulatory requirements, and industry standards. * Assist in the creation and maintenance of SOPs, policies, and associated documents. * Compile metrics for internal and external operations. * Support the management of document control processes, including reviewing and approving batch records, deviation reports, and change controls. * Ensure that all documentation is accurate, complete, and compliant with internal policies, procedures, and regulatory standards. * Assist in preparing for internal and external audits. * Support the execution of internal audits to ensure compliance with regulatory standards. * Address and resolve audit findings, ensuring corrective actions are implemented. * Assist in the preparation of regulatory filings and submissions. * Perform other related duties as assigned. Essential Skills * Extensive knowledge of GMP, GCP ICH, and US/EU/UK regulations. * Experience in drug manufacturing or biologics industry in Quality Assurance, Quality Control, or Quality Engineering positions. * Demonstrated knowledge of Quality Management Systems, preferably electronic systems. * Bachelor's Degree in Life Sciences (Biology, Biochemistry, Biotechnology, etc.) or a related field. * Minimum of 4 years' experience in biopharmaceutical operations, technical operations, and/or quality operations, with 2+ years of hands-on experience in Quality function supporting clinical or commercial batch release. * Experience supporting product technical transfer activities and comparability studies. * Experience with audit processes, document control, and Quality Management Systems: deviations, change control management, and CAPAs. * Strong interpersonal and leadership skills with the ability to build and maintain effective professional relationships. * Effective presentation and writing skills. * Ability to provide clear, pragmatic direction and advice regarding compliance issues. * Highly organized and able to work independently. * Strong team orientation and passion for continuous self-development. Additional Skills & Qualifications * Cell and gene therapy experience preferred. * Experience in a startup environment preferred. Work Environment This position offers flexibility with hours and the opportunity to work remotely. You will be part of a small team within the Quality Management System, working alongside a manager and director. The biotech company is working towards pivotal trials, and the leadership team has remained consistent over the past 8 years. Our benefits include accrued PTO, holiday pay, and accrued sick pay. Pay and Benefits The pay range for this position is $32.00 - $40.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a hybrid position in Philadelphia,PA. Application Deadline This position is anticipated to close on Feb 7, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

OneSource Virtual (OSV) has helped more than 1,000 Workday customers take their teams from transactional to transformational with innovative technology and services for HR, payroll, and finance. Founded in 2008, OSV is the leading exclusive provider of Business-Process-as-a-Service (BPaaS) solutions for Workday, delivering services with unparalleled choice, unwavering commitment, and uncompromising support. OneSource Virtual's global headquarters is located in Dallas, Texas, with additional locations across North America and Europe. Find your company's solution at ************************* *** This is not a Tech or IT role. This is a Leave of Absence in employee benefits position. *** Must have hands on experience working in Leave of Absence. Position Summary/Objective The Quality Assurance Specialist is responsible for ensuring quality across the employee services department for both internal and external customers. Essential Functions/Duties/Responsibilities · Provides professional and timely service to internal and external customers in a call center environment · Effective communication skills via telephone, email and in-person · Ability to perform quality reviews of team tickets and call recordings and provide objective, consistent and documented feedback · Prepare and participate in ongoing calibration sessions with customers · Resolve Quality issues and escalations from internal and external customers · Support all organization and departmental initiatives around quality and improving the customer experience · Participate in ongoing training relative to the functional area and tools · Form strong partnerships within the department and organization · Meets or exceeds all performance standards · Assumes other duties as assigned by Manager Competencies · Analytical skills; strong research and follow up skills · Attention to detail · Customer service experience · Ability to multi-task · Professional communication skills · Ability to work independently · Flexible · Ability to make decisions utilizing sound judgment · Must value and promote team spirit, have outstanding interpersonal skill set; exhibit professionalism within the workplace; maintain punctuality and adherence to set schedule; have solid research and follow-up skills. · Must be able to cope in fast-paced, demanding environment and manage sensitive, confidential issues · Maintain punctuality and adherence to set schedule with extra hours as needed Supervisory Responsibility This position has no supervisory responsibilities Qualifications and Experience · High School degree required · 3+ years of related experience and/or training · Customer Service experience preferred · Must have knowledge of LOA; knowledge of federal regulations · Proficient PC Skills (Microsoft Office, Outlook, HRIS, etc…) Preferred Skills · Prior Service Center QA Experience · Bachelor's degree #LI-REMOTE You are encouraged to learn and share ideas when you join the OneSource Virtual team. We reward innovative thinking, fresh perspectives, creative collaboration, and hard work. As an organization experiencing routine strategic growth, we are always on the lookout for intelligent, talented, and forward-thinking professionals to join our team. OSV employees enjoy a values-based culture, upward mobility, and professional development with opportunities of all kinds.

At Totara, our strength is the efficiency with which we deliver innovative products and support to our customers. We are setting the standard for success in our industry. To help us continue our growth, we are seeking a detail-oriented and highly skilled Business Analyst with QA Testing Responsibilities to join our team. This hybrid role involves analyzing business requirements, identifying solutions, and ensuring the quality and functionality of software applications. You will work closely with stakeholders to understand business needs and translate them into clear, actionable requirements, while also leading testing efforts to ensure the delivery of high-quality products. The ideal candidate will possess both strong analytical skills and a solid understanding of quality assurance methodologies. Responsibilities - Business Analysis: Collaborate with stakeholders to gather, analyze, and document business requirements, functional specifications, and user stories. Work with project managers, developers, and customer teams to define project scope, objectives, and timelines. Translate business needs into technical requirements and ensure alignment with system capabilities. Create process models, use cases, and workflows to clearly communicate requirements. Analyze and document existing processes and systems to identify areas for improvement or optimization. Support the development of project plans, timelines, and deliverables. Act as a liaison between business teams and technical teams to ensure objectives are met. Responsibilities - Quality Assurance Testing: Develop and execute comprehensive test plans and test cases based on technical requirements and functional specifications. Perform functional, regression, integration, and user acceptance testing (UAT) to ensure the quality of software releases. Identify, document, and track defects, ensuring they are communicated to the development team and resolved promptly. Work closely with developers to understand application functionality and to identify testing needs. Coordinate UAT efforts with end users, ensuring that the system meets business expectations. Develop automated test scripts, where applicable, to improve efficiency and effectiveness of testing efforts. Review test results, document issues, and collaborate with stakeholders to drive resolution. Collaboration & Communication: Work closely with cross-functional teams (development, QA, operations, business users) to ensure project success. Maintain clear and consistent communication with project stakeholders to provide regular status updates and report on project progress. Participate in project meetings, reviews, and stand-ups to ensure alignment between business needs and technical solutions. Provide recommendations for process improvements based on testing outcomes and business feedback. Documentation & Reporting: Maintain comprehensive documentation of requirements, test plans, test cases, and defect reports. Generate test reports, including defect summaries, test coverage, and test results for stakeholders. Assist in the creation and maintenance of knowledge bases and user manuals, where applicable. Required Skills Bachelor's degree in Business Administration, Computer Science, Information Technology, or related field or or equivalent work experience 2+ years of experience in a Business Analyst role, with a strong understanding of business processes and requirements gathering. 2+ years of experience in Quality Assurance testing (manual and automated), with a focus on web and/or mobile applications. Skills and Competencies: Strong analytical, problem-solving, and critical-thinking skills. Excellent written and verbal communication skills, with the ability to communicate complex technical concepts to non-technical stakeholders. Proficiency in creating and maintaining detailed documentation (requirements, test cases, test results, etc.). Familiarity with Agile and Waterfall methodologies. Knowledge of SQL and ability to query databases for testing purposes is a plus but not required. Experience in automated testing tools and scripts is a plus but not required. Detail-oriented with strong organizational skills and the ability to prioritize tasks in a fast-paced environment. Ability to work independently and as part of a team to drive project success. Qualities of Success Love of problem solving Collaborative, team-based mindset No excuse demeanor Manages work efficiently (Preparedness, self-directed) Benefits and Perks Unlimited PTO Enhanced Parental Leave Professional Development Opportunities Annual Wellbeing Allowance New Joiner home working set-up allowance Additional Paid Leave: Birthday off, Working days between Christmas and New Years Eve This is a full time, fully remote career opportunity that requires applicants to be in the United States, a U.S. citizen and pass a background check. Some travel may be required.

Responsible for monitoring, reviewing, and proposing measures to correct or improve staff capability and quality Responsibilities Accountable for internal competency of Inpatient/Outpatient Coding staff Develop content for and deliver orientation and training for new associates and ongoing skill-based training for all reviewers Complete quality assurance processes; document and report findings Lead client and reviewer quality communication and resolution Test McBee Clinical Review functionality Act as an expert resource for highly complex or first-of-a-kind reviewer questions; ensure knowledge management resources are available, updated and leveraged. Accountable to communicate quality concerns to all stakeholders Qualifications Required At least 4 years of experience in Inpatient/Outpatient Coding review Expert in ICD-10 coding and guidelines Proficient in Inpatient/Outpatient industry regulations and guidelines Excellent communication and presentation skills Working knowledge of Microsoft Office Preferred Advanced clinical degree Active clinical license (e.g. RN, PT, OT, SP) Netsmart is proud to be an equal opportunity workplace and is an affirmative action employer, providing equal employment and advancement opportunities to all individuals. We celebrate diversity and are committed to creating an inclusive environment for all associates. All employment decisions at Netsmart, including but not limited to recruiting, hiring, promotion and transfer, are based on performance, qualifications, abilities, education and experience. Netsmart does not discriminate in employment opportunities or practices based on race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, age, physical or mental disability, past or present military service, or any other status protected by the laws or regulations in the locations where we operate. Netsmart desires to provide a healthy and safe workplace and, as a government contractor, Netsmart is committed to maintaining a drug-free workplace in accordance with applicable federal law. Pursuant to Netsmart policy, all post-offer candidates are required to successfully complete a pre-employment background check, including a drug screen, which is provided at Netsmart's sole expense. In the event a candidate tests positive for a controlled substance, Netsmart will rescind the offer of employment unless the individual can provide proof of valid prescription to Netsmart's third party screening provider. If you are located in a state which grants you the right to receive information on salary range, pay scale, description of benefits or other compensation for this position, please use this form to request details which you may be legally entitled. All applicants for employment must be legally authorized to work in the United States. Netsmart does not provide work visa sponsorship for this position. Netsmart's Job Applicant Privacy Notice may be found here.

Collabora Productivity We are looking for a detail-oriented and proactive Quality Assurance Specialist to ensure the quality and reliability of our products/services. The ideal candidate will have a strong understanding of QA methodologies, excellent communication skills, and a passion for delivering top-notch solutions. As a QA Specialist, you will collaborate with cross-functional teams to identify and address issues, conduct thorough testing, and contribute to the continuous improvement of our processes. Responsibilities:Find a cause of the issue and test to check the fix works in a complex environment involving multi-tier web applications Perform functional, regression and performance testing to identify and report defects or inconsistencies in product functionality Collaborate with product development and project management teams to understand project requirements and provide input on testability and quality aspects Document and track test results, issues and resolution efforts to ensure clear communication and visibility of QA activities Conduct root cause analysis for identified defects and work with the development team to facilitate timely resolutions Contribute to the establishment and enhancement of quality assurance standards and best practices within the organization Active participation on regular internal QA calls Hands-on troubleshooting sessions with customers via video conferencing and/or remote desktop tools"Can do” attitude in different situations Primary Qualifications:Proven experience in software quality assurance, with a focus on manual testing Strong understanding of QA methodologies, tools and processes4-5 years Linux experience, including compiling software, command line and debugging tools Knowledge and experience of Docker and KubernetesBasic knowledge of version control systems, specifically GitExcellent analytical and problem-solving skills Strong communication and collaboration skills with the ability to work effectively in a team environment Detail-oriented with a commitment to delivering high-quality results Additional Skills:Bachelor's degree in Computer Science, Engineering, or a related field Experience with test automation tools and frameworks is a plus (e.g., Cypress, Cppunit) Experience working in an open source environment is a plus If you are passionate about ensuring the highest level of quality in products/services and are ready to contribute to a dynamic and innovative team, we encourage you to apply. Join us in our commitment to excellence and be a key player in our continued success. #LI-Remote

Details Dearborn, MI Department: Information Technology Reports To: Sr. Manager, IT Delivery COE FLSA Status: Exempt Classification: Remote Job Band: Professional The Quality Assurance Specialist will be part of the Delivery COE team, responsible for the test case development, test execution, analyze results, knowledge transfer for automated testing team, and test result reporting for each new feature assigned to them. The QA Specialist performs functional, system and integration, release, bug/fix and regression tests across browsers, devices, systems and environments related to Carhartt's eComm and Retail applications. They will be integral to creating and maintaining a cohesive, collaborative, success-oriented culture in which we leverage technology industry best practices to meet the needs of our Carhartt associates. We Are All Leaders at Carhartt In our words and by our actions, we strive to emulate the hardworking example set forth by our founder, Hamilton Carhartt. We Lead Business by creating value, delivering on results, and making changes along the way. We Lead Self by being inclusive, recognizing that our differences make us stronger as we strive to build a better world, together, for all hardworking people. We Lead Others by communicating and clearly defining the path as we walk bravely into the future. Working at Carhartt, we are all given a seat at the table and the honor of continuing the legacy. Representative Responsibilities * Create and execute test plans based on business requirements and technical specifications. * Perform a range of testing methods such as functional, integration, regression, end-to-end, usability, and "smoke testing" * Record and document results and compare to expected results. * Identify, document, and track identified defects * Document anomalies and issues. * Support the research and verification of reported defects by our automated testing tool or those reported by staff * Ensure compliance with general programming best practices, accepted web standards and those standards set forth by upstream sources. * Ensure data integrity standards are met. * Perform review, walkthroughs, or inspections. * Facilitate demos for automation testing script creation. * Actively participate in scrums, grooming sessions and sprint retrospectives. Required Education * Bachelor's Degree in Computer Science, IT, Engineering, or related field, or equivalent work experience in lieu of degree. Required Skills & Experience * 3+ years of professional experience developing and executing system release and regression test plans, inclusive of the following: * 1-2 years of Quality Assurance Testing experience for websites or mobile applications * 1+ years of experience writing integration tests plans * 1 year of experience automating test cases or directing automated testing teams, preferred * Experience with testing for cross browser compatibility and layout issues. * Experience in Test Planning, execution, tracking tool (e.g. Test Rail, ADO, etc) * Experience with eComm, Retail and SAP applications, preferred * Ability to create detailed test plans, test cases, test data, test scripts and test reports based on user stories * Excellent attention to detail with a focus on user experience * Strong analytical and problem-solving skills * Strong written and verbal communication, in order to accurately identify and resolve defects/bugs that arise with end users * Excellent organizational and interpersonal skills, including a strong commitment to follow-up, follow-through, and collaborate with cross-functional teams with a sense of urgency * Understanding of Software Development Life Cycle (SDLC) * Basic exposure to Agile and Scrum development processes, inclusive of projects within Agile environments * Experience with Software Testing methodologies and processes * Ability to meet timelines and, and when needed, work under deadlines while maintaining strong attention to detail and quality of your work * Proficiency in Microsoft Word, Excel, PowerPoint * Ability to work in a team environment with coworkers and internal customers Physical Requirements and Working Conditions * Normal office environment. Extended periods of time sitting, standing, typing on a computer is required. * This position has a Remote location: Associate will have no regular requirement to be on-site. Travel on-site is limited to special events. * Carhartt is a tobacco free workplace. #LI-Remote Nearest Major Market: Dearborn Nearest Secondary Market: Detroit

Job Title: Entry-Level Quality Assurance Specialist Part-Time or Full-Time, Remote Pay: $35 per hour Hours: 15-25 hours per week, with potential for up to 35 hours on occasion. Hours are semi-flexible but within 9-5 Eastern Time preferred. About Us: We're a tight-knit ecommerce agency with a passion for delivering exceptional online experiences, specifically within high-volume, luxury brands. Our work thrives on understanding the client's vision and bringing it to life in ways that engage and delight. We're looking for someone excited to join a dynamic team, who values attention to detail, collaboration, and quality at every turn. Role Overview: We're looking for a proactive, detail-oriented, and enthusiastic team member ready to jump-start their career in ecommerce tech. In this role, you'll have the opportunity to learn from a talented group of developers, QAs, and project managers, working closely on digital projects for a high-volume well-known fragrance brand. This is a perfect opportunity for someone who's eager to explore career paths in Project Management, eCommerce Strategy, Development, or Quality Assurance. Responsibilities: Perform comprehensive quality checks on websites, digital assets, and tools, identifying and documenting any bugs, inconsistencies, or areas for improvement. Collaborate with project managers and developers to align on client goals and project details, keeping the end-user experience top of mind. Utilize critical thinking and an investigative approach to review functionalities, ensuring each client deliverable meets our standards. Document findings, provide clear and actionable feedback, and develop test cases and guidelines as needed. Participate in training sessions, actively engaging and retaining knowledge to develop into a contributing member of the team. Support ongoing tasks, including proofreading, data entry, and other detailed-oriented work, with a commitment to accuracy. Requirements Qualifications: Bachelor's degree preferred. 1-2 years of experience in a relevant role (e.g., QA, tech support, data entry) preferred but not required. Enthusiastic about technology and curious about ecommerce, project management, development, and/or quality assurance. Strong organizational skills, attention to detail, and a “fine-toothed comb” approach to work. Excellent communication skills and a willingness to learn and grow. Ability to work independently in a remote environment, with availability during ET business hours. Benefits What We Offer: A collaborative, supportive team environment. Flexible, remote work with hours adaptable to your needs. Opportunities for growth and exposure to multiple areas of ecommerce and digital strategy. Apply Now: If you're ready to start your career in ecommerce and technology, with a passion for quality and client success, we'd love to hear from you!

. As part of one our ongoing Oracle HCM implementation, we are looking for a QA / Testing expert who can work remotely and have had previous experience in 1. Oracle Payroll testing 2. Integration Testing 3. Any experience in OIC, Oracle Integration Cloud Services is a Plus. If interested, please rush your resume, with contact details and mention your absolute best rate/hr.

Nature and Scope Reporting to the QA Compliance Program Manager, the Compliance Program Specialist II focuses on facilitating Compliance and CAPA System activities at American Regent. This is a multi-disciplinary role that will interact with all phases of production including manufacture of sterile injectables, laboratories, facilities/engineering, and materials at all American Regent Sites in Ohio. Essential Duties and Responsibilities Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. * Perform all duties in accordance with American Regent and Daiichi Sankyo Business Principles, corporate directives, SOPs, policies, and government and industry regulatory guidelines. * Responsible for executing and maintaining Internal Audit Program. Work with Functional Area Management and cross-functional teams to ensure procedural compliance and alignment with internal, regulatory, and corporate requirements. * Responsible for executing and maintaining Compliance Corrective Action and Preventive Action (CAPA) System. Work with owners and cross-functional teams to ensure appropriate Corrective Action Plans are implemented and verified for effectiveness in accordance with company SOPs, policies, and cGMPs and escalate when necessary. * Responsible for executing and maintaining Customer Complaints Program in Ohio including metric reporting. Works with functional areas to investigate and ensure timely closure of Customer Complaints. * Responsible for executing and maintaining Gap Assessment program, ensuring procedural compliance and alignment with regulatory (domestic and foreign) compendia, and corporate requirements. * Responsible for executing and maintaining inspection readiness program including participation in 'tactical room' for regulatory and customer audits. * Continually collect and maintain presentation of Quality Systems reports/metrics to Senior Management at defined frequencies. * Participate in Continuous improvement portfolio activities as it relates to Compliance. This may involve cross functionality of areas from QA, QC, OPS, and may require application of statistical concepts and methodologies. * Perform any other tasks/duties as assigned by management. Education Requirements and Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. * Bachelors in Life Science, Statistics or related field required or equivalent years of experience * Minimum of 3 years of work experience in QA, Regulatory Compliance or Pharmaceutical Operations in a cGMP manufacturing environment is required. * Experience across multiple areas including developing quality system requirements for cGMP compliance of pharmaceutical drug production and laboratory facilities, validation for pharmaceutical manufacturing facilities; review and release of cGMP production batches. * Knowledge of US regulations and established expertise in interpreting and applying to organization is required. * General knowledge of overall statistical concepts and Six Sigma Green Belt certification is preferred. American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status. Applicants have rights under Federal Employment Laws. * FMLA poster: ********************************************************** * Know Your Rights: Know Your Rights: Workplace discrimination is illegal (eeoc.gov) * Employee Polygraph Protection Act: ********************************************************* American Regent Inc. endeavors to make ********************************** accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email **************************************.

Role Description The Quality Assurance (QA) Specialist is responsible for analyzing the efficiency and effectiveness of individual case analysts. To accomplish this, the QA Specialist reviews cases, emails, and recorded telephonic interactions and evaluates them for compliance to standardized process requirements. Requirements may include soft skills in phone calls, clear communication in emails, and an adherence to directive in case work. Based on the review, the Quality Analyst provides a concise written analysis of the work reviewed along with feedback and coaching recommendations to improve the performance of the program. Required Skills and Qualifications Bachelor's Degree or equivalent OR 4 years of relevant experience in lieu of degree. Experience following defined processes. Fluent in English and Spanish Must be a US Citizen or Authorized to work in the US (if not a citizen) and a resident of the US for at least 3 years within the last 5 years. Candidates that do not meet the required qualifications will not be considered Preferred Skills & Qualifications Experience with CMS's 1095-A Advanced proficiency with MS Office including SharePoint, Teams, Excel, Word, and PowerPoint Strong verbal and written communication skills Familiarity with process improvement systems such as Lean Six Sigma, Agile, and others. Previous Federal Government experience. Disclaimers Compensation Ranges Compensation ranges for ASM Research positions vary depending on multiple factors; including but not limited to, location, skill set, level of education, certifications, client requirements, contract-specific affordability, government clearance and investigation level, and years of experience. The compensation displayed for this role is a general guideline based on these factors and is unique to each role. Monetary compensation is one component of ASM's overall compensation and benefits package for employees. EEO Requirements It is the policy of ASM that an individual's race, color, religion, sex, disability, age, sexual orientation or national origin are not and will not be considered in any personnel or management decisions. We affirm our commitment to these fundamental policies. All recruiting, hiring, training, and promoting for all job classifications is done without regard to race, color, religion, sex, disability, or age. All decisions on employment are made to abide by the principle of equal employment. Physical Requirements The physical requirements described in "Knowledge, Skills and Abilities" above are representative of those which must be met by an employee to successfully perform the primary functions of this job. (For example, "light office duties' or "lifting up to 50 pounds" or "some travel" required.) Reasonable accommodations may be made to enable individuals with qualifying disabilities, who are otherwise qualified, to perform the primary functions. Disclaimer The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to this job. Compensation Range $20.94 - $26.42 Shift Day Shift Telework Full Time Telework Travel Requirement No-Travel Not Required

We're seeking a contracted part-time Quality Assurance Specialist to assist our team on a flexible, as-needed basis. In this role, you'll review eLearning modules to ensure they meet our high standards for quality, accuracy, and functionality. This is an excellent opportunity for someone looking for part-time work with the potential for a long-term relationship. Work volume may vary, and there could be weeks without assignments, but we value reliability and consistency in our QA partners. As a Quality Assurance Specialist, you'll focus on detailed module reviews, providing feedback, and ensuring the user experience aligns with our expectations. This position is open to candidates located anywhere in the U.S. Responsibilities Review and test eLearning modules to ensure English accuracy, functionality, and alignment with design specifications. Identify and document errors or issues, including content inaccuracies, technical bugs, or usability concerns. Provide concise and clear feedback to the design and development teams. Ensure consistency in formatting, navigation, and overall user experience. Meet deadlines for reviews to support the production schedule. Compensation and Commitment Pay Rate: $10 per module (approximately 15 minutes per module). Time Commitment: Estimated 5-8 hours per week, depending on project needs. This role is part-time and as-needed, meaning workloads may vary, and there may be weeks or months with no assignments. Preferred Qualifications Strong command of written and spoken English, with excellent grammar, spelling, and proofreading skills. Prior experience in quality assurance, testing, or a similar role (eLearning or digital content QA is a plus). Familiarity with eLearning platforms and tools is a bonus but not required. Strong attention to detail and a commitment to delivering high-quality work.Ability to work independently and communicate feedback effectively. Skills and Abilities Excellent problem-solving and analytical skills. Strong written communication skills for documenting issues clearly. Ability to manage time effectively and prioritize tasks to meet deadlines. Reliability and consistency in delivering results. If you're detail-oriented, flexible, and excited about contributing to a team dedicated to creating exceptional learning experiences, we'd love to hear from you!