quality assurance associate

Domino's

<p><b>Position: </b>Quality Assurance Associate Manager</p><p><b>Location: </b>Karachi</p><p><b>Role Overview:</b></p><p>To supervise and verify the Quality Assurance processes Dominos Stores as per DPI and Local Authorities Guidelines.<br/>Contribute to new business initiatives and projects and review and communicate the impact on Quality activities.</p><p><b>Key Responsibilities: </b></p><p>Expansion of testing and monitoring procedures of product quality of domino&rsquo;s pizza outlets.<br/>Creating, reviewing, and testing technical specifications documents and effective testing plans and test cases.<br/>Visiting Supplier&rsquo;s Facility for Continual Improvement on Food Safety Standards.<br/>Assist directly to Manager Quality during all the External Audits at all Regions as per DPI guidelines.<br/>Conduct Food safety and NSF guideline related trainings to all region for stores and Commissaries.</p><p><b>Required Skills and Competencies:</b></p><p>Knowledge of food safety standards.</p><p>Can conduct FS audits individually.</p><p>Have a sound knowledge of Food safety certifications.</p><p>Can travel alone.</p><p>Basic knowledge about third party audits at stores.</p><p>Responsible AND reliable in actions.</p><p><b>Experience: </b>4 to 5 Years</p><p><b>Qualification: </b>Bachelor's Degree in Food Science/Technology</p><p>Job Type: Full-time</p><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Work Location: In person</p>

Quality Assurance Associate Manager

Minerva Research Solutions

<div><p><b>JOB DESCRIPTION:</b><br>
<br>
Minerva Research Solutions is a clinical trial management service provider. We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle.</p><p>
Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines &amp; real-time solutions. Our clinical trial support services &amp; consultations are tailored to foster your product and requirements.<br>
<br>
We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process.<br>
<br>
Minerva Research Solution is looking for dynamic individuals with a passion for ensuring the highest standards in clinical trial data quality assurance. As a key player in our team, you will play a crucial role in maintaining the integrity and accuracy of clinical trial data.</p><p><b>
Responsibilities:</b></p><ul><li>
Perform comprehensive data-driven Quality Monitoring activities to ensure compliance with regulatory requirements and SOPs, and to ensure a continued state of inspection readiness.</li><li>
Ensure data is recorded under sponsor protocol, GCP guidelines, industry guidelines, and agency regulations.</li><li>
Perform quality control checks; identify and track source documentation errors and non-conformances with requirements.</li><li>
Provide ongoing compliance support including but not limited to:</li><li>
Preparing periodic clinical trial quality reports for assigned programs and assessing these reports with applicable clinical team members to identify areas of risk. Collaborates with applicable team members to develop risk mitigation plans.</li><li>
Collaborating with the Clinical Team to share audit/inspection observations for lessons learned across protocol, and/or program, and working with appropriate groups to implement Corrective Action Plans (CAPAs).</li><li>
Performs quality reviews of key documents developed for use in clinical trials and in preparation for submission to regulatory health authorities.</li><li>
Assist in preparing for all Sponsor and FDA audits.</li><li>
Assist in conducting internal audits to review key processes.</li><li>
Provide appropriate support to assigned cross-functional workgroups.</li><li>
Establishes effective partnerships with internal staff to facilitate the timely identification and resolution of compliance and quality matters and other opportunities for quality process improvement.</li><li>
Query resolution and data entry and questionnaire preparation regarding the respective studies.</li><li>
Other related Quality Assurance projects as assigned.</li><li>
The QA Associate will report to the Quality Assurance Lead</li></ul><p><b>
Knowledge, Education, and Experience:</b></p><ul><li>
Qualified Profession with strong medical background (Pharm-D, MBBS, BDS etc) with a keen interest in Clinical Research are strongly encouraged to apply.</li><li>
In-depth knowledge of FDA, GCP, ICH, and other state and federal agency guidelines for the conduct of clinical trials.</li><li>
Knowledge of IRB requirements.</li><li>
1+ years in work related to Quality Control / Quality Assurance area in clinical research will preferred..</li><li>
Experience including external clinical/regulatory and document auditing will be a plus</li></ul><p><b>
Skills and Abilities:</b></p><ul><li>
Good communication skills (interpersonal, written, verbal)</li><li>
Strong attention to detail and good time management skills</li><li>
Flexible attitude concerning work assignments</li><li>
Ability to manage multiple and varied tasks in a fast-moving environment</li><li>
Ability to interact professionally at all levels within the organization.</li><li>
Knowledge of the HIPAA Privacy Act and its application to clinical research.</li></ul><b>
Benefits:</b><ul><li>
Competitive salary and performance-based bonuses.</li><li>
Medical health insurance coverage.</li><li>
Employees Old-age benefits coverage.</li><li>
Flexible work hours and remote work options.</li><li>
Professional learning and development support.</li><li>
Generous vacation and paid time off.</li><li>
Employee assistance programs for mental health.</li><li>
Company-sponsored events and team-building activities.</li><li>
Diverse, professional, and inclusive work environment.</li><li>
Opportunities for career growth.</li><li>
Cutting-edge technology and tools.</li><li>
Family-friendly policies, including parental leave.</li><li>
Commuter benefits or transportation assistance.</li><li>
Social responsibility and community involvement programs.</li></ul><b>
Openings:</b><p>
04 positions<br>
Full-time<br>
On-site job<br>
<br>
<b>Work Schedule Timings:</b><br>
Monday to Friday<br>
Evening Shift (07 PM to 03 AM)<br>
(transport facility provided for female staff only and allowance for male employees, additional night shift allowance)</p><p>
</p><p>vapSso9DaM</p></div>

Clinical Trials Quality Assurance Associate (Night)

Cipla Ltd

<div><div><b>NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates.</b></div><br>
<div>
</div><div><b>Job Title</b>: Analytical QA Associate III</div>
<div><b>
FLSA Classification</b>: Professional, Exempt
</div><div><b>Work Location</b>: Central Islip, NY
</div><div><b>Work Hours:</b> General: 8:30AM &ndash; 5:00PM (may vary based on business needs)</div>
<div><b>
Reports To</b>: Supervisor or Manager</div>
<p><b>
Salay Range:</b> $72,800 - $93,600</p><br>
<p></p>
<p><b>
Purpose: </b>This position requires a strong analytical chemistry/lab background and experience. The job duties for this position include but are not limited to the following:</p>
<p><b>
Scope</b>:
</p><div>The Analytical Quality Assurance (AQA) associate III position is an team or individual contributor role and reports to the Supervisor Analytical Quality Assurance for InvaGen Pharmaceuticals, Inc., a Cipla subsidiary located at Hauppauge, NY.
</div><div><b>The job duties for this position include but are not limited to the following</b>:</div>
<ul>
<li>Reviewing and confirming the compliance related to raw materials, inprocess and finished product analytical documents.</li>
<li>Monitoring and ensuring of current Good Laboratory Practices (cGLP) followed by laboratory personnel during routine operation to ensure adherence to procedure.</li>
<li>Confirming and ensuring compliance of the protocols and reports of method validations / verifications / comparison reports and any other study reports.</li>
<li>Prepare and review laboratory investigation (OOS/OOT/Deviation) reports and ensure compliance of same.</li>
<li>Verifying the laboratory chemicals/reagents, standards for completeness of the labels against standard operating procedures (SOPs).</li>
<li>Assessing and implementing Pharmacopoeia changes whenever any new edition, supplement, amendment, or other changes of any Pharmacopoeia are in effect.</li>
<li>Review of laboratory audit trials during data review against standard operating procedures (SOPs).</li>
<li>Coordinating with the Analytical Laboratory Teams to arrange required documents to cross functional teams.</li>
<li>Maintaining all the incoming documents with proper tracking, recording, storage and archival of the documents.</li>
<li>Reviewing and identifying the gaps within the system during routine monitoring and informing the supervisor of necessary improvements in the identified areas.</li>
<li>Actively participating in review of data related to laboratory investigations and incidents and ensuring proper compliance.</li>
<li>Performing other departmental and cross-functional projects and assignments given by the manager/supervisor.</li></ul><br>
<div></div>
<p><b>
Education and Experience</b></p>
<ul>
<li>Possess a minimum bachelor&rsquo;s degree in chemistry, Pharmaceutical Sciences, or related field of study from an accredited institution. Master&rsquo;s degree in the above and/or related fields of study as noted above preferred.</li>
<li>A minimum of 5-8 years in analytical (preferably in analytical quality assurance for minimum 3years).</li>
<li>Must be proficient in computer skills and software applications such as Microsoft Office tools and Quality applications and software programs.</li>
</ul><ul><li>Strong knowledge and experience with analytical laboratory activities in areas such as active pharmaceutical ingredients (API), drug products, analytical development, Quality Control (QC), Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP)/Good documentation Practices (GDP), USP monograph requirements.</li></ul><br>
<div></div>
<p><b>
Technical Knowledge and Computer Systems Skills</b>
</p><ul><li>Understanding of laboratory equipment operation, qualification and calibrations which includes their software audit trial reviews. E.g. HPLC, UV Vis Spectrophotometer, GC, Potentiometer, pH meter, Stability chambers, etc.</li>
<li>Strong knowledge on USP monograph requirements, FDA &amp; ICH guidance requirements, etc.</li>
<li>Effective interpersonal relationship skills and the ability to work in a team environment.</li>
<li>Experience in Inhalation products (MDI) is a plus.</li>
</ul><ul><li>Ability to work in a fast-paced, dynamic environment within a manufacturing operation setting.</li>
<li>Must be able to communicate clearly and concisely across all levels of the organization and possess a solid command of English language communication skills verbally, written, and interpersonally.</li>
<li>Must possess strong documentation and technical writing skills, and able to apply relevant scientific principles and practices.</li>
<li>Must be able to work under minimal supervision and able to work independently and in a team environment.</li>
</ul>
<p><b>Professional and Behavioral Competencies</b></p>
<ul>
<li>Proficiently speak English as a first or second language and ability to read, write and communicate effectively the same.</li>
<li>Must be a self-starter and demonstrate initiative to seek additional training or direction as needed.</li>
<li>Must be willing and able to work any assigned shift ranging from first or second shift; work schedules may be Monday to Friday.</li>
</ul><ul><li>Knowledge of good manufacturing practices and good documentation practices preferred.</li>
<li>Self-motivated, with the ability to work in a fast-paced manufacturing environment and handle multiple tasks simultaneously.</li>
<li>Excellent organizational skills with the ability to focus on details.</li>
</ul>
<div><b>Work Schedule and Other Position Information</b>:
</div><ul><li>General shift but must be willing and able to work any assigned first or second shift. Work schedule may be Monday to Friday, Tuesday to Saturday, or some combination thereof based on business needs.</li>
<li>Must be willing to work some weekends based on business needs as required by management.
</li><li>Relocation negotiable.</li>
<li>No remote work available.</li>
<li>This role works in cGMP laboratory or manufacturing environment, where personal protective equipment (PPEs) is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc.</li>
<li>The role may be assigned on a work-shift basis where required (Day, Evening, Night). Weekend or Holiday work may be requested or required based on business needs.</li></ul><br>
<div></div>
<p><b>
GLOBAL COMPANY</b></p>
<p>
Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India&rsquo;s pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.</p>
<p>
Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla&rsquo;s focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.</p><br>
<p></p>
<p><b>
CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.)</b></p>
<p>
About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited.</p></div><p></p>

Analytical QA Associate III

Pearson

<div><p>Content Quality Assurance &ndash; Accessibility</p>
<p>Role: Content Quality Assurance</p>
<p>Tier: IC15</p>
<p>Job Family: Learning &amp; Content Development</p>
<p>Job Category: Content Creation</p>
<p>Track: Individual Contributor</p>
<p>Level: Level 1 - Associate Professional</p>
<p>Accessibility QA Qualifications:</p>
<ul><li>Proven ability to perform hands on Accessibility testing using various assistive technologies.</li>
<li>Expert knowledge of WCAG guidelines and success criteria for proper testing and reporting outcomes.</li>
<li>Capable and motivated to coordinate with Developer &amp; Engineering teams, to provide support and code level advice to resolve issues.</li>
<li>Critical thinker, able to perform data driven analysis for triaging complex issues, designing solutions, and supporting fix implementation.</li>
<li>Ability to validate accuracy of reporting performance on work performed by other teammates, and providing feedback for improvement.</li>
<li>Collaborative and eager to learn and share knowledge.</li>
<li>Certifications desired CPACC, WAS, or CPWA</li>
</ul><p>ROLE SUMMARY</p>
<p>The advanced associate carries out quality assurance reviews with a greater degree of independence, evaluating more detailed aspects of content such as clarity, functionality of digital assets, and alignment with expected standards. This role supports content projects by resolving routine issues, recommending corrections to content teams, and maintaining clear records of findings. The individual collaborates across functions to ensure timely progress and has some autonomy in troubleshooting straightforward content discrepancies, escalating complex concerns as necessary.</p>
<p>KEY PERFORMANCE INDICATORS</p>
<p>High completion rate of assigned content checks demonstrated attention to detail when applying QA standards to varied formats, and thorough recording of outcomes in project documentation represent success at this tier. The associate contributes to timely project delivery by identifying recurring defects and ensuring reviewed materials consistently meet minimum quality thresholds.</p>
<p>BEHAVIORAL EXPECTATIONS</p>
<p>Customer Centricity is shown by considering how content quality impacts end-users. Raising the Performance Bar appears through actively seeking out areas to enhance review processes. Exceptional Collaboration for Value is evident when coordinating findings with team members, while Our Leaders Inspire can be seen in embracing mentorship and knowledge sharing during daily work.</p>
<p><b>Who we are:</b></p>
<p>At Pearson, our purpose is simple: to help people realize the life they imagine through learning. We believe that every learning opportunity is a chance for a personal breakthrough. We are the world's lifelong learning company. For us, learning isn't just what we do. It's who we are. To learn more: We are Pearson.</p>
<p>Pearson is an Equal Opportunity Employer and a member of E-Verify. Employment decisions are based on qualifications, merit and business need. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, sexual orientation, gender identity, gender expression, age, national origin, protected veteran status, disability status or any other group protected by law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.</p>
<p>If you are an individual with a disability and are unable or limited in your ability to use or access our career site as a result of your disability, you may request reasonable accommodations by emailing TalentExperienceGlobalTeam@grp.pearson.com.</p>
<p><b>Job:</b> Content Creation</p>
<p><b>Job Family:</b> LEARNING\<i>&amp;\</i>CONTENT\_DEVELOPMENT</p>
<p><b>Organization:</b> Higher Education</p>
<p><b>Schedule:</b> FULL\_TIME</p>
<p><b>Workplace Type:</b> Hybrid</p>
<p><b>Req ID:</b> 21483</p>
<p>\#LI-REMOTE</p></div><p></p>

Content Quality Assurance

<div><div><p><b>Vacancy Name</b></p><div> Associate Quality Assurance Analyst</div></div><br>
<div><p><b>
Requisition No</b></p><div> VN4110</div></div><br>
<div><p><b>
Time Type</b></p><div> Full Time</div></div><br>
<div><p><b>
Location</b></p><div> Gurgaon Office</div></div><br>
<div><p><b>
Additional Location</b></p></div><br>
<div></div><div><p><b>
Country</b></p><div> India</div></div><br>
<div><p><b>
Job Description</b></p><div><div><div><b>
Find purpose in each day while contributing to a workplace revolution! SHL, People Science. People Answers.</b><br>
<br>
Would you like to provide support to some of the largest businesses globally utilizing the SHL&rsquo;s extensive suite of Assessments and Platforms? If so, perhaps you would like to develop your experience within a world renowned, fast-growing HR SaaS organization as an <b>Associate Quality Assurance Analyst</b>? SHL works with some of the world&rsquo;s most prestigious companies who believe us to revolutionize their workplaces and help them to thrive and you can become a part of this.<br>
A great benefits package is offered in a culture where career development, with ongoing manager guidance, collaboration, flexibility, diversity, and inclusivity are all intrinsic to our culture. There is a huge investment in SHL currently so there&rsquo;s no better time to become a part of something transformational.<br>
<br>
<b> </b><b>What you will be doing:</b>
<ul><li>Work with cross-functional teams to ensure quality throughout the software development lifecycle</li><li>
Analyze data to identify areas for improvement in the quality system</li><li>
Assure ongoing compliance with quality and industry regulatory requirements</li><li>
Writing and reviewing testing plans</li><li>
Investigating causes of defects that occur during the testing phase</li><li>
Inspection of products is part of the job with the obligation to report and document findings.</li></ul>
<br>
<b>What we are looking for from you:</b><br>
Essential:
<ul><li>Basic SQL and JIRA knowledge</li><li>
Strong Microsoft Office knowledge</li><li>
Manual Testing</li></ul>
<br>
Desirable:
<ul><li>Business level English language</li><li>
Analytical skills</li></ul>
<b>Get in touch:</b><br>
Find out how this one-off opportunity can help you to achieve your career goals by making an application to our knowledgeable Talent Acquisition team. Choose a new path with SHL.</div></div><br>
</div></div><br>
<div><p><b>
About Us</b></p><div><div><div><ul><li>
We unlock the possibilities of businesses through the power of people, science and technology.</li><li>
We started this industry of people insight more than 40 years ago and continue to lead the market with powerhouse product launches, ground-breaking science and business transformation.</li><li>
When you inspire and transform people&rsquo;s lives, you will experience the greatest business outcomes possible. SHL&rsquo;s products insights, experiences, and services can help achieve growth at scale.</li></ul></div></div><br>
</div></div><br>
<div><p><b>
What SHL can offer you</b></p><div><div><div><p>
Diversity, equity, inclusion and accessibility are key threads in the fabric of SHL&rsquo;s business and culture (find out more about DEI and accessibility at SHL)</p>
<ul><li>Employee benefits package that takes care of you and your family.</li><li>
Support, coaching, and on-the-job development to achieve career success</li><li>
A fun and flexible workplace where you&rsquo;ll be inspired to do your best work (find out more LifeAtSHL)</li><li>
The ability to transform workplaces around the world for others.</li></ul>
<p>SHL is an equal opportunity employer. We support and encourage applications from a diverse range of candidates. We can, and do make adjustments to make sure our recruitment process is as inclusive as possible.</p></div></div></div></div></div>

Associate Quality Assurance Analyst

Hul Hub Pvt Ltd

<p>Associate SQA Engineer<b>Job Description:</b></p><ul><li>Develop, document, and execute manual test cases based on software requirements and specifications.</li><li>Perform functional, regression, integration, and user acceptance testing (UAT) to ensure the software performs as expected.</li><li>Work closely with developers, business analysts, and other team members to clarify test requirements and ensure proper test coverage.</li><li>Reproduce, debug, and isolate issues for resolution by the development team.</li><li>Participate in requirements and design reviews to understand the expected behavior of the software.</li><li>Verify bug fixes and assist in retesting of resolved issues.</li></ul><p><b>Qualifications:</b></p><ul><li>Bachelor&rsquo;s degree in Computer Science,</li></ul><p><b>Job Specifications:</b></p><ul><li>0-6 months of experience in manual software quality assurance or testing.</li><li>Experience with testing web-based applications.</li><li>Basic knowledge of SQL for verifying data in databases.</li><li>Understanding of the SDLC/STLC and QA processes.</li><li>Familiarity with web technologies (e.g., HTML, JavaScript, and APIs) is a plus.</li></ul><p><b>Perks &amp; Benefits:</b></p><ul><li>Market competitive salary package</li><li>Career growth opportunities</li><li>Health care benefits</li><li>Provident Fund &amp; EOBI</li><li>Subsidized Transport facility (subject to availability)</li></ul><p><b>Location:</b></p><p>Karachi, Sindh - Pakistan</p><p>Job Types: Full-time, Fresher</p><p>Pay: Rs55,000.00 - Rs60,000.00 per month</p><p>Work Location: In person</p>

Associate SQA Engineer

Lumos Pharma, Inc.

<div><div><b>Clinical Quality Assurance Specialist</b></div>
<div></div><div>Lumos Pharma is a clinical-stage biopharmaceutical company whose mission is to develop new therapies for people with rare diseases, prioritizing its focus where the medical need is high, and the pathophysiology is clear. We are committed to this mission and a strategy grounded upon time and cost-efficient drug development to deliver safe and effective therapies to patients. We take a patient-centric approach and maintain inspection-readiness across our programs.</div>
<div></div><div>This position reports to the Vice President, Quality and Compliance, and is responsible for providing quality oversight of clinical trial activities performed in compliance with Good Clinical Practices (GCP). This position also supports internal quality systems and compliance functions. The Clinical Quality Assurance Specialist is expected to execute established processes involving quality assurance, quality systems, and compliance.</div>
<div></div><div>ESSENTIAL FUNCTIONS</div>
<ul><li>Author, review, and/or approve SOPs, protocols, study plans, and other applicable clinical documents in accordance with GCP requirements</li>
<li>Provide input on protocol deviations and associated corrective/preventive actions involving clinical trials.</li>
<li>Perform audits of clinical trial sites and clinical studies (e.g., trial master file, clinical study report, etc.)</li>
<li>Complete required tasks in the electronic quality management system</li>
<li>Assist with training coordination, ensuring employees are up to date on quality and compliance requirements</li>
<li>Assist with audits of external suppliers</li>
<li>Routinely work with internal and external stakeholders to achieve cross-functional goals.</li>
<li>Each employee is responsible for financial and compliance controls as they relate to their roles. For example, being fiscally responsible in purchasing decisions and completing compliance training within the specified time frames.</li>
</ul><div><div><div>REQUIRED QUALIFICATIONS</div>
<div></div><div>Education</div>
<ul><li>Bachelor's Degree (four-year college or technical school) required, Field of Study: Biology, Chemistry, Health Administration, or related technical discipline</li>
</ul><div>EXPERIENCE</div>
<ul><li>1-3 years of experience in quality assurance within the pharmaceutical or biotech industry</li>
</ul>
<div></div><div>PREFERRED QUALIFICATIONS</div>
<ul><li>Knowledge of GMP and GCP regulations</li>
<li>Strong attention to detail, documentation accuracy, and organizational skills</li>
<li>Microsoft Office</li>
<li>Experience with MasterControl is desirable</li>
<li>Experience with CDER BIMO inspections is desirable</li>
</ul>
<div></div><div>COMPETENCIES</div>
<ul><li>Analytical Skills: Strong analytical skills with a strategic mindset for clinical development and commercialization.</li>
<li>Communication: Excellent communication skills, with the ability to clearly articulate complex scientific information to technical and non-technical audiences.</li>
<li>Relationship Builder: Ability to work effectively in a cross-functional team environment and to build relationships with internal and external stakeholders.</li>
<li>Business Acumen: Business acumen is the ability to understand and discriminate between various business-related topics and issues.</li>
<li>Decision-Making/Judgment: Decision-making skills look at the ability of the individual to select an effective course of action while controlling resources and expenditures.</li>
</ul>
<div></div><div>WORK ENVIRONMENT</div>
<div>This position can work remotely in the United States.</div>
<div></div><div>TRAVEL EXPECTATION</div>
<div>Up to 10%</div>
<div></div><div>What you can expect as a Lumosian</div>
<ul><li>Industry-competitive compensation</li>
<li>Generous health and welfare benefits, including company-paid dental and vision benefits with dependents coverage, short-term and long-term disability, and basic life Insurance.</li>
<li>Lumos covers 85 &ndash; 95% of the medical premium</li>
<li>Health Reimbursement Arrangement</li>
<li>8 weeks of fully paid parental leave for all new parents</li>
<li>Gym or fitness class reimbursement</li>
<li>401(k) with 5% employer contribution</li>
<li>Flexible work hours and location</li>
<li>Generous PTO policy</li>
<li>11 paid holidays in the US</li>
<li>Offices in Austin, TX, and Ames, IA</li></ul></div></div></div><div></div>

Clinical Quality Assurance Specialist

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