software quality assurance specialist

VITROLIFE

<div>At the Vitrolife Group, we work every day to unlock the full potential of science and technology to reduce the barriers towards building a family. Together we help our customers and their patients to fulfill the dream of having a baby. 
Make Quality Matter &mdash; Where It Impacts Lives.
We are looking for a Quality Assurance Specialist to strengthen and advance our local quality operations in Riyadh. This role sits at the intersection of regulatory excellence, operational quality, and continuous improvement, ensuring that our laboratory services meet the highest international and local standards.
You will play a key role in driving compliance, enabling safe and effective services, and embedding a proactive quality culture &mdash; working closely with both local teams and regional quality leadership.<h4 class="jobSectionHeader"> 
Your Impact</h4>
As a Quality Assurance Specialist, you will:<h6 class="jobSectionHeader">
Drive Quality Operations &amp; Compliance</h6><ul><li>
Oversee day-to-day quality activities and ensure adherence to local and regional requirements</li><li>
Maintain accurate quality records and actively participate in quality management forums</li><li>
Ensure compliance with MOH, SFDA, CBAHI, and other applicable regulations</li></ul><h6 class="jobSectionHeader">
Strengthen the Quality Management System (QMS)</h6><ul><li>
Manage document control processes to ensure procedures are current, compliant, and accessible</li><li>
Support implementation and updates of local and global procedures</li><li>
Contribute to continuous improvement of QMS processes</li></ul><h6 class="jobSectionHeader">
Lead Audits, Risk &amp; Continuous Improvement</h6><ul><li>
Plan and conduct internal audits; manage findings and CAPA implementation</li><li>
Support external audits and regulatory inspections</li><li>
Lead local risk assessments and foster a proactive risk management culture</li></ul><h6 class="jobSectionHeader">
Manage Deviations, CAPA &amp; Performance</h6><ul><li>
Investigate deviations and ensure effective CAPA closure</li><li>
Monitor KPIs, incidents, and nonconformities</li><li>
Identify trends and escalate critical insights to Regional Quality Management</li></ul><h6 class="jobSectionHeader">
Enable Regulatory &amp; Operational Excellence</h6><ul><li>
Monitor regulatory changes and ensure timely implementation</li><li>
Support licensing, certifications, and renewals</li><li>
Ensure quality alignment in new or modified services</li></ul><h6 class="jobSectionHeader">
Collaborate &amp; Build Capability</h6><ul><li>
Train and support staff on quality and regulatory requirements</li><li>
Evaluate the external critical suppliers/service provider and referral laboratories to ensure compliance</li><li>
Contribute to regional and global quality initiatives and harmonization efforts</li></ul><h4 class="jobSectionHeader">
Who You Are</h4>
You are a structured, analytical, and proactive quality professional who thrives in regulated environments and enjoys collaborating across teams.<h4 class="jobSectionHeader">
Qualifications</h4><ul><li>
Bachelor&rsquo;s degree in Laboratory Sciences, Biomedical Sciences, or related field</li><li>
SCFHS license (preferred)</li><li>
Certification in Quality Assurance or Regulatory Affairs is a plus</li></ul><h4 class="jobSectionHeader">
Experience</h4><ul><li>
3&ndash;4 years in a similar QA/regulatory role</li><li>
Experience within laboratory or medical environment</li><li>
Strong knowledge of:<ul><li>
MOH and SFDA regulations (required)</li><li>
CBAHI standards (required)</li><li>
ISO 15189 and CAP accreditation (preferred)</li></ul></li></ul><h4 class="jobSectionHeader">
Skills</h4><ul><li>
Strong understanding of QMS, audits, and documentation</li><li>
Experience with QMS/LIS systems</li><li>
Excellent problem-solving and organizational skills</li><li>
Strong communication and collaboration abilities</li><li>
Fluent in Arabic and English (written and spoken)</li></ul><h4 class="jobSectionHeader">
What You Bring Beyond the Basics</h4><ul><li>
A proactive mindset &mdash; you don&rsquo;t wait for issues, you prevent them</li><li>
The ability to translate regulations into practical, working processes</li><li>
Confidence to challenge, improve, and influence</li><li>
A strong sense of ownership and accountability</li></ul><h4 class="jobSectionHeader">
Why Join Us</h4><ul><li>
Be part of an organization where quality is central to patient impact</li><li>
Work in a collaborative regional and global environment</li><li>
Contribute to high-standard laboratory services and continuous improvement</li><li>
Grow within a culture that values expertise, structure, and innovation</li></ul><h6 class="jobSectionHeader">
Additional Information</h6><ul><li>
Preference will be given to Saudi Nationals</li></ul>
Vitrolife Group is a global provider of medical devices and genetic services. Based on science and advanced research capabilities, we develop services and products for personalized genetic information and medical device products. We support our customers by improving their clinical practice for the patient's outcome of fertility treatment.
We are currently approximately 1 100 colleagues worldwide, with headquarters in Gothenburg, Sweden. Vitrolife Group's products and services are available in more than 110 countries through our own presence in 30 countries and a network of distributors. Vitrolife Group is a sustainable market leader and aims to be the preferred partner for IVF-clinics by providing superior products and services with the vision of fulfilling the dream of having a baby. The Vitrolife share is listed on Nasdaq Stockholm.</div>

Quality Assurance Specialist

Arrivy Inc.

Who is Arrivy?Arrivy is the place to do something bigger than yourself. We are a fast-growing software product company based in the US with deep product roots in Pakistan.Arrivy offers an operational solution for service businesses looking to streamline their workflow with simple yet effective means. Over the years, we have formed strong connections with our customers through persistent hard work &amp; passion.We are looking for someone ambitious and self-motivated who can work to expand our customer base by running our outbound email marketing campaign. Our team comprises operations and logistics veterans from Microsoft, eBay, Autodesk, and Adobe. The opportunities to learn would be endless. If you're looking to become a powerhouse, Arrivy is just the place to be.Your Duties for a Typical Day:As an Outbound Sales Specialist you&rsquo;ll need to:<ul><li>Review requirements, specifications and technical design documents to provide timely and meaningful feedback</li><li>Create detailed, comprehensive and well-structured test plans and test cases</li><li>Estimate, prioritize, plan and coordinate testing activities</li><li>Identify, record, document thoroughly and track bugs</li><li>Perform thorough regression testing when bugs are resolved</li><li>Develop and apply testing processes for new and existing products to meet client needs</li><li>Liaise with internal teams (e.g. developers and product managers) to identify system requirements</li><li>Monitor debugging process results</li><li>Investigate the causes of non-conforming functionality/release and train users to implement solutions</li><li>Track quality assurance metrics, like defect densities and open defect counts</li><li>Stay up-to-date with new testing tools and test strategies</li></ul>Experience &amp; Other Skills:You'll need to have:<ul><li>Strong knowledge of software QA methodologies, tools and processes</li><li>Experience in writing clear, concise and comprehensive test plans and test cases</li><li>Hands-on experience with both white box and black box testing</li><li>Experience working in an Agile/Scrum development process</li><li>Experience with performance and/or security testing is a plus</li></ul>What Does Arrivy Offer You?<ul><li>Highly competitive salaries</li><li>Talented, passionate, and fun colleagues</li><li>International working exposure</li><li>Learning and growth opportunities</li><li>Performance-based Incentives and bonus plan</li><li>Team building activities</li></ul>Job Type: Full-timePay: Rs60,000.00 - Rs150,000.00 per monthWork Location: In person

Software Quality Assurance Engineer

State of South Carolina

<div>
 
 Job Responsibilities
 
 
 
 The mission of the SC Commission for the Blind (SCCB), established in 1966, is to provide quality individualized vocational rehabilitation services, independent living services, and prevention-of-blindness services to South Carolinians who are blind or low vision leading to competitive employment and social and economic independence. Our goal is to become a national model vocational rehabilitation agency for people who are blind or low vision, demonstrating quality services, accountability, innovation, effectiveness and efficiency.
 
 
 Do you want a career doing meaningful work that has a positive impact on people's lives? Have you thought about a career in state government but weren't sure how or where to begin? The SCCB is looking for hard working passionate individuals such as you! Every SCCB employee is important and a career with the SCCB will give you the opportunity to grow professionally and personally as you play a crucial role in the delivery of services to South Carolinians with visual impairments.
 
 
 
 Duties
 
 
 
 We are seeking a passionate and knowledgeable person to perform fiscal and programmatic quality assurance duties to assess compliance, performance, and customer service. This role includes conducting quality case reviews and administering consumer surveys to evaluate service effectiveness and identify areas for improvement. The Specialist exercises strong knowledge of federal regulations, Consumer Services Policy, and the agency&rsquo;s Fees, Codes and Procedures policy to communicate compliance findings clearly and effectively. Duties will include:
 
 
 <ul>
 <li>
 Review authorization for appropriate documentation, fees, codes, forms, and compliance with Federal and state regulations, and Consumer Services policies and procedures; issue authorizations and communicate with originating staff members within 5 business days of receipt.
 </li>
 <li>
 Initiate the planning, coordinating, and conducting of Quality Assurance Reviews on a daily basis to assess the agency's program integrity in the areas of compliance and quality service delivery.
 </li>
 <li>
 Conducts consumer surveys across all agency programs and maintains reports to track feedback, trends, and areas for improvement.
 </li>
 <li>
 Identify trends, both positive and negative, resulting from the fiscal compliance QA reviews and programmatic compliance reviews that can be used to train or clarify policy or procedures for staff and improve accuracy of requests and service delivery.
 </li>
 <li>
 Conduct special topical reviews as directed by the Quality Assurance Director to identify compliance issues and other areas of service delivery or caseload management in need of improvement.
 </li>
 <li>
 Assist in the ongoing activities of the Quality Assurance Division to ensure that individual, area, and statewide compliance occurs as outlined by agency and federal regulations.
 </li>
 <li>
 Other duties as assigned.
 
 
 </li>
 </ul>
 
 Minimum And Additional Requirements
 
 
 
 A high school diploma and experience in business management, public administration, or administrative services. A bachelor's degree may be substituted for the required work experience.
 
 
 
 Additional Requirements
 
 
 
 Knowledge of agency's mission, programs and objectives. Ability to exercise and exhibit a strong knowledge of federal regulations, Consumer Services policy and procedure, agency's fees, and codes in order to efficiently and clearly communicate compliance findings to the requestor. Ability to review payments against authorization for appropriate processing by field staff.
 
 
 
 Additional Comments
 
 
 
 
 The SCCB is committed to providing equal employment opportunities to all applicants and does not discriminate on the basis of race, color, religion, sex (including pregnancy, childbirth, or related medical conditions including, but not limited to, lactation), national origin, age (40 or older), disability or genetic information.
 
 
 
 The SCCB offers an exceptional benefits package for full time (FTE) employees:
 
 
 <ul>
 <li>
 Health, dental, vision, long-term disability, and life insurance for employees, spouses, and children,
 </li>
 <li>
 15 days of annual (vacation) leave per year*,
 </li>
 <li>
 15 days of sick leave per year,
 </li>
 <li>
 13 paid holidays,
 </li>
 <li>
 Paid Parental Leave,
 </li>
 <li>
 Relocation reimbursement**,
 </li>
 <li>
 State Retirement Plan and Deferred Compensation Programs, and
 </li>
 <li>
 Public Service Loan Forgiveness.
 </li>
 <li>
 Employees holding FTE status earn additional annual leave the longer they remain employed with the state.
 </li>
 <li>
 Eligible new hires from out-of-state may receive up to $5,000 in reimbursements for certain expenses, pursuant to Section 8-11-135 of the South Carolina Code of Laws.
 
 
 </li>
 </ul>
 
 A copy of your transcript may be uploaded as an attachment to the application. Upon hiring, candidates must submit official college transcript(s) or diploma(s) for degree(s) obtained. Failure to produce an official, certified transcript may result in not being hired or termination.
 
</div>

Quality Assurance Specialist - 60026087

AT&T

<div>This position requires office presence of a minimum of 5 days per week and is only located in the location(s) posted.
AT&amp;T Global Public Sector is a trusted provider of secure, IP enabled, cloud-based, network solutions and professional services to the Federal Government. We are dedicated to recruiting, developing and empowering a diverse, high-performing workforce that is passionate about what they do, committed to our shared values and dedicated to our customers&rsquo; mission.
AT&amp;T provides professional services to the office of the Marine Corps' Assistant Deputy Commandant for Installations &amp; Logistics (I&amp;L), Logistics Plans, Policies and Strategic Mobility. Work includes Strategic Communications Management, Logistics Innovation &amp; Advocacy, IT Portfolio Management, Data Management, Analytics, Program Management and other related services in order to improve and enhance the lethality of the Marine Air/Ground Task Force (MAGTF) through logistics speed, agility, and flexibility.
AT&amp;T has an opening for a Quality Assurance Specialist to support DoD and federal defense customers by leading and directing complex projects, serving as the primary liaison to clients, and ensuring delivery of program objectives within budget, schedule, and compliance requirements in a mission-driven government environment.
Job Duties/Responsibilities:<ul><li>
Performs quality assurance review on deliverables, projects, documents, products, etc. and provides feedback.</li></ul>
What You&rsquo;ll Need<ul><li>
Demonstrated experience performing duties within a DoD, federal, or defense‑support environment</li><li>
Ability to operate effectively in a structured, mission‑driven, and customer‑facing government setting</li><li>
Experience supporting programs with defined task orders, performance metrics, and delivery timelines</li><li>
Ability to comply with all federal government contracting, suitability, and security requirements</li><li>
Strong communication skills and the ability to work with military, civilian, and contractor personnel</li></ul><div>
Required Clearance:
Must be a US Citizen and able to attain clearance.
CLEARABLE; SECRET PREFERRED (clearable) (#secret)
Required Qualifications:<ul><li>
8+ years of experience</li><li>
Prior experience supporting USMC, DoD, or other federal defense organizations</li><li>
Familiarity with Marine Corps organizational structures, operational processes, or logistics/IT environments</li><li>
Experience briefing or supporting senior government or military leadership</li><li>
Understanding of federal acquisition, compliance, or operational frameworks</li></ul>
This position requires the ability to obtain and maintain a government security clearance at the level required by the task order. Employment is contingent upon successful completion of the security clearance process and continued eligibility throughout the course of employment.<div>
Our Quality Assurance Specialist's earn between $104,418 -$114,746. Not to mention all the other amazing rewards that working at AT&amp;T offers. Individual starting salary within this range may depend on geography, experience, expertise, and education/training.
Joining our team comes with amazing perks and benefits:<ul><li>
Medical/Dental/Vision coverage</li><li>
401(k) plan</li><li>
Tuition reimbursement program</li><li>
Paid Time Off and Holidays (based on date of hire, at least 23 days of vacation each year and 9 company-designated holidays)</li><li>
Paid Parental Leave</li><li>
Paid Caregiver Leave</li><li>
Additional sick leave beyond what state and local law require may be available but is unprotected</li><li>
Adoption Reimbursement</li><li>
Disability Benefits (short term and long term)</li><li>
Life and Accidental Death Insurance</li><li>
Supplemental benefit programs: critical illness/accident hospital indemnity/group legal</li><li>
Employee Assistance Programs (EAP)</li><li>
Extensive employee wellness programs</li><li>
Employee discounts up to 50% off on eligible AT&amp;T mobility plans and accessories, AT&amp;T internet (and fiber where available) and AT&amp;T phone</li></ul></div></div>
Weekly Hours:
40
Time Type:
Regular
Location:
Chantilly, Virginia
It is the policy of AT&amp;T to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, AT&amp;T will provide reasonable accommodations for qualified individuals with disabilities. AT&amp;T is a fair chance employer and does not initiate a background check until an offer is made.</div>

Quality Assurance Specialist (Government)

Bio-Techne

<div>By joining Bio-Techne, you&rsquo;ll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.
Pay Range:
$55,600.00 - $91,450.00
Position Summary:
Are you passionate about science and have experience in quality assurance related activities? This could be the opportunity for you! To join a company that develops and provides a unique and cutting edge lineup of products and tools used by life science researchers, pharma, and diagnostic companies to make scientific discoveries, medical breakthroughs, understand the cause of diseases, develop new treatments, and much more!
As a Quality Assurance (QA) Specialist you will support the quality functions of Bio-Techne through quality systems development and improvement, document and records review, auditing, and other quality functions. The QA Specialist will understand and follow appropriate quality procedures to meet compliance standards, including ISO 9001, ISO 13485, and 21CFR820.
Key Responsibilities:
<ul><li>Participate in cross-functional team meetings as a quality representative, assist in management of quality issues and offer input representing quality assurance (new product design, data reviews or root cause investigations).
</li><li>Work collaboratively with all functions to ensure understanding and conformance with quality requirements.
</li><li>Assist in Quality review of newly written or revised GMP specifications, documents, labels and literature for accuracy and completeness. Write documents as needed.
</li><li>Assist in Quality review of batch records for product manufacturing.
</li><li>Assist in monitoring quality systems through monthly complaint meetings, monthly reports, trending, and annual quality review.
</li><li>Assist in writing or reviewing newly written or revised validation plans and review the completed validations for accuracy and completeness.
</li><li>Assist in maintaining and/or developing companywide Quality systems including, but not limited to, quality audits, product validation, document control, acceptance activities, production and process control, and corrective and preventive action.
</li><li>Follows company policies and practices as outlined in the Handbook and follows guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance with the job.
</li><li>Follows applicable standard operating procedures (SOPs), including a good understanding of quality associated SOPs.
</li><li>Propose process improvements and areas for improvement to supervisor.
</li><li>Conduct inspections of raw materials, intermediates, and finished goods to ensure specifications and quality standards are met.
</li><li>Conduct inspection of product literature and labels to ensure accuracy.
</li><li>Performs additional duties as assigned.
</li></ul>Job Qualifications
Education and Experience:
<ul><li>This position requires a minimum of a bachelor&rsquo;s degree in a biological or chemical scientific discipline, with 1 - 3 years of related experience in quality activities in a science related field, or equivalent combination of education and experience.
</li><li>Must have the ability to work in a fast-paced environment with an attention to detail, organization, and time management skills. Should be able to work individually, but also as a contributing member of internal and cross-functional teams maintaining good communication skills, both verbally and in writing.
</li><li>Experience and understanding of ISO 9001 or ISO 13485 is preferred.
</li></ul>Knowledge, Skills, and Abilities:
<ul><li>Attention to detail and organizational skills are required
</li><li>Working knowledge of Microsoft Word and Excel are required
</li><li>Computer entry, typing, or electronic document filing skills are require
</li><li>Must be able to work in a fast-paced environment where multitasking is required
</li><li>Must have excellent verbal and written communication skills
</li><li>Knowledge of technical, regulatory, quality and production management systems
</li><li>Knowledge of documentation principles and processes
</li><li>Skills in accuracy, clarity, and proofreading
</li><li>Skills in problem solving, root cause analysis, and appropriately evaluate a course of actions
</li></ul><div><div><div><div>Why Join Bio-Techne:
<ul><li><h3 class="jobSectionHeader">We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.
</h3></li><li><h3 class="jobSectionHeader">We invest in our employees&rsquo; financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.
</h3></li><li><h3 class="jobSectionHeader">We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.
</h3></li><li><h3 class="jobSectionHeader">We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.
</h3></li><li><h3 class="jobSectionHeader">We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.
</h3></li><li><h3 class="jobSectionHeader">We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.
</h3></li></ul>Bio-Techne is an E-Verify Employer in the United States.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.</div></div></div></div></div>

Advanced Quality Assurance Specialist

Planet Pharma

<div>
 
 Responsibilities
 
 
 
 This role is responsible for executing Quality function deliverables to support Contract Manufacturing Organizations (CMOs) involved in the production of drug substance in support of rapidly growing Clinical and Commercial Programs. This hybrid role is expected to support Monday &ndash; Friday during the hours of 8am to 4pm. Expected to be on-site in Cambridge, MA location, three (3) days per week with Thurs being a required on-site day. The remining 2 on-site days can be discretionary.
 
 
 This position will manage QA tasks such as deviations, change controls, and investigations involved in production of drug substance. In this role, the person will be responsible for internal QA review and approval of documentation required to support batch manufacturing and disposition. The QA Specialist role ensures that establishes standards and practices and maintains documented procedures and instructions to satisfy cGMPs and Good Documentation Practices for all clinical and commercial drug disposition activities. This individual will work closely with Quality Assurance, External Manufacturing, Quality Control, Process Sciences and Regulatory teams.
 
 
 
 Summary Of Key Responsibilities
 
 
 
 <ul>
 <li>
 Ensure product quality at drug substance contract manufacturing operations, while developing and maintaining relationships.
 </li>
 <li>
 Perform functions and make decisions consistent with cGMPs, GDPs and quality governance
 </li>
 <li>
 Provide QA support for the transfer of manufacturing processes and analytical methods for products to CMOs
 </li>
 <li>
 Independent review and approval of change controls, deviations, OOS, CAPA, and metrics.
 </li>
 <li>
 Gather and provide metric information
 </li>
 <li>
 Perform Batch Disposition in accordance with all applicable SOPs
 </li>
 <li>
 Review and approval of Master Batch Records and executed Batch Records.
 </li>
 <li>
 Support SOP generation and revisions
 </li>
 <li>
 Review of Protocols, Reports, Stability data and associated reports as needed
 </li>
 <li>
 Support of Process performance qualification (PPQ) activities, including review of relevant validation protocols and reports
 </li>
 <li>
 Support and preparation for company and Agency Inspections conducted at our CMOs, as needed.
 </li>
 <li>
 Maintain 100% training compliance
 </li>
 <li>
 Additional duties as assigned.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 A minimum of Bachelor&rsquo;s degree in sciences or engineering
 </li>
 <li>
 A minimum of 3 years of QA operations experience in a GMP manufacturing facility
 </li>
 <li>
 Excellent understanding of FDA, EMA regulations and ICH guidelines
 </li>
 <li>
 Excellent organizational, communication, and interpersonal skills
 </li>
 <li>
 Experience with electronic Quality Management Systems (experience with Veeva is a plus)
 </li>
 <li>
 Experience with electronic enterprise resource planning systems (experience in SAP is a plus)
 
 
 </li>
 </ul>
 Pay ranges between 55-63/hr based on experience
</div>

Kwanso

As a Software Quality Assurance Engineer, you will be responsible for designing, implementing, and executing comprehensive test plans tailored to each project or service offering. Collaborating closely with cross-functional teams, including developers, project managers, and clients, you will help ensure that our solutions meet or exceed client expectations and industry standards, including modern AI-powered and LLM-based applications.If you envision yourself working with smart engineers on &amp; across the teams to deliver top-notch projects &amp; be the best-in-class professional, Kwanso is where you need to be!WHAT YOU&rsquo;LL DO:<ul><li>Validate AI-driven features, including LLM-based functionalities (e.g., chatbots, recommendation systems, content generation).</li><li>Design and execute test strategies for AI systems, including prompt testing, response validation, and edge-case handling.</li><li>Evaluate LLM outputs for accuracy, relevance, hallucinations, bias, and safety compliance.</li><li>Perform prompt engineering for testing purposes to simulate diverse real-world user inputs and scenarios.</li><li>Develop and maintain test datasets for validating AI models and LLM outputs.</li><li>Collaborate with engineering teams to define evaluation metrics for AI systems (e.g., precision, recall, latency, response quality).</li><li>Conduct regression testing for AI models, ensuring model updates do not degrade performance.</li><li>Test API integrations with AI services (e.g., OpenAI, Claude, etc.).</li><li>Ensure compliance with AI safety, ethical standards, and data privacy requirements.</li><li>Automate testing workflows for AI/LLM systems using relevant frameworks and tools.</li><li>Monitor and report real-world performance issues in AI systems post-deployment.</li></ul>WHAT YOU&rsquo;LL BRING:Bachelor&rsquo;s degree in computer science, information technology, or a similar fieldMinimum 2 years experience working as a Software Quality Assurance EngineerStrong understanding of software testing principles and methodologies, including experience with manual and automated testing techniques.Basic understanding of AI/ML concepts and Large Language Models (LLMs).Experience or exposure to testing AI-driven or data-driven applications.Ability to create detailed, comprehensive test plans and test cases based on project requirements and specifications.Excellent analytical and problem-solving skills, with a keen eye for detail.HOW WE WORK:Annual Pay Raise - Higher the performance, better the numbersProvident Fund &amp; EOBI - Adds up to your retirement plansHealth Insurance - We&rsquo;ve got you coveredAnnual Leaves - Take your leaves or take the cash insteadWork Hours Relaxation - 20 Paid days off in a year other than the gazetted holidaysInterest Free Loan facility - Avoid hefty banking interestsWHO WE ARE:We are an established custom design &amp; development company with a proven record of delivering tons of successful projects to our partners including startups, small &amp; mid-sized companies &amp; brands with no specific industry vertical.Kwanso was founded in April, 2014 in Lahore &amp; later formed its subsidiary in Bay Area (SF) in 2015.Our work comprises modern tech that enables us to be the experts in the modern open-source technology stacks for web &amp; mobile. We want to stay highly focused on cool tech.We have delivered for brands like Whirlpool, Sears, UFC, Kimberly Clark, PBS Kids &amp; Bushnell to name a few, our complete client base is from the United States.DISCLAIMER:Kwanso is an equal opportunity employer: we value diversity &amp; do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age or marital status etc.By submitting your application, you agree that Kwanso may collect your personal data for recruiting &amp; related purposes.Work Location: In person

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Quality Assurance Specialist

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Quality Assurance Specialist - 60026087

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Quality Assurance Specialist

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