qa specialist

giftHEALTH

<div><h3 class="jobSectionHeader"><b>Position Summary</b></h3><p>
We are seeking a <b>QA Specialist &ndash; Process Automation</b> to join our Gifthealth team. This is an entry-level role on the QA team within <b>Operations / Process Automation</b>, built for a detail-oriented pharmacy technician who is eager to grow into the intersection of pharmacy operations and health technology. Working under the close direction of the QA Lead, the QA Specialist performs structured day-to-day quality checks across BestRx and Gifthealth&rsquo;s automation workflows, documents findings clearly and consistently, and flags issues for triage and escalation.</p><p>
No prior QA or automation experience is required. Full training on systems, workflows, and documentation standards will be provided. What matters most is genuine attention to detail and the curiosity to ask why something does not look right.</p><h3 class="jobSectionHeader"><b>
Key Responsibilities</b></h3><ul><li>
Perform structured daily quality checks within BestRx and connected software automation systems, reviewing for issues such as duplicate prescriptions, intake mismatches, and workflow errors.</li><li>
Document issues clearly and consistently using standardized templates, capturing what the problem is, where it occurred, and what evidence supports the finding.</li><li>
Escalate findings to the QA Lead with clear, organized documentation so the appropriate teams can act quickly.</li><li>
Participate in testing of system fixes and workflow updates deployed by engineering, confirming that changes work as expected.</li><li>
Maintain organized issue logs and follow up on open items to ensure nothing falls through the cracks.</li><li>
Support the QA Lead in building training materials and QA best practice guides as the team grows.</li><li>
Handle all work in compliance with HIPAA requirements and internal pharmacy privacy standards.</li></ul><h3 class="jobSectionHeader"><b>
Qualifications</b></h3><ul><li><b>
Education: </b>High school diploma or equivalent required.</li><li><b>
Experience: </b>0&ndash;2 years; new graduates and RPT trainees welcome. Prior QA or automation experience not required. Any pharmacy operations background is helpful context.</li><li><b>
Licensure/Certification: </b>Active Registered Pharmacy Technician (RPT) credential required. Certified Pharmacy Technician (CPhT) credential strongly preferred and will be prioritized in screening.</li><li><b>
Skills (Required): </b>Strong attention to detail; ability to stay organized across multiple open items simultaneously; clear written communication skills; willingness to learn new systems, processes, and tools; adherence to HIPAA requirements and pharmacy privacy standards.</li><li><b>
Skills (Preferred): </b>BestRx experience or familiarity with any pharmacy management system; experience in a retail, specialty, or mail-order pharmacy environment; basic troubleshooting instincts including a habit of documenting what was tried before escalating.</li></ul><h3 class="jobSectionHeader"><b>
Desired Attributes</b></h3><ul><li>
Meticulous by nature &mdash; catches what others miss and documents findings completely without needing to be reminded.</li><li>
Curious when something looks wrong &mdash; investigates before escalating and documents what was tried.</li><li>
Communicates clearly in writing &mdash; can describe an issue so that someone else understands exactly what happened, where, and why it matters, without follow-up questions.</li><li>
Sees this role as an on-ramp into a more technical career &mdash; eager to grow and proactive about asking questions when something is unclear.</li><li>
Comfortable with evolving processes &mdash; frames change as an opportunity to contribute rather than a source of frustration.</li></ul><h3 class="jobSectionHeader"><b>
Work Environment</b></h3><ul><li><b>
Location: </b>Columbus, OH (Hybrid or Remote).</li><li><b>
Schedule: </b>Full-time, salaried.</li><li>
Work is performed primarily using computer-based systems. Regular collaboration with the QA Lead and interaction with engineering and pharmacy operations teams as needed.</li></ul><h3 class="jobSectionHeader"><b>
Key Essential Functions</b></h3><ul><li>
Must be able to remain in a stationary position for extended periods while performing computer-based quality checks and documentation tasks.</li><li>
Must be able to work on a computer for the majority of the workday, including use of pharmacy management systems, issue-tracking tools, and documentation platforms.</li><li>
Must be able to communicate clearly in writing to document findings and escalate issues accurately.</li><li>
Must be able to work scheduled shifts reliably and maintain focus and attention to detail throughout the workday.</li><li>
Must be able to handle protected health information in compliance with HIPAA and internal privacy policies.</li></ul><h3 class="jobSectionHeader"><b>
Employment Classification</b></h3><p><b>
Status:</b> Full-time<br>
<b>FLSA:</b> Non-Exempt</p><h3 class="jobSectionHeader"><b>
Equal Employment Opportunity (EEO) Statement</b></h3><p>
Gifthealth is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions are made without regard to race, color, religion, sex, sexual orientation, gender identity, transgender status, national origin, age, disability, veteran status, or any other legally protected status. We celebrate diversity and are committed to creating an inclusive environment for all employees.</p><h2 class="jobSectionHeader"><b>
Disclaimer</b></h2><p>
This job description is intended to describe the general nature and level of work being performed. It is not intended to be an exhaustive list of all responsibilities, duties, or skills required of personnel. Gifthealth reserves the right to modify job duties or descriptions at any time.</p></div>

QA Specialist – Process Automation

Baylor Scott & White Health

<div><h4 class="jobSectionHeader"><b>About Us</b></h4><p>
Here at Baylor Scott &amp; White Health we promote the well-being of all individuals, families, and communities. Baylor Scott and White is the largest not-for-profit healthcare system in Texas that empowers you to live well.</p><p>
Our Core Values are:</p><ul><li>
We serve faithfully by doing what's right with a joyful heart.</li><li>
We never settle by constantly striving for better.</li><li>
We are in it together by supporting one another and those we serve.</li><li>
We make an impact by taking initiative and delivering exceptional experience.</li></ul><h4 class="jobSectionHeader"><b>
Benefits</b></h4><p>
Our benefits are designed to help you live well no matter where you are on your journey. For full details on coverage and eligibility, visit the Baylor Scott &amp; White Benefits Hub to explore our offerings, which may include:</p><ul><li>
Immediate eligibility for health and welfare benefits</li><li>
401(k) savings plan with dollar-for-dollar match up to 5%</li><li>
Tuition Reimbursement</li><li>
PTO accrual beginning Day 1</li></ul><p><i>
Note: Benefits may vary based upon position type and/or level.</i></p><h4 class="jobSectionHeader"><b>
Job Summary</b></h4><p>
The Lab QA Specialist 2 develops, coordinates, monitors, and maintains department policies on inspection readiness, employee safety, and quality assurance. This includes employee education and training on department responsibilities and safety. Maintains knowledge of a broad range of external regulatory standards related to laboratory operations.</p><h4 class="jobSectionHeader"><b>
Essential Functions of the Role</b></h4><ul><li>
Coordinates the laboratory safety team and consults with the laboratory and institutional safety director on all safety policies and procedures.</li><li>
Ensures that safety standards and regulations are followed by laboratory staff.</li><li>
Establishes and maintains regulatory compliance and safety policies as required by external regulatory agencies (e.g. OSHA, TJC, CAP, CLIA, etc.).</li><li>
Develops, coordinates, conducts, and maintains documentation of employee continuing education, safety education, and training.</li><li>
Maintains records for CME and employee ability, as required and in coordination with management, supervisors, and human resources.</li><li>
Oversees department quality plans and all associated local quality initiatives. Performs all delegated functions as defined by facility CLIA Director.</li><li>
Monitors laboratories to ensure regulatory compliance and reports findings to appropriate institutional and departmental administrative team.</li><li>
Instructs MT and MLT students, Pathology Residents, and Medical Students in safety and regulatory issues.</li><li>
Represents the department as a functioning member of institutional safety and quality improvement committees.</li></ul><h4 class="jobSectionHeader"><b>
Key Success Factors</b></h4><ul><li>
Knowledge of laboratory regulations, protocols and procedures.</li><li>
Data and critical thinking abilities.</li><li>
Ability to comprehend and communicate instructions.</li><li>
Ability to perform laboratory protocols and procedures.</li><li>
Skill in the use of computers and related software applications.</li><li>
Knowledge of safety and infection control standards.</li><li>
Ability to work in a team environment.</li><li>
Provides training and opportunities for continuing education.</li><li>
Effective leadership and social skills.</li></ul><h4 class="jobSectionHeader"><b>
Belonging Statement</b></h4><p>
We believe that all people should feel welcomed, valued and supported.</p><p><b>
QUALIFICATIONS</b></p><ul><li>
 EDUCATION - Bachelor's or 4 years of work experience above the minimum qualification</li><li>
 EXPERIENCE - 4 Years of Experience</li><li>
 CERTIFICATION/LICENSE/REGISTRATION -</li></ul><p>
ASCP-BloodBanking Technologist (ASCP-BB), ASCP-Chemistry Technologist (ASCP-C), ASCP-Cytogenetics Technologist (ASCP-CG), ASCP-Cytologist (ASCP-CT), ASCP-Hematology Technologist (ASCP-H), ASCP-Histotechnician (ASCP-HT), ASCP-Histotechnologist (ASCP-HTL), ASCP-Microbiology Technologist (ASCP-M), Molecular Biology Technologist (ASCP-MB), ASCP-Blood Banking Specialist (ASCP-SBB), ASCP-Chemistry Specialist (ASCP-SC): Must have one of the following:<br>
ASCP-BB<br>
ASCP C<br>
ASCP-CG<br>
ASCP-CT<br>
ASCP-H<br>
ASCP-HT<br>
ASCP-HTL<br>
ASCP-M<br>
ASCP-MB<br>
ASCP-SBB<br>
ASCP-SC<br>
ASCP-SH<br>
ASCP-SM<br>
CHS-ABHI<br>
CHT-ABHI<br>
CLS<br>
MLS<br>
MT<br>
SCT<br>
SCYM<br>
SMB.<br>
<br>
ASCP-Hematology Specialist (ASCP-SH), ASCP-Microbiology Specialist (ASCP-SM), Cert Histocompatibility Spec (CHS-ABHI), Cert Histocompatibility Techno (CHT-ABHI), Clinical Laboratory Scientist (CLS), Medical Laboratory Scientist (MLS), Medical Technologist (MT), Specialist in Cytology-ASCP (SCT), Specialist in Cytometry-ASCP (SCYM), Molecular Biology Spec-ASCP (SMB).</p></div>

Lab QA Specialist 2

SYSTRA

<div>:
<div>
SYSTRA is one of the world's leading engineering and consultancy groups specialising in public transport and sustainable mobility. With over 10,300 employees, SYSTRA's mission is to design safe and sustainable transport solutions to bring people together, develop social inclusion and facilitate access to employment, education and leisure throughout the world.</div><div>
For 65 years, the Group has been working alongside cities and regions to contribute to their development by creating, improving and modernising their infrastructure and transport systems, throughout the life cycle of their projects. SYSTRA is involved from the earliest stages of design through to the testing, deployment and maintenance phases. The company provides all its services in over 80 countries worldwide and generates 74% of its turnover internationally. With its new services, SYSTRA supports its clients and partners in their digital, ecological and energy transition, in order to invent the mobility of tomorrow.</div>
Context:
<p>
The QA/QC Specialist will provide quality assurance (QA) and quality control (QC) support activities on assigned functional areas of the Rail/Metro project to ensure that they are in accordance with the client&rsquo;s and contractual specifications.</p><div>
The QA/QC Specialist will report to the QA/QC Manager and will also regularly interact with representatives from a variety of functional groups, including program management, engineering and construction</div>
Missions/Main Duties:
<ul><li>To STOP the work, in the event of identifying any activity where serious breach of Health, Safety or Environmental standard is witnessed.</li><li>
To conduct audits to verify that plans &amp; procedures are being followed, and documentary evidence is produced and maintained (Desirable, non-essential)</li><li>
To coordinate with the construction staff. Plan in advance any necessary inspections and testing activities.</li><li>
In respect to the adherence to the Contractors Project Quality Assurance and Quality Control Plans &amp; Procedures by the Contractors their Sub &ndash; Contractors and their Suppliers in the first instance by closely monitoring the works.</li><li>
Maintain surveillance of DB Contractors QC Inspectors, collaborate with Inspectors.</li><li>
Site visits for visual verification of procedure adherence, feedback from NCR&rsquo;s and feedback from progress meetings and individual reporting of concerns from general workforce, Supervisors and Management.</li><li>
Ensure As-Built Quality Records are produced in respect to the ITPs.
</li><li>Surveillance of ITP content and the required compilation of records referenced within in respect to materials specifications, tolerances, standards, there certification to compliance, their traceability and their use in the realisation of the product.</li><li>
Temperatures where applicable, the timely taking of samples, their handling, curing, storage and testing.</li><li>
The existence of authorised for use ITPs at the workplace, before\during the start of works activities.
</li><li>Ensure site QA/QC compliance through on site surveillance or via QC Inspector reporting. Visual, Feedback and written reporting.</li><li>
To plan daily inspection activities and surveillances.</li></ul>
Profile/Skills:
<ul><li>Bachelor&rsquo;s degree in civil engineering with experience gained within heavy infrastructure, civil engineering, or rail &amp; metro projects.</li><li>
Knowledge of QA\QC principles tools &amp; techniques, ideally a quality qualification, or membership of a professional quality body.</li><li>
A minimum of 8 years&rsquo; experience in quality assurance and quality control on either infrastructure, civil engineering or rail projects</li><li>
Excellent English language, verbal, reading and writing skills
</li></ul>:
<div>
Systra is an equal opportunities company; this position is open to all applicants.</div></div>

QA/QC Specialist

Specart Technologies PVT LTD

<div>
 <p>
  <strong>
   Location:
  </strong>
  Lahore, Punjab, Pakistan (On-site)
 </p>
 <p>
  <strong>
   Job Type:
  </strong>
  Full-time | Night Shift
 </p>
 <p>
  <strong>
   Industry:
  </strong>
  Media Production, Animation, Motion Pictures &amp; Film
 </p>
 <p>
  <strong>
   Experience Level:
  </strong>
  Associate / Mid-Senior level
 </p>
 <strong>
  About the Role
 </strong>
 <p>
  <strong>
   SPECART
  </strong>
  is actively looking for a highly meticulous
  <strong>
   Video Quality Assurance Specialist
  </strong>
  (Video QA / QC Specialist) to join our fast-growing post-production studio in Lahore.
 </p>
 <p>
  As our Video QA Specialist, you will be the final line of defense, conducting frame-by-frame inspections on high-end video editing projects, 2D/3D animations, and motion graphics to ensure they meet elite international delivery standards.
 </p>
 <strong>
  Key Responsibilities (What You'll Do)
 </strong>
 <ul>
  <li>
   <strong>
    Quality Control &amp; QA Testing:
   </strong>
   Review exported timelines, videos, and multi-cam sequences frame-by-frame to isolate and log rendering artifacts, visual glitches, and dropped frames.
  </li>
  <li>
   <strong>
    Technical Compliance Checking:
   </strong>
   Audit final video renders for correct technical specifications, including aspect ratios, video codecs, bitrates, frame rates, resolutions, and file formatting.
  </li>
  <li>
   <strong>
    Animation &amp; Motion Graphics Audit:
   </strong>
   Meticulously review visual effects (VFX), typography positioning, keyframe pacing, lower-thirds, and sub-titling accuracy.
  </li>
  <li>
   <strong>
    Audio-to-Video Syncing:
   </strong>
   Perform rigorous audio quality checks to ensure flawless synchronization between video tracks, background scores, sound effects, and voiceovers.
  </li>
  <li>
   <strong>
    Cross-functional Collaboration:
   </strong>
   Document workflow defects clearly and collaborate during the night shift with our creative Video Editors, Animators, and Motion Graphic Designers for rapid revision iterations.
  </li>
 </ul>
</div>


Video Quality Control Specialist

Wellbox Health

<div>
 <strong>
  Position Summary
  <br/>
  <br/>
 </strong>
 The QA Specialist is responsible for reviewing, analyzing, and improving the accuracy, completeness, and quality of documentation, workflows, and operational outputs across the department. This role ensures that work meets organizational standards, supports compliance, identifies process improvement opportunities, and provides feedback to team members to enhance performance. The QA Specialist collaborates closely with clinical, operational, and administrative teams to promote consistency, reliability, and quality across all processes.
 <br/>
 <br/>
 <strong>
  Essential Functions
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Conduct quality reviews of documentation, records, and workflows to ensure accuracy, completeness, and adherence to organizational standards.
  </li>
  <li>
   Provide constructive, timely feedback to staff to improve documentation quality and compliance.
  </li>
  <li>
   Track and report quality trends, common errors, and opportunities for training or workflow improvement.
  </li>
  <li>
   Collaborate with team leads and managers to refine documentation standards, processes, and QA methodologies.
  </li>
  <li>
   Ensure compliance with HIPAA and other regulatory or company-specific guidelines.
  </li>
  <li>
   Assist in identifying missing or incomplete information in systems and communicate findings to the appropriate departments.
  </li>
  <li>
   Support internal and external audit requests by gathering and verifying necessary documentation.
  </li>
  <li>
   Maintain detailed and organized QA logs, reports, and documentation of findings.
  </li>
  <li>
   Participate in training initiatives, coaching sessions, and quality-focused meetings.
  </li>
  <li>
   Serve as a resource for team members regarding documentation standards, processes, and quality expectations.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Required Education And Experience
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Certification or training in a healthcare or documentation-related field (e.g., CMA, medical terminology coursework, HIM coursework), or equivalent professional experience.
  </li>
  <li>
   Experience working with documentation-heavy workflows, preferably within healthcare or a regulated environment.
  </li>
  <li>
   Strong written communication skills and excellent attention to detail.
  </li>
  <li>
   Proficiency with the Windows platform, Microsoft Office Suite, and computer-based tools.
  </li>
  <li>
   Experience working in electronic systems or EHRs (if healthcare-specific).
  </li>
  <li>
   Strong analytical skills, including the ability to identify error patterns and recommend improvements.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Competencies And Preferred Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Background in quality assurance, auditing, or compliance.
  </li>
  <li>
   Experience in Chronic Care Management or clinical documentation review.
  </li>
  <li>
   Advanced Excel skills (pivot tables, VLOOKUP/XLOOKUP, advanced formulas).
  </li>
  <li>
   Prior experience providing training or feedback to staff.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Position Type And Expected Hours Of Work
  <br/>
  <br/>
 </strong>
 This is a regular, full-time position that operates in an office or remote work environment.
 <br/>
 <br/>
 <strong>
  Physical Requirements
  <br/>
  <br/>
 </strong>
 This is a sedentary position that requires the ability to sit or stand for extended periods and work at a computer.
 <br/>
 <br/>
 <strong>
  Work Environment
  <br/>
  <br/>
 </strong>
 This is a remote position. We will provide you with the equipment and software needed, such as a laptop and necessary accessories. Since we&rsquo;re dedicated to offering our clients the best experience possible, a high-speed internet connection and a private space free from outside noise and distraction, including noise and distractions from pets or children, and that complies with HIPAA privacy laws, is required.
</div>


Quality Assurance Specialist

Kelly Science, Engineering, Technology & Telecom

<div>
 <p>
  Kelly&reg; Science &amp; Clinical is seeking a Senior Quality Assurance (QA) Specialist for
  <strong>
   a 6-month contract
  </strong>
  position at
  <strong>
   a premier biotech company
  </strong>
  in
  <strong>
   San Jose, CA
  </strong>
  . If you&rsquo;re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Pay Rate:
  </strong>
 </p>
 <p>
  $50-55/hour
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Overview:
  </strong>
 </p>
 <p>
  In this role, you will ensure quality and compliance by managing documentation, supporting manufacturing operations, overseeing product release activities, handling investigations and quality records, and assisting with audits as a key member of the QA team.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Schedule:
  </strong>
 </p>
 <p>
  Monday-Friday, 8:00am to 5:00pm, occasional weekend/evening shifts on a rotation basis (every 4-5 weeks)
 </p>
 <p>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Responsibilities:
  </strong>
 </p>
 <ul>
  <li>
   Author, review, and revise documentation such as SOPs, policies, and standards to ensure strict adherence to GMP (Good Manufacturing Practice) requirements.
  </li>
  <li>
   Provide direct, on-floor QA support for manufacturing operations.
  </li>
  <li>
   Perform and oversee lot disposition and product release activities for clinical and commercial products, ensuring compliance with regulatory and quality standards.
  </li>
  <li>
   Conduct thorough reviews of batch production records, quality control testing data, and equipment maintenance/calibration documentation, and lead investigations related to product quality.
  </li>
  <li>
   Collaborate with the QA team to maintain accurate quality records and assist in hosting client and regulatory audits, supporting a culture of continuous improvement and compliance.
  </li>
  <li>
   Other duties as assigned.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications:
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Science or related field.
  </li>
  <li>
   5+ years of QA experience in a biotech or pharma GMP environment.
  </li>
  <li>
   Experience with lot release and disposition.
  </li>
 </ul>
</div>


Senior Quality Assurance Specialist

Arcadia Strategy Group

<div><div><p>Arcadia is seeking a Senior Software Quality Assurance Specialist/Application Tester to support multiple software applications in various stages of deployment, from emerging technologies to legacy systems.</p>
</div><div><h3 class="jobSectionHeader"><b>About Arcadia Strategy Group LLC</b></h3>
<div><div>Arcadia Strategy Group supports federal government partners and select private sector clients with solutions that improve program efficiencies and enhance national security.
</div></div></div><div><h3 class="jobSectionHeader"><b>Description</b></h3>
<div><div><p><b>Description:</b> The tester will work as part of a small test team and support automated and manual testing efforts. The role requires modern automated testing knowledge and the ability to perform manual testing when automation is impractical. The tester may also support performance and load testing with application developers. This position requires an active TS/SCI with Polygraph on day one.</p><p><b>
Requirements:</b></p><ul><li>Experience with SQL queries for data validation, including Oracle, Postgres, or MySQL.</li><li>Expertise with Selenium WebDriver.</li><li>Strong experience writing automated test code in Java.</li><li>Ability to evaluate developer assignments, understand requirements independently, and engineer tests for successful and failure conditions.</li><li>Experience using an IDE such as IntelliJ, Eclipse, or NetBeans.</li><li>Experience working in a Linux environment, including Bash scripting or vi.</li><li>Expertise writing test plans, cases, procedures, scripts, and scenarios.</li><li>Demonstrated experience with manual and automated testing processes.</li><li>Ability to work well in a constantly evolving environment.</li><li>Ability to ensure QA and testing approaches account for known vulnerabilities and best practices.</li><li>Experience conducting and reporting testing using repeatable industry best-practice processes.</li><li>Ability to maintain and update the test environment.</li><li>Development skills appropriate for automated testing.</li><li>Hands-on experience with testing tools such as JMeter and/or Selenium.</li></ul><p><b>
Benefits:</b> At ASG, we recognize and reward your contributions. Our benefits for full-time employees include employer-sponsored health insurance, matching 401k retirement plan, and paid leave.</p></div></div></div></div>

Senior Test Automation Engineer (TS/SCI + polygraph)

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