manager qa

ProKidney Corp.

<div>
 <strong>
  Position Summary:
  <br/>
  <br/>
 </strong>
 The Quality Assurance On-The-Floor (OTF) Manager is responsible for leading the QA On-The-Floor team and providing real-time quality oversight of clinical and commercial manufacturing activities at ProKidney&rsquo;s cGMP site. Reporting to the VP of Quality, this role managers daily floor support operations, ensures compliance with GMP and regulatory requirements, and partners closely with Manufacturing, Quality Control, Supply Chain, and Facilities to maintain a state of control on the production floor.
 <br/>
 <br/>
 This position is located fully onsite in Winston Salem, NC.
 <br/>
 <br/>
 <strong>
  Team Leadership &amp; Oversight
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Manage, develop, and coach the QA On-the-Floor team; ensure training, qualification, and performance expectations are met.
  </li>
  <li>
   Assign and approve work performed by direct reports, including documentation reviews and floor support activities.
  </li>
  <li>
   Maintain team readiness by ensuring all OTF personnel remain gown-qualified and trained on current procedures.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Manufacturing Floor Support &amp; Quality Oversight
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Oversee and publish daily/weekly QA floor support schedules aligned with the manufacturing schedule.
  </li>
  <li>
   Provide real-time QA presence on the manufacturing floor, including routine walkthroughs, observation of operations, support during processing, and reinforcement of cleanroom behaviors.
  </li>
  <li>
   Identify, document, and escalate GMP issues or atypical events during manufacturing.
  </li>
  <li>
   Perform and/or oversee real-time batch record review to ensure accuracy and completeness.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Quality Decision Making &amp; Issue Resolution
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Make routine QA decisions related to room/equipment release, line clearance, and documentation accuracy.
  </li>
  <li>
   Support and/or approve alarms, return-to-service documentation, deviations, change controls, and other quality records related to floor operations.
  </li>
  <li>
   Partner with Manufacturing to troubleshoot operational issues and implement corrective actions.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Documentation &amp; Compliance Activities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Ensure timely review of GMP documents (forms, logbooks, testing documentation, alarms, kitting, etc.).
  </li>
  <li>
   Ensure quarantined materials are stored and managed appropriately post-manufacturing.
  </li>
  <li>
   Author, revise, and review SOPs and quality procedures related to on-the-floor operations.
  </li>
  <li>
   Support internal audits, regulatory inspections, and compliance initiatives.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Cross Functional Collaboration
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Collaborate in a fast-paced, matrixed environment to ensure alignment on quality expectations and operational priorities.
  </li>
  <li>
   Participate in cross-functional quality teams and process improvement initiatives.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Other Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Maintain standards for accurate documentation, data integrity, and compliance in all QA-OTF activities.
  </li>
  <li>
   Perform other duties as assigned.
  </li>
  <li>
   <strong>
    Education And Experience:
   </strong>
  </li>
  <li>
   Bachelor&rsquo;s degree in applied science or related field.
  </li>
  <li>
   5+ years relevant QA experience in cGMP aseptic manufacturing, preferred as Quality on the floor
  </li>
  <li>
   Proven, hands-on knowledge of commercial GMP regulations for sterile manufacturing
  </li>
  <li>
   Strong organizational, analytical, and time management skills.
  </li>
  <li>
   Ability to work well in a team environment with positive attitude.
  </li>
  <li>
   Excellent communication skills with strong attention to detail.
  </li>
  <li>
   Ability to handle multiple tasks simultaneously.
  </li>
  <li>
   Demonstrated working knowledge of FDA, EU, and ICH regulatory requirements.
  </li>
  <li>
   Physical ability to perform frequent tasks requiring strength and mobility.
   <br/>
   <br/>
  </li>
 </ul>
 ProKidney is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law.
 <br/>
 <br/>
 Applicants must be eligible to work in the United States without the need for work visa or residency sponsorship.
</div>


Manager, QA Floor Support

Mobilink Bank

<div>
 <p>
  <strong>
   Job Title:
  </strong>
  Assistant Manager, QA Automation
 </p>
 <p>
  <strong>
   Grade:
  </strong>
  OG-I
 </p>
 <p>
  <strong>
   Reports to:
  </strong>
  Executive Manager, IT Governance
 </p>
 <p>
  <strong>
   Location:
  </strong>
  Islamabad
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   About the Role:
  </strong>
 </p>
 <p>
  As an Assistant Manager &ndash; QA Automation, you will be responsible for designing, developing, and executing test plans to ensure high-quality deliverables. You will collaborate closely with developers, product managers, and other stakeholders to uphold the highest standards of quality across our products. This position is ideal for someone who is detail-oriented and passionate about quality.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Job Description:
  </strong>
 </p>
 <ul>
  <li>
   Design, implement, and maintain comprehensive test plans, test cases, and test scripts Identify, log, and track defects with precision, ensuring timely resolution through collaboration with development teams
  </li>
  <li>
   Partner with product managers and developers to clarify requirements and define acceptance criteria
  </li>
  <li>
   Conduct performance, load, and stress testing to ensure system scalability and reliability
  </li>
  <li>
   Develop and maintain automated test frameworks and scripts for regression and performance testing
  </li>
  <li>
   Ensure timely execution of tests and clear reporting of results
  </li>
  <li>
   Advocate for quality best practices across the engineering organization, influencing processes, tools, and culture
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Requirements:
  </strong>
 </p>
 <ul>
  <li>
   Bachelor's in Computer Science, Software Engineering, or a related field
  </li>
  <li>
   3&ndash;5 years of professional experience in Quality Assurance and Test Automation
  </li>
  <li>
   Good understanding of test automation tools and frameworks
  </li>
  <li>
   Experience with API testing tools (e.g., Postman, REST Assured)
  </li>
  <li>
   Solid understanding of STLC and QA methodologies Familiarity with CI/CD pipelines and version control systems
  </li>
  <li>
   Excellent problem-solving, analytical, and communication skills
  </li>
  <li>
   Hands-on experience with JMeter for performance testing and Postman for API testing
  </li>
  <li>
   Expertise in test case design and execution using structured approaches
  </li>
  <li>
   Proficiency in multi-platform testing (Android, iOS, and Websites)
  </li>
  <li>
   Familiarity with automation tools (Appium, Selenium, or similar) will be considered a strong plus
  </li>
  <li>
   Ability to work independently and collaboratively within cross-functional teams
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   About MMBL:
  </strong>
 </p>
 <p>
  Mobilink Microfinance Bank Ltd. is providing banking services to over 48 million registered users including 20+ million monthly active customers across Pakistan. With a hybrid model that combines traditional microfinance with mobile/digital banking technologies, the bank now operates with over 114 branches and 270,000 branchless banking agents and provides a USSD (GSM) based digital channel offering savings, micro enterprise (MSME) loans, small housing loans, remittances, collection (utility bills and loan instalments), mobile wallets, insurance, G2P, B2B &amp; B2P payments; thus, playing a leading role in the promotion of financial inclusion. MMBL is committed to fostering a positive and productive workplace, and our core values reflect this focus. These values include promoting innovation and entrepreneurship, encouraging teamwork and collaboration, and prioritizing a customer-centric approach in all aspects of our business.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Why Join MMBL?
  </strong>
 </p>
 <p>
  This is an opportunity for someone who is passionate about making a difference and playing a key role in driving transformative change. Our team is committed to empowering millions with the tools necessary to succeed in the digital age, and we're looking for a talented individual to join us in this endeavour.
 </p>
</div>


Assistant Manager, QA Automation

Macquarie Group

<div><div><div><div><div><div><div><div><div><div><div>We have an exciting opportunity to join our dynamic and agile People and Culture technology team. We are comprised of Full Stack Engineers with deep expertise, as well as broad understanding of related disciplines in engineering.</div></div><br>
</div></div><div><div><div>At Macquarie, our advantage is bringing together diverse people and empowering them to shape all kinds of possibilities. We are a global financial services group operating in 31 markets and with 56 years of unbroken profitability. You&rsquo;ll be part of a friendly and supportive team where everyone - no matter what role - contributes ideas and drives outcomes.</div>
</div></div></div></div></div><div><div><div><div>What role will you play?</div></div><div><br>
</div></div><div><div><div><div><div><div>In this role, you will drive testing and automation initiatives to deliver a seamless, end-to-end digital experience across our ecosystem. Your expertise will help shape innovative, and high-quality solutions in a dynamic environment.</div></div><br>
</div></div></div></div></div><div><div><div><div>What you offer</div></div><div><br>
</div></div><p></p><div><div><div><div><ul><li>Proven expertise in testing HR platforms, with a proactive and detail-oriented approach</li><li>
Design and develop automated test frameworks to validate functionality, performance, and security</li><li>
Collaborate with cross-functional teams (application administrators, software engineers, and business analysts) to refine test cases and develop robust test plans</li><li>
Provide thought leadership to enhance Quality Engineering practices, championing continuous improvement and best practices</li><li>
Thrive in a collaborative, agile environment, driving quality and innovation in application and platform testing</li></ul><br>
</div></div><div><div><div>We love hearing from anyone inspired to build a better future with us, if you're excited about the role or working at Macquarie we encourage you to apply.</div>
</div></div></div></div></div><div><div><div><div>What we offer</div></div><div><br>
</div></div><div><div><div><div><p>At Macquarie, you&rsquo;re empowered to shape a career that&rsquo;s rewarding in all the ways that matter most to you. Macquarie employees can access a wide range of benefits which, depending on eligibility criteria, include:</p><br>
<ul><li>
1 wellbeing leave day per year</li><li>
26 weeks&rsquo; paid maternity leave or 20 weeks&rsquo; paid parental leave for primary caregivers along with 12 days of paid transition leave upon return to work and 6 weeks&rsquo; paid leave for secondary caregivers</li><li>
Company-subsidised childcare services</li><li>
2 days of paid volunteer leave and donation matching</li><li>
Benefits to support your physical, mental and financial wellbeing including comprehensive medical and life insurance cover, the option to join parental medical insurance plan and virtual medical consultations extended to family members</li><li>
Access to our Employee Assistance Program, a robust behavioural health network with counselling and coaching services</li><li>
Access to a wide range of learning and development opportunities, including reimbursement for professional membership or subscription</li><li>
Hybrid and flexible working arrangements, dependent on role</li><li>
Reimbursement for work from home equipment</li></ul>
</div></div></div></div></div><div><div><div><div>About Technology</div></div><div><br>
</div></div><div><div><div><div><div>Technology enables every aspect of Macquarie, for our people, our customers and our communities. We&rsquo;re a global team that is passionate about accelerating the digital enterprise, connecting people and data, building platforms and applications and designing tomorrow&rsquo;s technology solutions.</div>
</div></div></div></div></div><div><div><div><div>Our commitment to diversity, equity and inclusion</div></div><div><br>
</div></div><div><div><div><div><div>We are committed to fostering a diverse, equitable and inclusive workplace. We encourage people from all backgrounds to apply and welcome all identities, including race, ethnicity, cultural identity, nationality, gender (including gender identity or expression), age, sexual orientation, marital or partnership status, parental, caregiving or family status, neurodiversity, religion or belief, disability, or socio-economic background. We welcome further discussions on how you can feel included and belong at Macquarie as you progress through our recruitment process.<div><div><br>
Our aim is to provide reasonable adjustments to individuals who may need support during the recruitment process and through working arrangements. If you require additional assistance, please let us know in the application process.</div></div></div></div></div></div></div></div></div></div></div></div>

Manager | QA Engineer

Alvogen

<p></p><div><div><p><b>SUMMARY OF POSITION</b></p></div><p><br>
The QRM (Quality Relationship Manager) Technical Services is a member of the US Quality department. In this position, the QRM will be interacting primarily with Alvogen&rsquo;s external business partners/CMOs. The incumbent will have responsibility for mainly managing products from development to product launch and commercial phase as assigned. QRM is responsible for supporting the technical aspects of the products as well as the adherence to Alvogen&rsquo;s Quality Management System. The position will require in depth knowledge of Quality Systems including activities such as development, validation, troubleshooting/ investigation support, complaint handling, change control, product release, inspection support, etc. The individual will also support the technical transfer of products to/from various CMO&rsquo;s. The individual serves as a critical link to Alvogen&rsquo;s external partners. Being able to effectively communicate and transmit information to/from partners is essential to ensure compliance and optimal performance.</p><p></p><p><b><br>
ORGANIZATION STRUCTURE</b></p><p><br>
The QRM Tech. Services reports directly to the Director Quality, Commercial and Technical Services, Third Party Quality US. There are no reports.</p><p></p><p><b><br>
RESPONSIBILITIES</b></p><p>
Primary responsibilities of this role include, but are not limited to, the following:</p><br>
<p></p><ul><li>
Documentation Review &amp; Approval:</li><li>
Review and approve documentation such as Method Validations, Manufacturing Records, SOPs, Investigations, Change Controls, Validation Reports, Technical reports required for regulatory filing, including but not limited to Extractables/ Leachable studies, Nitrosamine Reports etc, Equipment Qualifications and similar documents as directed by Quality Management.</li><li>
Inspections and Audits:</li></ul><ul><li>
Prepare / Support preparation activities for regulatory inspections</li><li>
Evaluate regulatory agency findings from inspections conducted at CMOs/CPOs/analytical Laboratories, etc.</li></ul><ul><li>
Support the design and implementation of system / process improvements where opportunities are identified (Commercial &amp; Development), including associated CAPA&rsquo;s.</li><li>
Support technical transfer / validation activities with external business partners / CMOs.</li><li>
Manage the Finished Product / Bulk Drug Product ANDA/NDA, Launch Release System:</li></ul><ul><li>
Execute the Alvogen Inc. and Almatica Pharma Inc. material release procedure(s). Manage ANDA/NDA, launch release priorities per business deadlines. Work directly with CMOs and partners to resolve related questions/issues.</li><li>
File, retrieve, and maintain organized records</li></ul><br>
<p></p><ul><li>
Communicate with external business partners / CMOs regarding quality related issues and Quality Agreements.</li><li>
Provide investigation/trouble-shooting support as needed. Review and approve investigations, unexplained discrepancies, failures, and out-of-specification results. Evaluate if there is any quality impact to process/product and take appropriate action.</li><li>
Track metrics for external business partners / CMOs on change controls, deviations, complaints, audits, product releases and rejections and other Third-Party Quality Key Performance Indicators.</li><li>
Change Management Program:</li></ul><ul><li>
Process change controls for all systems requiring change control support (e.g. specifications for raw materials, drug product intermediates and finished drug products, validation protocols and reports, master production and packaging records, cleaning records, and analytical methods).</li><li>
Maintain change control electronic records in EQMS.</li><li>
Review, assess, and approve change controls as required by SOP&rsquo;s.</li><li>
Support training of company personnel on change control system.</li></ul><ul><li>
Support the corporate Training Program, when / if needed.</li><li>
Support the corporate audit program as needed / required.</li><li>
Keeps abreast of industry regulations and cGMP trends. Stays informed of FDA and ICH Guidelines related to GMP (Commercial &amp; Development).</li></ul><p></p><div><p><b><br>
QUALIFICATIONS</b></p></div><p><br>
Position requires the following education and qualification prerequisites:</p><br>
<p></p><ul><li>
Good leadership skills in all areas of communication, influencing, collaboration and decision-making.</li><li>
BS in Pharmacy, Chemistry, Microbiology or Biology with a minimum of 10 years&rsquo; experience in the Pharmaceutical Industry preferred. Other degrees will be considered based on extensive industry experience.</li><li>
Experience in GxP laboratory practices.</li><li>
Release of materials and products supporting both development and commercial activities.</li><li>
Has knowledge of GxP quality systems, US FDA regulations and ICH guidance documents.</li><li>
Experience with various manufacturing / filling processes associated with &lsquo;non-sterile&rsquo; drug products.</li><li>
Demonstrated experience supporting deviations, investigations especially, OOS investigations. Experience in conducting, writing/reviewing deviations and investigations, root cause analyses, and identifying corrective actions. Must have strong technical knowledge of FDA and other regulatory guidance and be able to critically review complex investigations, interpret results and able to evaluate technical input against compliance requirements in line with CFR requirements and other regulatory requirements and Alvogen procedures/policies.</li><li>
Must hold strong interpersonal and communication skills. Must have the ability to work well with diverse groups including the ability to work in a team environment. Must also display strong organizational skills with the ability to lead team meetings and to manage multiple projects at one time.</li><li>
Strong technical writing and computer skills are also required.</li><li>
Must display the ability to work independently with little or no supervision and plan and accomplish set goals.</li></ul><p></p><p><br>
Physical Demand Factors</p><br>
<p></p><ul><li>
While performing the duties of this job, the QRM Tech. Services is required to sit and work at a computer for extended periods of time.</li></ul><br>
<p></p><ul><li>
Is regularly required to talk, listen, and attend meetings / teleconference calls.</li><li>
Approximately 20% business travel required to external Contract Manufacturing Organization (CMO) / Business Partner sites, or to attend professional development training seminars &ndash; as needed / directed.</li></ul><p></p><p><b><br>
GMP DECISION-MAKING AUTHORITY</b></p><p><br>
Independent decision-making activities will be performed by the QRM Tech. Services for all the quality management system elements outlined in the Responsibilities section of this Job Description.</p><p></p><p><i><br>
The anticipated base salary range for this position is $100,000-$135,000. This position is eligible for Alvogen&rsquo;s annual discretionary bonus and comprehensive benefits package, consisting of medical and prescription drug coverage (two PPO plans and an HDHP with Health Savings Account and employer contribution), dental, vision, flexible spending accounts. Alvogen&rsquo;s benefits package also includes a retirement savings program, long-term care coverage, paid time off (176 hours per year, prorated to hire date) inclusive of sick time, disability benefits, life insurance, a wellness program, and 13 company recognized paid holidays per year. We anticipate this position will be posted on March 19, 2026 and remain open for at least 30 days. To apply, select the apply button and submit your application.</i></p><p></p><p><b><br>
An Equal Opportunity Employer, including disability/vets.</b></p></div><p></p>

Quality Relationship Manager, QA Tech Service

Asteco

<div>
 <p>
  <strong>
   Title:
  </strong>
  QA Assistant Manager
 </p>
 <p>
  <strong>
   Reports to:
  </strong>
  QA Vice-President
 </p>
 <p>
  <strong>
   Division:
  </strong>
  QA
 </p>
 <p>
  <strong>
   Department:
  </strong>
  PDD
 </p>
 <p>
  <strong>
   Location:
  </strong>
  Site Office
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Job Purpose
  </strong>
 </p>
 <p>
  The Quality Assistant Manager leads and supports the QA team on-site by ensuring daily tasks are assigned and inspections are carried out effectively. They report to the QA Manager and communicate issues to higher management.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Roles, Responsibilities, Duties
  </strong>
 </p>
 <ul>
  <li>
   Set up the onsite platform for new projects and ensure all workflows and necessary project details are provided.
  </li>
  <li>
   Lead the QA team on a daily basis, assigning tasks and ensuring each team member is clear on their duties and responsibilities.
  </li>
  <li>
   Ensure the QA team has access to the necessary tools and equipment for inspections and manage the availability of these resources.
  </li>
  <li>
   Maintain and update the asset register log to track tools, equipment, and other resources used for inspections and quality assurance tasks.
  </li>
  <li>
   Assist in carrying out internal audits twice per project life cycle to assess compliance with quality standards and identify areas for improvement.
  </li>
  <li>
   Ensure all scheduled inspections and quality assurance tasks are completed on time and as agreed upon.
  </li>
  <li>
   Communicate technical quality issues to the QA Manager and Head of Department for timely resolution.
  </li>
  <li>
   Report significant quality issues to the broader project team to ensure major concerns are addressed.
  </li>
  <li>
   Develop and submit weekly progress reports to track the status of quality inspections, audits, and related activities.
  </li>
  <li>
   Ensure that the onsite quality management system is fully utilized across all projects.
  </li>
  <li>
   Maintain accurate records of inspections, audits, and other quality-related activities.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <p>
  <strong>
   Education
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Civil Engineering, Architecture, or a related field.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Experience &amp; Skills
  </strong>
 </p>
 <p>
  <strong>
   Required Technical Skills
  </strong>
 </p>
 <ul>
  <li>
   Minimum 10 years of experience in QA/QC, construction supervision, or property handover in the UAE.
  </li>
  <li>
   Strong understanding of building finishes, MEP systems, and integrated QA processes.
  </li>
  <li>
   Proficient in snagging platforms and reporting systems.
  </li>
  <li>
   Familiarity with regulatory bodies and handover compliance procedures.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Personal &amp; Soft Skills
  </strong>
 </p>
 <ul>
  <li>
   Strong leadership with the ability to manage a multi-disciplinary team.
  </li>
  <li>
   Excellent planning and workload management across parallel projects.
  </li>
  <li>
   High attention to detail with strategic problem-solving capability.
  </li>
  <li>
   Resilient under pressure, especially during peak handover periods.
  </li>
  <li>
   Strong communication and stakeholder management skills.
  </li>
  <li>
   Customer-focused with the ability to manage expectations diplomatically.
  </li>
 </ul>
 <p>
 </p>
</div>


Assistant Manager - Property QA/QC Engineer

Mashreq

<div>
 To support the QA &amp; Proofing function by executing day-to-day quality assurance activities, validating reconciliation proofing submissions, tracking escalations, and identifying gaps in data or process adherence. The role ensures consistent implementation of the control framework across group operations and contributes to continuous process improvements, working closely with first-line ops and GRC.
</div>


Assistant Manager - QA & Proofing Unit.COE Pak - Ops-Operations GRC.Operations Group-PAKCOE

SoftSquare

<div>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 Job Description
 <br/>
 <br/>
 <ul>
  <li>
   Create test plans, maintain documentation and perform testing on multiple devices, platforms, and browsers;
  </li>
  <li>
   Performance testing experience in JMeter including API testing;
  </li>
  <li>
   Use one or more Testing Automation Frameworks: Detox, Cypress, Appium, Robotium, Selenium, Cucumber;
  </li>
  <li>
   Cover all the phases of QA testing: System (functional and non-functional), Integration, Regression, Smoke, Exploratory, Performance, Data verification and Acceptance testing;
  </li>
  <li>
   Work and Coordinate with Team lead, Project manager, and Business analyst.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Requirements
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Knowledge of Agile methodologies, SCRUM, and Agile Testing Life Cycles
  </li>
  <li>
   Experience in both manual testing and automation;
  </li>
  <li>
   Knowledge of Software quality (SQA) methodologies and practices;
  </li>
  <li>
   1-2 years of experience in working in quality assurance department;
  </li>
  <li>
   Bachelor&rsquo;s degree in BS-CS, BE, BIS from a reputed university;
  </li>
  <li>
   Must have strong problem solving skills &amp; result oriented, self-drive, ability to complete project / assign tasks without follow-up;
  </li>
  <li>
   Desire to keep on learning and growing.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Job Type:
 </strong>
 Full-time
 <br/>
 <br/>
 <strong>
  Ability to commute/relocate
 </strong>
</div>


SQA Executive

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