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clinical trials quality assurance associate (night) Jobs in Karachi

clinical trials quality assurance associate (night)

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quality assurance specialist

Plutus21

<div><h3 class="jobSectionHeader">Job Title: Research Quality Assurance Lead</h3><h3 class="jobSectionHeader">
About the Role</h3>
At Plutus21 Capital, rigorous research is at the core of our investment strategy. The Research Quality Assurance (QA) Lead ensures that every report, model, and memo reflects the firm&rsquo;s standards of precision, clarity, and investor relevance. This role is both editorial and analytical, combining a sharp eye for detail with strong investment literacy.<h3 class="jobSectionHeader">
Key Responsibilities</h3><ul><li>
Write, edit, and review research reports to ensure they meet professional and investor-ready standards.</li><li>
Maintain consistency of tone, structure, and messaging across all research and company-wide outputs.</li><li>
Develop and implement QA frameworks for research outputs, data models, and investment memos.</li><li>
Collect, maintain, and structure large financial, blockchain, and macroeconomic datasets</li><li>
Review research for methodological soundness, statistical rigor, and data integrity.</li><li>
Coordinate with analysts and researchers to provide structured feedback and ensure revisions are addressed.</li><li>
Maintain version control and documentation standards across research products.</li><li>
Establish best practices for reproducibility, citation, and data governance.</li></ul><h3 class="jobSectionHeader">
Qualifications</h3><ul><li>
Master&rsquo;s degree in Economics, Finance, Data Science, or related discipline (PhD preferred).</li><li>
4+ years of experience in research management, editorial oversight, or data auditing.</li><li>
Strong understanding of econometrics, data pipelines, and financial analysis.</li><li>
Experience with reproducibility tools (Git, Jupyter, LaTeX, etc.) is a plus.</li></ul>
Detail-oriented mindset with ability to enforce high standards.</div>

Research Quality Assurance Lead

Eminent4U

About the Role:We are seeking a dedicated Quality Assurance Executive to join our dynamic team. This role is crucial for maintaining the highest standards of service quality and compliance within our Call Centre operations, regulated by the Financial Conduct Authority (FCA). You will play a pivotal role in assessing and enhancing the performance of our Call Centre associates, ensuring our services not only meet but exceed regulatory standards and customer expectations.Responsibilities:<ul><li>Quality Assurance and Compliance Monitoring:</li></ul>Conduct thorough assessments of all FCA-regulated protocols to ensure the quality and compliance of interactions between Call Centre associates and customers.<ul><li>Call Monitoring:</li></ul>Systematically monitor both inbound and outbound calls to verify technical accuracy and conformity with the company's policies and procedures. Manage and book large volumes of calls, manually dial customers and subcontractors for appointments, and rearrange or swap engineers' jobs while updating customers accordingly.<ul><li>Team Management:</li></ul>Efficiently manage team groups to provide prompt feedback &amp; stats to our customer facing agent and relevant supervisors to increase the efficacy &amp; to increase their experience on customer journey.<ul><li>Administrative Duties:</li></ul>Perform necessary administrative tasks, including updating and logging sheets as assigned by colleagues.We Value:<ul><li>Minimum 1 year of experience in a similar role.</li><li>Excellent verbal, written, and interpersonal communication skills.</li><li>Exceptional listening and analytical skills.</li><li>Strong time management skills.</li><li>Ability to multi-task and successfully operate in a fast-paced, team environment.</li><li>Must adapt well to change and successfully set and adjust priorities as needed.</li><li>Proficiency in Microsoft Word &amp; Excel.</li></ul>Why Join Eminent4U?<ul><li>Shifts: Daytime 01:00 pm till 09:30 pm PST with alternate weekends off.</li><li>Market Competitive along with KPI based rewards, Punctuality allowance, Weekday allowance, Birthday allowance, Annual Bonuses, Anniversary Bonus &amp; several other fringe benefits.</li><li>Opportunity to work in a dynamic and inclusive environment focused on professional growth and employee satisfaction.</li></ul>Location: Shahra-e-Faisal, PECHS, Block-6, KarachiJob Type: Full-timePay: Up to Rs70,000.00 per monthApplication Question(s):<ul><li>Can you join us urgently?</li></ul>Experience:<ul><li>Calls Quality Assurance: 1 year (Required)</li></ul>Language:<ul><li>English (Preferred)</li></ul>Work Location: In person

Quality Assurance Executive (Calls)

RED CORAL SERVICES

Job Description:Red Coral Services is seeking a highly motivated Software Quality Assurance (SQA) Engineer to join our dynamic team. As an SQA Engineer, you will play a crucial role in ensuring the quality and reliability of our software applications. If you are passionate about delivering high-quality software, have experience in ecommerce platforms, and enjoy collaborating with cross-functional teams, we invite you to apply for this exciting opportunity.Responsibilities:<ul><li>Collaborate with cross-functional teams to understand software requirements and specifications.</li><li>Design, develop, and execute test plans and test cases for software applications.</li><li>Conduct thorough testing to ensure software functionality, reliability, performance, and security meet quality standards.</li><li>Identify and report software defects, working closely with development teams to ensure timely resolution.</li><li>Perform regression testing to validate software changes and updates.</li><li>Participate in the continuous improvement of testing processes and methodologies.</li><li>Stay up-to-date with industry best practices and emerging trends in software quality assurance.</li></ul>Qualifications:<ul><li>Bachelor's degree in Computer Science, Engineering, or related field.</li><li>Proven experience OF 2 Years as a software QA Engineer worked on e-commerce preferred.</li><li>Strong understanding of software testing methodologies and processes.</li><li>Experience with test automation tools and frameworks.</li><li>Proficiency in programming/scripting languages (e.g., C#, Java, Database).</li><li>Excellent communication and collaboration skills.</li><li>Attention to detail and a passion for delivering high-quality software.</li><li>Must have knowledge of ecommerce platforms and their specific testing requirements.</li></ul>To apply, please submit your resume to madiha.shahid@redcoralservice.com with the subject line &ldquo;SQA ENGINEER&rdquo;.Job Type: Full-timeWork Location: In person

Software Quality Assurance

Strugbits (PVT.) LTD

Strugbits is looking for a talented and detail-oriented Quality Assurance Engineer to join our team!Key Responsibilities:<ul><li>Develop, document, and execute test plans and test cases for web and mobile applications.</li><li>Identify, log, and track software defects to resolution.</li><li>Collaborate with development teams to understand project requirements and ensure thorough testing coverage.</li><li>Perform functional, regression, and usability testing.</li><li>Provide feedback to enhance the quality and usability of applications.</li><li>Continuously improve QA processes and methodologies.</li></ul>Requirements:<ul><li>Bachelor&rsquo;s degree in Computer Science, Software Engineering, or a related field.</li><li>Minimum 3 year of experience in software testing and quality assurance.</li><li>Strong understanding of QA methodologies, tools, and processes.</li><li>Proficiency in manual testing (automation experience is a plus).</li><li>Excellent analytical and problem-solving skills.</li><li>Good communication skills to collaborate effectively with the team.</li></ul>Location: Gulshan-e-Iqbal, KarachiWork Timing: 12:00 PM to 9:00 PMJob Type: Full-timePay: Rs50,000.00 - Rs80,000.00 per monthEducation:<ul><li>Bachelor's (Required)</li></ul>Experience:<ul><li>Manual Testing : 3 years (Required)</li></ul>Work Location: In person

Sofware Quality Assurance Engineer

Minerva Research Solutions

<div>
 
 JOB DESCRIPTION:
 
 
 
 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.
 
 
 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.
 
 
 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.
 
 
 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.
 
 
 
 Responsibilities:
 
 
 
 <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>
 
 Knowledge, Education, and Experience:
 
 
 
 <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>
 
 Skills and Abilities:
 
 
 
 <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>
 
 Benefits:
 
 
 
 <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>
 
 Openings:
 
 
 
 04 positions
 
 
 Full-time
 
 
 On-site job
 
 
 
 Work Schedule Timings:
 
 
 
 Monday to Friday
 
 
 Evening Shift (07 PM to 03 AM)
 
 
 (transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
 
 
 Powered by JazzHR
 
 
 5xFcDQcNex
</div>

Clinical Trials Quality Assurance Associate (Night)

<div>JOB DESCRIPTION: 
 
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.
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. 
 
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. 
 
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.
Responsibilities:<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>
Knowledge, Education, and Experience:<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>
Skills and Abilities:<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>
Benefits:<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>
Openings:
04 positions 
Full-time 
On-site job 
 
Work Schedule Timings: 
Monday to Friday 
Evening Shift (07 PM to 03 AM) 
(transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
5xFcDQcNex</div>

MUJTABA TEXTILES

To ensure that all textile products meet defined quality standards, customer specifications, and regulatory requirements by implementing, monitoring, and improving quality control processes across all stages of production.Key Responsibilities:1. Quality Control &amp; Inspection2. Process Monitoring &amp; Compliance3. Reporting &amp; Documentation4. Problem Solving &amp; Corrective Action5. Continuous ImprovementKey Skills &amp; Competencies:<ul><li>Strong knowledge of textile processes (weaving, Dyeing, Printing, finishing, stitching).</li><li>Familiar with international quality standards (AQL, ISO, ASTM, etc.).</li><li>Good problem-solving and analytical skills.</li><li>Attention to detail and strong observation skills.</li><li>Effective communication and reporting abilities.</li><li>Proficiency in MS Office.</li></ul>Job Type: Full-timeEducation:<ul><li>Bachelor's (Preferred)</li></ul>Experience:<ul><li>Quality Assurance: 3 years (Required)</li></ul>Work Location: In person

Quality Assurance Officer (Textile Industry)

Explore 934+ Quality assurance specialist in Karachi this October. Find roles across top companies and apply now to boost your career.

934 quality assurance specialist jobs IN Karachi

Research Quality Assurance Lead

Quality Assurance Executive (Calls)

Software Quality Assurance

Sofware Quality Assurance Engineer

Clinical Trials Quality Assurance Associate (Night)

Clinical Trials Quality Assurance Associate (Night)

Quality Assurance Officer (Textile Industry)