clinical trials quality assurance associate (night) Jobs in Karachi

clinical trials quality assurance associate (night)

ar specialist i/ii

consultant qa, qc

customer services specialist Jobs in Karachi

customer services specialist

manager sqa - i

quality assurance specialist

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)
TuBXaWOaue</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)
 
 
 Powered by JazzHR
 
 
 TuBXaWOaue
</div>

The BranPac

The BranPac is on the lookout for a Quality Assurance Executive with a strong fashion background and hands-on experience in Shopify and eCommerce brands. If you&rsquo;re passionate about fashion, detail-oriented, and know how to keep online experiences seamless and stylish &mdash; we&rsquo;d love to have you on board.Key Responsibilities:<ul><li>Conduct quality checks on all Shopify product listings &mdash; ensuring accuracy in titles, descriptions, pricing, and imagery.</li><li>Test website functionality and report bugs, broken links, or visual inconsistencies.</li><li>Collaborate with design, content, and eCommerce teams to maintain consistent brand presentation across digital platforms.</li><li>Audit product data, size charts, and metadata for alignment with fashion brand standards.</li><li>Review campaign launches, product uploads, and content updates to ensure flawless execution.</li><li>Support continuous improvement by suggesting process enhancements and QA best practices.</li></ul>Requirements:<ul><li>Bachelor&rsquo;s degree in Fashion, Business, Marketing, or a related field.</li><li>Proven experience (1&ndash;2 years) in quality assurance, eCommerce, or fashion retail operations.</li><li>Hands-on experience with Shopify (store management, testing, and updates).</li><li>Solid understanding of online customer experience, product display, and merchandising standards.</li><li>Strong analytical skills and keen attention to detail.</li><li>Ability to work collaboratively in a fast-paced creative environment.</li></ul>What We Offer:Competitive salary packageExposure to leading luxury fashion, fast fashion, jewellery, make-up, skin care and lifestyle brandsCollaborative and creative work cultureGrowth opportunitiesJob Type: Full-timeWork Location: In person

Quality Assurance Executive

Centric Brands

<div>
 
 About Us
 
 
 
 Centric Brands is a leading lifestyle brand collective that designs, sources, markets and sells high quality products in multiple segments, including women&rsquo;s, men&rsquo;s and kid&rsquo;s apparel, accessories, entertainment and beauty. Centric Brands is focused on our customers and our brands that will drive the company&rsquo;s future growth. We are defined by innovation as we seize new opportunities and thrive in an environment informed by creativity and thinking that is both analytical and outside the box. Centric Brands reflects a team built on respect, for others and for the hard work it takes to achieve our goals and build our bright future together.
 
 
 
 Specific Responsibilities Would Include
 
 
 
 <ul>
 <li>
 Primary Responsibilities: Quality Assurance function in Pakistan
 </li>
 <li>
 Coordination of Fit, PP approval, PP meeting.
 </li>
 <li>
 Conduct Inline inspections, Final inspections.
 </li>
 <li>
 Follow up on Production WIP and report any challenges communicate to Asia Leads/NA Leads.
 </li>
 <li>
 Communicate inspection results for each production order with Head office
 </li>
 <li>
 Conduct full packaging inspection of components, execution, and stickers
 </li>
 <li>
 Preparation and communication of daily quality inspection.
 </li>
 <li>
 WIP maintenance and Tracking
 </li>
 <li>
 Any Licensor/Customer QA w/Factories inclusive of packing instructions
 </li>
 <li>
 Factory Audits and Corrective Action Plan
 </li>
 <li>
 Tracking of Color, Bulk Fabric &amp; Trim Approval
 </li>
 <li>
 Samples &amp; Special Req&rsquo;s- PD and Design
 </li>
 <li>
 QA w/Factories inclusive of packing instructions
 </li>
 <li>
 Report Review and support in problem resolution
 </li>
 <li>
 Compliance. On-boarding and Corrective Action
 </li>
 <li>
 Collaborator of Vendor Allocation and Sourcing Strategy
 </li>
 <li>
 Checking and sending official PO to factory &amp; update delivery date on SAP.
 </li>
 <li>
 Coordinate with sales for the QTY/Delivery/direct shipment order Booking issue on HFC/CPO/PO
 
 
 </li>
 </ul>
 
 Our Best Fit Candidate Would Have
 
 
 
 <ul>
 <li>
 Proven working experience in quality assurance / textile field
 </li>
 <li>
 Creativity, technical capability and sensibility for garment / textile
 </li>
 <li>
 Up to date with the latest QA /QC and best practices
 </li>
 <li>
 Knowledge of garment manufacturing, including construction, fabrication, trim and print techniques
 </li>
 <li>
 Ability to multi-task and meet deadlines; highly detail oriented and meticulous
 </li>
 <li>
 Bachelor&rsquo;s Degree in Textile or related field
 </li>
 <li>
 Excellent verbal and written communications skills
 </li>
 <li>
 Proficient in Microsoft Office, Adobe products, Excel
 
 
 </li>
 </ul>
</div>

Consultant QA, QC

Safa Worldwide Private Limited

PLEASE NOTE! NOT ANSWERING QUESTIONS WILL RESULT IN DIRECT REJECTION OF APPLICATION EVEN IF YOU HAVE RELEVANT EXPERIENCE. Job Title: Quality Assurance Officer &ndash; Outbound Sales CallsAbout the RoleWe are looking for a Quality Assurance (QA) Officer to monitor, evaluate, and enhance the performance of our International Sales Representatives who engage with UK-based clients. The QA Officer will play a critical role in maintaining service excellence by ensuring all outbound calls meet the company&rsquo;s communication, compliance, and customer experience standards.You will be responsible for reviewing recorded sales calls, providing feedback, identifying training needs, and supporting continuous improvement across the sales team.Responsibilities:<ul><li>Monitor and evaluate outbound sales calls for quality, accuracy, compliance, and customer engagement standards.</li><li>Assess call recordings to ensure adherence to scripts, sales processes, and company policies.</li><li>Provide constructive feedback and coaching to sales representatives to improve performance and communication effectiveness.</li><li>Develop and maintain QA scorecards, evaluation criteria, and performance reports.</li><li>Identify common issues or gaps in call handling and recommend process improvements.</li><li>Collaborate with Sales Managers and Trainers to align quality standards with sales goals and training programs.</li><li>Ensure that all representatives maintain a professional tone, clear English communication, and ethical sales practices.</li><li>Support management during monthly performance reviews by sharing insights and quality reports.</li><li>Maintain confidentiality of all monitored communications and sensitive customer data.</li><li>Excellent interpersonal skills and the ability to thrive in a team environment</li></ul>What We Offer:<ul><li>Competitive salary: PKR 60,000 &ndash; 75,000+ Commissions (based on experience)</li><li>Ongoing professional development and growth opportunities</li><li>Monthly performance reviews for career advancement</li><li>Supportive, collaborative, and employee-focused work culture</li></ul>Working Hours:<ul><li>Monday &ndash; Friday: 2:00 PM &ndash; 11:00 PM</li><li>Saturday: 2:00 PM &ndash; 8:00 PM (Half-day)</li></ul>Additional Details:<ul><li>Job Type: Full-Time | Office-Based</li><li>Compensation: PKR 60,000 &ndash; 75,000 + Commissions per month</li><li>Location Requirement: Must be based in Karachi</li></ul>Job Type: Full-timePay: Rs60,000.00 - Rs75,000.00 per monthApplication Question(s):<ul><li>Briefly mention the campaigns you have worked in before?</li><li>Do you have on call INTERNATIONAL SALES experience in a call centre?</li><li>What's your age?</li><li>What's your residential area?</li><li>Can you manage your own transport to DHA Ph 6 chota shahbaz commercial daily?</li><li>What are you basic salary expectations?</li><li>What was your last salary?</li><li>Do you have OA levels background?</li><li>Are you employed or unemloyed? (if employed, how long is your notice period)?</li></ul>Work Location: In person

QA Officer – Sales Calls

Explore 752+ Quality assurance specialist in Karachi this November. Find roles across top companies and apply now to boost your career.

752 quality assurance specialist jobs IN Karachi

Software Quality Assurance

Sofware Quality Assurance Engineer

Clinical Trials Quality Assurance Associate (Night)

Clinical Trials Quality Assurance Associate (Night)

Quality Assurance Executive

Consultant QA, QC

QA Officer – Sales Calls