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assistant manager supplier quality assurance Jobs in Karachi

assistant manager supplier quality assurance

quality assurance specialist

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
 
 
 oBYUMSP7Bw
</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
 
 
 64zzPpFqpi
</div>

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

SOC Solutions LLC

Botmer International is Hiring: Senior QA Engineer (12 PM to 9 PM PKT)Botmer International is expanding, and we are looking for a skilled Senior QA Engineer to lead quality assurance across our AI, mobile, and web projects. This role requires someone who takes ownership, communicates clearly, and ensures every release meets high standards.Position: Senior QA EngineerTiming: 12 PM to 9 PM PKT (US overlap) Location: Karachi (On-site)Responsibilities<ul><li>Lead QA efforts across multiple ongoing projects.</li><li>Create and execute test plans, test cases, and automated test scripts.</li><li>Perform functional, regression, integration, and performance testing.</li><li>Identify bugs, document clearly, and follow through until resolution.</li><li>Collaborate closely with engineering, product, and design teams.</li><li>Improve QA processes, automation, and overall product stability.</li></ul>Requirements<ul><li>Minimum 3 years of QA experience (manual and automation).</li><li>Strong understanding of SDLC, STLC, and QA best practices.</li><li>Hands-on experience with Selenium, Postman, JIRA, JMeter, or similar tools.</li><li>Ability to write clear test documentation and bug reports.</li><li>Strong communication skills and ownership mindset.</li><li>Experience in a fast-paced software agency or product environment is a plus.</li></ul>Preferred Skills<ul><li>API testing</li><li>Mobile app testing</li><li>Automation frameworks (Cypress, Playwright, Selenium)</li><li>CI/CD familiarity</li></ul>What We Offer<ul><li>Competitive salary based on experience</li><li>Opportunity to work with global clients</li><li>Fast-paced environment with growth potential</li><li>Work alongside AI, product, and engineering teams</li></ul>Job Type: Full-timePay: Rs100,000.00 - Rs150,000.00 per monthApplication Question(s):<ul><li>Can you join immediately?</li><li>What is your expected salary for this role? We're currently offering between 100K to 150K PKR per month based on expertise and years of experience.</li></ul>Experience:<ul><li>Software Quality Assurance Testing: 3 years (Required)</li></ul>Work Location: In person

Software Quality Assurance Engineer

Intelligenes

We are looking for a &lsquo;Software Quality Assurance Engineer - Mid Level&rsquo;. The ideal candidate should possess the following:Job Description<ul><li>Participate in requirements review and understand new feature development.</li><li>Assist in designing, implementation and execution of test cases for new and existing features.</li><li>Collaborate with software engineering team on QA/Testing topics.</li><li>Perform UI/UX testing to uncover flaws within the interface.</li><li>Contribute to our quality projects, including automation of test cases, with a focus on feature deployment</li><li>Actively participates in agile meetings with product management and development team</li><li>Gather requirements, build testing solutions and troubleshoot issues in order to deliver high-quality projects &amp; products.</li><li>Communicate technical concepts/issues clearly to internal stakeholders</li><li>Develops, documents and maintains test cases and validation reports.</li><li>Learn how to automate</li><li>Learn and develop QA best practices</li><li>Identify and communicate risks</li><li>Has knowledge of Azure DevOps</li><li>Has basic idea of SQL queries</li></ul>Minimum Education: Bachelors (Computer Engineering, Software Engineering and Computer Science)Experience Required: Minimum 2 &ndash; 4 years of experience in the similar role.Employment Benefits:<ul><li>Market competitive salary package</li><li>Hybrid Working</li><li>Medical coverage</li><li>OPD Allowance</li><li>Travel Allowance</li><li>Bi-Annual Increments</li><li>Performance-Based Quarterly Rewards</li></ul>Job Type: Full-timeWork Location: In person

Mid Level Software Engineer – Quality Assurance

<div><div>You will provide quality oversight on the production floor to help ensure safe, compliant and timely supply. You will work closely with production, engineering, laboratory and other teams to identify and resolve quality issues in real time. We value curiosity, clear communication and practical problem solving. This role offers hands-on experience, learning and career growth while contributing to GSK&rsquo;s mission of uniting science, technology and talent to get ahead of disease together.
 
 
Responsibilities
 
<ul><li>Perform in-process checks during manufacturing, filling and packaging to ensure procedures and specifications are followed.
</li><li>Support investigations into deviations, incidents and customer complaints and help implement corrective and preventive actions.
</li><li>Assist in review and compilation of batch records to support timely and compliant product release.
</li><li>Maintain oversight of retained samples, batch documentation and traceability in line with site policies.
</li><li>Coach production teams on good manufacturing practice and promote continuous improvement.
</li><li>Participate in internal audits, validations and quality risk assessments as required.
</li></ul> 
Experience, Education and Skills
 
- Pharm- D, MSc in Chemistry Sciences is required for this role.
 
<ul><li>2-3 years of experience in pharmaceutical manufacturing, quality assurance or production operations.
</li><li>Practical understanding of Good Manufacturing Practice (GMP) and quality systems.
</li><li>Good written and verbal communication skills in English.
</li><li>Proficiency with Microsoft Office tools.
</li><li>Willingness to work on-site and to be present for production shifts as required.
</li><li>Experience in investigations, root cause analysis and CAPA implementation.
</li><li>Familiarity with quality management systems, data integrity and batch release processes.
</li><li>Exposure to internal auditing, validation activities or regulatory inspections.
</li><li>Training or certification in Lean, Six Sigma, or yellow/green belt would be a plus.
</li><li>Strong analytical skills with attention to detail and practical problem solving. 
</li></ul></div> 
Location and Working Pattern
 
This role is based in Pakistan and is on-site at a manufacturing facility. Shift work may be required to cover production hours.
 
 
How to apply
 
If you want to grow your quality career and make a real impact for patients, we want to hear from you. Please submit your application and tell us how your experience fits this role. We welcome applicants from all backgrounds and promote an inclusive workplace where everyone can contribute and grow.
Why GSK?
 
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
Contact information:
 
You may apply for this position online by selecting the Apply now button.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</div>

OQ Officer

SKONZS

SQA EngineerWe are looking for an SQA Engineer who can take full ownership of quality across our product ecosystem. If you know how to break things intelligently, automate where it matters, and build reliable release pipelines, you will fit right in.Responsibilities<ul><li>Design and execute test plans, test cases, and test scenarios for web and backend services.</li><li>Perform functional testing, regression testing, integration testing, and API testing.</li><li>Develop and maintain automated test suites (Python or JavaScript preferred).</li><li>Work closely with engineering and product teams to identify gaps and ensure timely issue resolution.</li><li>Identify, log, and track defects with clarity and ownership.</li><li>Create clear, detailed bug reports and track them through closure.</li><li>Validate performance, reliability, and edge-case scenarios before each deployment</li><li>Contribute to CI/CD quality gates and release readiness processes</li><li>Run performance and load testing to ensure scalability under real traffic conditions</li></ul>Requirements<ul><li>Bachelor&rsquo;s degree in Computer Science, Software Engineering, or related field</li><li>Solid understanding of QA methodologies, SDLC, and STLC</li><li>Hands-on experience in manual testing and basic automation</li><li>Good understanding of REST APIs, Postman, and SQL queries</li><li>Strong analytical skills and attention to detail</li><li>Ability to work in a fast-paced, product-focused environment</li></ul>Nice to Have<ul><li>Exposure to load testing and performance tools</li><li>Experience with tools like Selenium, Playwright, Cypress, or similar</li><li>Experience with Git, CI/CD tools, or containerized environments</li></ul>How to apply Email your resume at hello@skonzs.io under the subject &quot;SQA Engineer&quot;.Location: Karachi (Onsite) Employment Type: Full-timeJob Type: Full-timeApplication Question(s):<ul><li>What is your current Salary?</li><li>Salary Expectation: </li></ul>Education:<ul><li>Bachelor's (Preferred)</li></ul>Experience:<ul><li>SQA Engineer: 2 years (Preferred)</li></ul>Work Location: In person

Software Quality Assurance / SQA

Explore 1134+ Quality assurance specialist in Karachi this December. Find roles across top companies and apply now to boost your career.

1134 quality assurance specialist jobs IN Karachi

Clinical Trials Quality Assurance Associate (Night)

Clinical Trials Quality Assurance Associate (Night)

Consultant QA, QC

Software Quality Assurance Engineer

Mid Level Software Engineer – Quality Assurance

OQ Officer

Software Quality Assurance / SQA