hr specialist

billing specialist

senior technical business analyst Jobs in Karachi

senior technical business analyst

academic qa executive (female) Jobs in Karachi

academic qa executive (female)

am / qc lab engineer for pharma sector Jobs in Karachi

am / qc lab engineer for pharma sector

quality assurance specialist

NCRI PAKISTAN PVT. LTD.

NCRi Solutions is seeking a versatile and highly experienced Specialist - Quality Assurance Engineer to join the Group Digital &amp; Technology team at AGI. In this role, you will act as a &quot;QA Floater,&quot; providing critical support across multiple platforms with a heavy focus on Mobile and Web applications. You will be the champion of a &quot;quality-first&quot; mindset, designing and executing test strategies that ensure our software solutions meet the highest standards of reliability and customer experience.Responsibilities:<ul><li>Align QA strategies with business objectives, product roadmaps, and customer expectations.</li><li>Ensure scalable and consistent testing practices across all mobile and web projects.</li><li>Promote Agile/Scrum best practices and a culture of continuous improvement.</li><li>End-to-End Testing: Design, develop, and execute comprehensive manual and automated test cases.</li><li>Test Automation: Build and maintain robust automation frameworks for mobile (iOS/Android) and web platforms.</li><li>API &amp; Integration: Perform rigorous API testing (REST/SOAP) and validate database integrity using SQL.</li><li>Performance &amp; Security: Conduct performance, load, and regression testing to ensure system stability.</li><li>Defect Management: Identify, document, and track software defects, collaborating closely with developers for timely resolution.</li><li>CI/CD Integration: Integrate automated tests into CI/CD pipelines to facilitate rapid, high-quality releases.</li></ul>Key requirements:<ul><li>Minimum of 7+ years in Quality Assurance.</li><li>At least 5 years of hands-on experience specifically in Mobile and Web QA activities.</li><li>Proven experience working within Agile/Scrum frameworks in a large corporate environment.</li><li>Bachelor&rsquo;s degree in Computer Science, IT, or a related Engineering subject.</li></ul>Preferred<ul><li>ISTQB Foundation or Advanced certification.</li><li>Microsoft Azure Fundamentals or Developer Associate certification.</li></ul>Technical Skill Set<ul><li>Proficiency in Selenium (Java), Appium, Playwright, or Cypress.</li><li>Testing Frameworks: TestNG, Rest Assured, and Postman for API testing.</li><li>Familiarity with JMeter or Gatling.</li><li>Strong understanding of Git and CI/CD processes.</li><li>Ability to write and execute complex SQL queries.</li><li>Maintain a leakage rate of less than 5%.</li><li>Achieve 95&ndash;100% functional coverage and 70&ndash;90% automation coverage.</li><li>100% completion of committed test cases per sprint.</li></ul>Job Type: Full-timeWork Location: In person

Specialist - Quality Assurance Engineer

United King

United King Foods is hiring a Quality Assurance Officer for our food manufacturing facilities in Karachi. This role is ideal for Food Technologist candidate with experience in FMCG, Food Production, Quality Assurance (QA), and Quality Control (QC) who are confident working in a factory environment. Male preferred due to shift timingsKey Responsibilities<ul><li>Conduct quality inspection of raw materials, packaging, and finished goods</li><li>Perform in-process quality checks on the production floor</li><li>Ensure compliance with GMP, food safety, hygiene, and regulatory standards</li><li>Verify labeling accuracy including shelf life, weight, batch coding, and allergen information</li><li>Use lab testing equipment and measuring tools for quality verification</li><li>Maintain quality documentation for audits and compliance</li><li>Perform Root Cause Analysis (RCA) and implement CAPA for non-conformities</li><li>Coordinate with Production, Supply Chain, and Procurement regarding quality issues</li><li>Support internal audits and retail quality checks when required</li><li>Preferably have hands-on experience in container loading operations</li></ul>Requirements<ul><li>Bachelor&rsquo;s degree in Food Sciences</li><li>2&ndash;3 years of experience in Quality Control / Quality Assurance in FMCG or Food Industry</li><li>Strong knowledge of GMP, HACCP, food safety standards, and documentation</li><li>Ability to work independently in a fast-paced manufacturing environment</li><li>Willingness to work rotational shifts</li><li>Karachi-based candidates preferred</li></ul>Why Join Us?<ul><li>Established FMCG brand</li><li>Growth opportunities in manufacturing quality operations</li><li>Structured and performance-driven environment</li></ul>Location: Shafiq More Sweet Factory - KarimabadNote: This is a factory-based role requiring regular presence on the production floor.Job Type: Full-timePay: Rs50,000.00 - Rs60,000.00 per monthApplication Question(s):<ul><li>What is your current salary?</li><li>What is your expected salary?</li><li>What is your notice period?</li><li>Are you able to do rotational shifts?</li><li>Do you have hands-on experience in container loading operations?</li><li>For which location are you interested?</li></ul>1) Karimabad 2) Shafiq MoreWork Location: In person

Senior Officer/ Officer - Quality Assurance

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 (06 PM to 02 AM) 
(transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
AjYqzsoJFy</div>

Clinical Trials Quality Assurance Associate (Night)

<div>
 
 Site Name:
 
 Karachi West Wharf, Karachi Korangi
 
 
 
 Posted Date:
 
 Apr 9 2026
 
 
 
 Join the GSK Quality Science Graduate Programme &ndash; Pakistan, 2026: Help us get ahead of disease together
 
 
 
 
 Education required:
 
 BSc/MSc degree in Pharmacy, Microbiology, Chemistry or a related field of study, OR Pharm D. Graduation by Summer 2026
 
 
 
 Language requirement:
 
 Written and spoken fluency in English
 
 
 
 Other requirements:
 
 
 
 
 <ul>
 <li>
 Willingness to be geographically mobile (domestic) throughout rotations
 </li>
 <li>
 Candidates must have their degrees completed by August 2026 to be considered for this position
 
 
 
 </li>
 </ul>
 
 Location:
 
 Karachi, Pakistan
 
 
 
 Start date:
 
 August/September 2026
 
 
 
 Application deadline:
 
 We recommend you apply as soon as possible. This vacancy will close when we have received enough applications, so please apply as soon as you can so your application can be considered.
 
 
 
 Assessment Centre Date:
 
 May-June 2026
 
 
 
 Are you a talented and driven student or graduate eager to make an impact on billions of lives? Apply for the Quality Science programme at GSK today!
 
 
 
 The GSK Graduate Programme offers a unique opportunity to join our Global Supply Chain and play a key role in delivering life-saving medicines and vaccines to people in over 90% of the world.
 
 
 At GSK, we are on an exciting journey to establish a world-class global supply chain that will support the delivery of our new product portfolio and pipeline. Within the Global Supply Chain business (GSC), our dedicated teams are responsible for manufacturing and distributing medicines and vaccines worldwide. They oversee every stage of production, from ensuring the creation of high-quality products at our manufacturing sites to developing effective supply forecasting and managing regulatory inspections&mdash;all powered by digital, data, and analytics.
 
 
 We are seeking highly motivated graduates who are eager to grow into future engineering, operational, and technical roles within GSC. These positions involve working at our manufacturing sites to ensure the implementation of the latest, safe, efficient, and reliable processes and equipment. This programme presents an opportunity for you to cultivate your skills in an industry that is undergoing radical changes in the way it develops and manufactures products.
 
 
 
 Ahead together with tailored training and career development
 
 
 
 Whilst on the graduate programme, you can expect the following benefits:
 
 
 
 <ul>
 <li>
 Challenging and supportive environment for your professional and personal growth
 </li>
 <li>
 Opportunities to network and enhance visibility with senior leaders who will mentor, coach, and support you with career planning
 </li>
 <li>
 Development of technical skills through valuable on-the-job experience
 </li>
 <li>
 Work in roles that are individually tailored according to your discipline, with the aim of meeting your aspirations, strengths and ambitions (along with the needs of the business)
 </li>
 <li>
 Access to a generous personal development budget to accelerate learning and professional growth
 </li>
 <li>
 Kaizens &ndash; short-term breadth projects that offer potential international exposure
 
 
 
 </li>
 </ul>
 
 What will you do?
 
 
 
 
 <ul>
 <li>
 Discover how manufacturing, the quality function, technical services and supply chain work together
 </li>
 <li>
 Build your knowledge of our medicines and vaccines and learn about the challenges of working in a highly regulated and controlled environment
 </li>
 <li>
 Spend time in a quality testing laboratory at one of our Manufacturing sites - developing skills to perform analysis while gaining hands on experience using state-of-the art platforms and capabilities
 </li>
 <li>
 Gain an understanding about quality control - how analytical testing ensures the quality of our products, learn about the introduction of new technologies and analytical methods
 </li>
 <li>
 Quality gives an end-to-end understanding of the pharmaceutical products from raw materials to finished products, including sterility and environmental testing
 </li>
 <li>
 Develop business, process and test method understanding
 
 
 
 </li>
 </ul>
 
 What are we looking for?
 
 
 
 
 <ul>
 <li>
 Technical aptitude, a passion for quality, and a keen interest in pharmaceutical manufacturing
 </li>
 <li>
 A mindset focused on continuous improvement and growth, along with strong interpersonal skills and a positive approach
 </li>
 <li>
 The ability to listen, learn, and a genuine desire to make a meaningful impact on people&rsquo;s lives through high-quality work
 </li>
 <li>
 Excellent communication and problem-solving skills, coupled with a collaborative approach to teamwork
 </li>
 <li>
 Self-motivation, proactiveness, and a strong eagerness for development and learning
 </li>
 <li>
 Analytical, organized, and process-driven, with exceptional attention to detail
 </li>
 <li>
 High adaptability and flexibility, with the ability to perform effectively under pressure and embrace change
 
 
 
 </li>
 </ul>
 This programme is ideal for highly motivated individuals who are eager to embark on their careers in a complex manufacturing environment. Candidates should naturally embody GSK culture and demonstrate the potential to become outstanding subject matter experts.
 
 
 
 What do we offer you?
 
 
 
 
 <ul>
 <li>
 On-the-job experience
 </li>
 <li>
 Formal and informal technical and soft skills training and development, delivered through a mixture of coaching and mentoring by senior leaders, your manager, your peers, and a mix of virtual &amp; in person courses
 </li>
 <li>
 A competitive salary
 </li>
 <li>
 An annual bonus based on company performance
 </li>
 <li>
 Relocation support (subject to eligibility)
 </li>
 <li>
 Employee recognition programs, which reward exceptional achievements
 </li>
 <li>
 Well-being programs to help you be healthier, inspired and energized both at work and at home
 </li>
 <li>
 Access to healthcare plans and options
 </li>
 <li>
 Generous time off with pay, in addition to end of year company-wide shutdown
 </li>
 <li>
 2 volunteering days per year, called &ldquo;Together Days&rdquo;
 
 
 
 </li>
 </ul>
 
 Let&rsquo;s do this!
 
 
 
 You&rsquo;ll find hints, tips and guidance on our recruitment process on our website
 
 
 Learn more about the application process gsk.to/ECprocess
 
 
 Once you've submitted your online application form, you'll need to complete two online assessments prior to the assessment center stage and as part of this, you'll be asked about your motivation for the role: We&rsquo;d like to hear about why you applied to this role and your motivation for the business area you&rsquo;ve applied to. You will be asked a 2nd question on what strengths, skills or interests you have that will enable you to be successful in this role.  Please be as targeted as you can!
 
 
 
 
 Top tip: Make sure you save this job description for reference throughout the process, it will really help you prepare for the different stages in your application.
 
 
 You can learn more about GSK and our careers here https://www.gsk.com/en-gb/careers/
 
 
 Our Graduate Programmes are designed to accelerate the development of graduates who don&rsquo;t have significant previous professional work experience in the area to which they are applying. Of course, many graduates who join the programme have worked while studying or after graduation. If you&rsquo;ve already developed substantial experience working in a professional role in your sector, while you would be able to apply for this programme, you may also want to look at direct entry roles in our businesses, as these may be the best way to build on your existing skills and expertise and develop a career at GSK.
 
 
 
 Apply now!
 
 
 
 
 Need help with your application?
 
 
 
 
 Please email us at
 
 EMEA.earlycareers@gsk.com
 
 and let us know how we can help you.
 
 
 
 #GraduateProgramme
 
 
 #GPEMEA2026
 
 
 #GPPakistan2026
 
 
 #ManufacturingSupplyChainGP
 
 
 #EngineeringGP
 
 
 #ManufacturingScienceGP
 
 
 #EarlyCareers
 
 
 We are seeking highly motivated graduates who are eager to grow into future QA, QC and technical specialist roles within GSC. These positions will place you on site and in laboratories where you will support analytical testing and method validation, batch record review and release, deviation investigations and CAPA, regulatory readiness and supplier quality activities. The programme offers hands‑on experience with modern analytical platforms and quality systems, and the chance to contribute to continuous improvement, quality by design and the digital transformation of our quality practices &mdash; all while developing the technical and professional skills to become a subject matter expert.
 
 
 
 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>

Quality Science Graduate Programme, Pakistan, 2026

THERMOLINE PVT LTD

<ul><li>Develop, implement, and maintain quality control systems and procedures</li><li>Monitor production processes to ensure compliance with quality standards</li><li>Conduct inspections, audits, and tests on materials and finished products</li><li>Identify defects or issues and implement corrective and preventive actions</li><li>Ensure compliance with industry standards and regulations</li><li>Analyze quality data and generate reports for management</li><li>Lead and train quality control staff and inspectors</li><li>Collaborate with production, engineering, and supply chain teams</li><li>Handle customer complaints and ensure timely resolution</li><li>Drive continuous improvement initiatives to enhance product quality</li></ul>Work Environment<ul><li>Typically works in manufacturing, production, or industrial settings</li><li>May require standing, inspecting materials, and visiting production floors</li></ul>Key Performance Indicators (KPIs)<ul><li>Product defect rate</li><li>Customer complaint resolution time</li><li>Compliance audit scores</li><li>Process improvement outcomes</li><li>Cost of poor quality (COPQ)</li></ul>Job Type: Full-timePay: Rs50,000.00 - Rs100,000.00 per monthWork Location: In person

QUALITY CONTROL MANAGER FOR INJECTION MOULDING MACHINES

Walkeaze

.Conducting fragrance quality testing (longevity, scent accuracy, projection, and batch consistency).<ul><li>Inspecting fragrance packaging, bottle finishing, labeling accuracy, and barcode compliance.</li><li>Supervising skincare testing processes including patch testing coordination and allergen review.</li><li>Ensuring packaging integrity, labeling compliance, and regulatory adherence for skincare products.</li><li>Managing product development processes including formula coordination and packaging design.</li><li>Collaborating with suppliers, production teams, and QA departments.</li><li>Documenting R&amp;D findings and reporting progress to management.</li><li>Maintaining and updating Power BI dashboards for product performance, sales trends, and development tracking.</li><li>Conducting market research, competitor analysis, and outlet visits.</li></ul>1-2 years of experience, preferably within fragrance, skincare and cosmetics Bachelor&rsquo;s Degree Share Cv at hr@walkeaze.comWork Location: In person

Perfume Specialist

Paksa IT soloutions (Pvt.) Limited

What you&rsquo;ll do:<ul><li>Test web, mobile, and backend systems (functional, regression, integration)</li><li>Perform API testing using Postman/Swagger</li><li>Build and maintain automation (Selenium, Cypress, Playwright)</li><li>Integrate tests into CI/CD pipelines</li><li>Validate AI features (chatbots, recommendations, predictions)</li><li>Run performance tests (JMeter/k6) and basic security checks</li><li>Log bugs (Jira/ClickUp) and maintain QA documentation</li></ul>Requirements:<ul><li>Bachelor&rsquo;s in CS/SE or related</li><li>Experience in manual + automation testing</li><li>Strong API testing skills (Postman &ndash; mandatory)</li><li>Python or JavaScript</li><li>Experience with Selenium/Cypress/Playwright</li><li>Familiarity with PyTest, Jest, or Mocha</li></ul>Application Question(s):<ul><li>Do you have hands-on API testing experience using Postman? (Yes/No)</li><li>Which automation tools have you used? (Selenium / Cypress / Playwright / Other)</li><li>Do you have experience with CI/CD integration? (Yes/No)</li><li>Which language are you comfortable with? (Python / JavaScript)</li><li>Years of QA experience?</li><li>Any experience testing AI systems/chatbots? (Yes/No)</li><li>Current salary &amp; expected salary (PKR)?</li><li>Notice period?</li></ul>Work Location: In person

Quality Assurance Engineer – Software & AI Systems

Explore 558+ Quality assurance specialist in Karachi this April. Find roles across top companies and apply now to boost your career.