quality assurance associate (clinical trial data)(evening shift)

assistant manager / manager quality assurance

assistant/manager-quality & regulatory compliance

junior analyst - associate Jobs in Karachi

junior analyst - associate

lab analyst

quality assurance associate (clinical trial data)(evening shift) Jobs in Karachi

assistant manager / manager quality assurance Jobs in Karachi

assistant/manager-quality & regulatory compliance Jobs in Karachi

quality associate

NielsenIQ

<div>Company Description 
Join GfK and help us shape tomorrow. As an NIQ company, we are the world's leading consumer intelligence firm, delivering the Full View&trade; on consumer behavior. We work to enable manufacturers and retailers better understand what consumers really want. Our name has inspired trust for over 89 years because we take pride in discovering new pathways to sustainable growth for our clients, our people, and our planet. 
Job Description 
<ul><li>
Execute low to medium complexity quality control tasks under supervision.</li><li>
Ensure accurate setting of QC Ratings as a quality benchmark and foundation for further analysis.</li><li>
Maintain compliance with global quality standards as defined by the MI OPS framework.</li><li>
Identify and report quality issues, inconsistencies, or process gaps.</li><li>
Collaborate with cross-functional teams to support continuous improvement initiatives.</li></ul> 

Qualifications 
<ul><li>
Ability to complete assigned tasks on time with high accuracy and attention to detail.</li><li>
Strong technical skills to perform quality checks effectively, including deeper knowledge of tools and systems used.</li><li>
Solid written and verbal communication skills for clear documentation and collaboration.</li><li>
Good analytical and problem-solving abilities to assess data and identify root causes.</li><li>
Sound judgment in handling ambiguous or complex situations.</li><li>
Product knowledge in a limited set of Product Groups.</li><li>
Proficiency in MS Office (Excel, Word, Outlook, etc.).</li><li>
A collaborative mindset and strong interpersonal skills to work effectively in a team environment.</li><li>
Should have a bachelors degree.</li></ul> 

Additional Information<div></div> 
Our Benefits<ul><li>
Flexible working environment</li><li>
Volunteer time off</li><li>
LinkedIn Learning</li><li>
Employee-Assistance-Program (EAP)</li></ul>
NIQ may utilize artificial intelligence (AI) tools at various stages of the recruitment process, including r&eacute;sum&eacute; screening, candidate assessments, interview scheduling, job matching, communication support, and certain administrative tasks that help streamline workflows. These tools are intended to improve efficiency and support fair and consistent evaluation based on job-related criteria. All use of AI is governed by NIQ&rsquo;s principles of fairness, transparency, human oversight, and inclusion. Final hiring decisions are made exclusively by humans. NIQ regularly reviews its AI tools to help mitigate bias and ensure compliance with applicable laws and regulations. If you have questions, require accommodations, or wish to request human review were permitted by law, please contact your local HR representative. For more information, please visit NIQ&rsquo;s AI Safety Policies and Guiding Principles: https://www.nielseniq.com/global/en/ai-safety-policies.

About NIQ
NIQ is the world&rsquo;s leading consumer intelligence company, delivering the most complete understanding of consumer buying behavior and revealing new pathways to growth. In 2023, NIQ combined with GfK, bringing together the two industry leaders with unparalleled global reach. With a holistic retail read and the most comprehensive consumer insights&mdash;delivered with advanced analytics through state-of-the-art platforms&mdash;NIQ delivers the Full View&trade;. NIQ is an Advent International portfolio company with operations in 100+ markets, covering more than 90% of the world&rsquo;s population.
For more information, visit NIQ.com
Want to keep up with our latest updates?
Follow us on: LinkedIn | Instagram | Twitter | Facebook

Our commitment to Diversity, Equity, and Inclusion
At NIQ, we are steadfast in our commitment to fostering an inclusive workplace that mirrors the rich diversity of the communities and markets we serve. We believe that embracing a wide range of perspectives drives innovation and excellence. All employment decisions at NIQ are made without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital status, veteran status, or any other characteristic protected by applicable laws. We invite individuals who share our dedication to inclusivity and equity to join us in making a meaningful impact. To learn more about our ongoing efforts in diversity and inclusion, please visit the https://nielseniq.com/global/en/news-center/diversity-inclusion</div>

Quality Associate

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 Operations, 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 in accordance with 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>
Provides 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, 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>
Fresh MBBS with keen interest in Clinical Research are strongly encouraged to apply, PharmD graduates will also be prefered.</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.</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 with respect to 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 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:
03 positions (Evening shift) 
Full-time 
On-site job 
 
Work Schedule Timings: 
Monday to Friday 
7 PM to 3 AM (transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
xaiHnpkG7W</div>

Quality Assurance Associate (Clinical Trial Data)(Evening Shift)

<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 Operations, 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 in accordance with 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>
 Provides 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, 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>
 Fresh MBBS with keen interest in Clinical Research are strongly encouraged to apply, PharmD graduates will also be prefered
 </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
 </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 with respect to 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 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:
 
 
 
 03 positions
 
 (Evening shift)
 
 
 
 Full-time
 
 
 On-site job
 
 
 
 Work Schedule Timings:
 
 
 
 Monday to Friday
 
 
 7 PM to 3 AM (transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
 
 
 Powered by JazzHR
 
 
 xaiHnpkG7W
</div>

<div>
 
 Site Name:
 
 Pakistan - Sindh - Karachi
 
 
 
 Posted Date:
 
 Mar 3 2026
 
 
 
 Job Purpose
 
 
 
 You will support the Data Integrity team to ensure accurate, reliable and compliant data across manufacturing and quality systems. You will work closely with quality, production and MSAT teams to perform Data Process Maps and Data Vulnerability Assessments of the Manufacturing, Packaging and QC Testing Processes. We value curiosity, attention to detail, teamwork and a desire to learn. This role offers hands-on experience, clear learning pathways, and a chance to contribute to work that supports better health outcomes by uniting science, technology and talent.
 
 
 
 Responsibilities
 
 
 
 
 <ul>
 <li>
 Support in performing the data process maps and data vulnerability assessments of Manufacturing, Packaging and QC Testing Processes.
 </li>
 <li>
 Participate in validation activities and support implementation of data integrity improvements.
 </li>
 <li>
 Record data vulnerabilities identified in data process maps clearly and escalate risks to the line manager or data integrity lead.
 </li>
 <li>
 Work with colleagues to close corrective and preventive actions and verify effectiveness to mitigate the identified vulnerabilities during data process maps.
 </li>
 <li>
 Support training activities to promote consistent data integrity and quality behaviors.
 </li>
 <li>
 Contribute to continuous improvement ideas for safer, leaner and more reliable processes.
 
 
 
 </li>
 </ul>
 
 Experience, Education And Skills
 
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Pharmacy, Pharm-D, Chemistry, Life Sciences or similar field.
 </li>
 <li>
 0&ndash;1 year relevant experience; fresh graduates with internship experience are welcome.
 </li>
 <li>
 Good understanding of good manufacturing practices and good documentation practices.
 </li>
 <li>
 Basic computer skills and proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook).
 </li>
 <li>
 Strong attention to detail and the ability to follow procedures consistently.
 </li>
 <li>
 Good written and verbal communication skills and ability to work in a team.
 </li>
 <li>
 Demonstrated continuous learning mindset and willingness to take on new responsibilities.
 
 
 
 </li>
 </ul>
 
 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>

Project Trainee Data Integrity

The Hive

Duties &amp; Responsibilities:<ul><li>Act as the first point of contact for all members, guests and visitors</li><li>Greet, register, and check in guests in a professional and courteous manner</li><li>Ensure adherence to visitor protocols and access controls</li><li>Maintain a welcoming and brand-aligned front desk presence at all times</li><li>Schedule, conduct, and manage facility tours for walk-ins and scheduled prospects</li><li>Record all walk-ins, tours, and interactions accurately in the CRM</li><li>Share approved, accurate information on memberships, services and pricing</li><li>Follow up with prospects as per defined follow-up timelines</li><li>Support conversion activities within assigned authority limits</li><li>Manage ancillary sales, including: Day passes, Meeting rooms, Boardrooms, Shared workspace offerings</li><li>Ensure correct pricing, invoicing, and system entries for all transactions</li><li>Escalate exceptions or discount requests for approval where required</li><li>Support the Community Associate in onboarding new members</li><li>Ensure onboarding documentation and system entries are complete and accurate</li><li>Assist in building rapport and addressing member needs during early engagement</li><li>Flag potential retention risks to the Community Associate or City Manager</li><li>Maintain accurate and up-to-date records in the CRM and internal trackers</li><li>Log all client interactions (calls, emails, messages) in the system</li><li>Update daily, weekly and monthly reports as required</li><li>Ensure data accuracy, completeness and visibility at all times</li><li>Handle inbound and outbound communications across voice and non-voice channels</li><li>Maintain professional call quality standards and response SLAs</li><li>Use approved communication templates and escalation protocols</li><li>Support planning, coordination, and execution of events with the Community Associate</li><li>Assist with guest management, registrations and on-ground coordination during events</li><li>Adhere to all SOPs, brand guidelines and code of conduct</li><li>Maintain confidentiality of member and company information</li><li>Escalate operational, service or compliance issues promptly</li><li>Perform additional duties aligned with role requirements as assigned by management</li><li>The Community Officer&rsquo;s performance will be evaluated based on: Guest &amp; member experience standards, Lead handling &amp; follow-up discipline, Data accuracy &amp; CRM compliance, Ancillary sales support, Communication quality &amp; professionalism, Adherence to SOPs &amp; reporting timelines</li></ul>Requirements:<ul><li>Proven experience as concierge; experience in customer service or relevant role is an advantage</li><li>Proficiency in English; multilingual is strongly preferred</li><li>Excellent communication skills</li><li>Polite and confident with a great deal of patience</li><li>Ability in multitasking and time-management</li><li>Aptitude in resolving issues with a customer-focused orientation</li><li>Degree in hotel management or relevant field will be a plus</li></ul>Job Type: Full-timeWork Location: In person

Community Officer

Ibex

We are seeking a proactive and customer-focused Global Customer Experience Associate to support our international clients. In this role, you will handle customer inquiries via phone, email, or chat, resolve issues efficiently, and deliver a high-quality service experience while maintaining company standards.Key Responsibilities:<ul><li>Respond to customer inquiries in a timely and professional manner</li><li>Resolve complaints and provide accurate information</li><li>Maintain detailed records of customer interactions</li><li>Meet performance and quality targets</li><li>Collaborate with internal teams to ensure customer satisfaction</li></ul>Requirements:<ul><li>Excellent English communication skills (spoken and written)</li><li>Strong problem-solving and interpersonal abilities</li><li>Basic computer proficiency</li><li>Ability to work in a fast-paced environment and night shifts</li></ul>Job Types: Full-time, Contract, Fresher Contract length: 6 monthsPay: Rs65,000.00 - Rs115,000.00 per monthWork Location: In person

Global Customer Experience Associate

Explore 609+ Quality associate in Karachi this March. Find roles across top companies and apply now to boost your career.

609 quality associate jobs In Karachi

Quality Associate

Quality Associate

Quality Assurance Associate (Clinical Trial Data)(Evening Shift)

Quality Assurance Associate (Clinical Trial Data)(Evening Shift)

Project Trainee Data Integrity

Community Officer

Global Customer Experience Associate