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quality assurance manager Jobs in Karachi Pakistan

quality assurance manager

sqa engineer

assistant manager qa-qms Jobs in Karachi Pakistan

assistant manager qa-qms

quality control manager

L'Oréal

<div>
 <strong>
  Overview
  <br/>
  <br/>
 </strong>
 The Quality Assurance Manager assures quality products and processes by establishing and enforcing quality standards; testing materials and product that assures proper adherence to company requirements and global standards.
 <br/>
 <br/>
 <strong>
  Key Job Accountabilities
  <br/>
  <br/>
 </strong>
 Strategic Contribution:
 <br/>
 <br/>
 <ul>
  <li>
   Drives the Quality Assurance agenda to support the manufacturing strategy for providing high quality products to customers.
  </li>
  <li>
   Functional Policies and Controls:
  </li>
  <li>
   Monitors the effectiveness of the Quality function establishing Quality Assurance and control programs, policies and procedures which ensure product integrity and compliance with group standards and specifications.
  </li>
  <li>
   Set up and maintain quality controls and documentation procedures.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Analytics
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Responsible for product and process quality reports by collecting, analyzing, and summarizing information and trends.
  </li>
  <li>
   Preparing and analyzing reports on design, pre-production, and production to check on the quality status of the product at all stages of production and inform the production team.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Quality Assurance
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Ensuring all Finished Goods, Raw Material and Packaging Material lab testing is done as per L&rsquo;Oreal methods and specifications in the following labs:
  </li>
  <li>
   Testing of cosmetics related products in Micro-biological lab
  </li>
  <li>
   Packaging material parameters testing in Physical lab
  </li>
  <li>
   Raw material testing - Chemical Lab
  </li>
  <li>
   Bulk testing or To be filled products testing in In-process testing lab
  </li>
  <li>
   Ensure the timely and accurate evaluations of raw materials, packaging components, manufactured batches, in process materials and finished products.
  </li>
  <li>
   Ensures production record documentation is accurate.
  </li>
  <li>
   Creating batch making records to guarantee quality from stage one.
  </li>
  <li>
   Recommends the acceptance or blocking of deliveries or production in accordance with L&rsquo;Or&eacute;al specifications.
  </li>
  <li>
   Drive efficiency and implement quality as part of Operational excellence pillar.
  </li>
  <li>
   Works with production manager to understand the root causes of the problems in the operations.
  </li>
  <li>
   Coordinate with Unit Production to lead and monitor RTFT (Right the first time) for all local manufacturing.
  </li>
  <li>
   Formalizing methods of manufacturing for all new Fla&rsquo;s (Formulas) to guarantee quality from stage one and getting it validated from Zone Quality team for processing.
  </li>
  <li>
   Lead raw material diversification/localization process in coordination with local purchasing team and zone quality team.
   <br/>
   <br/>
  </li>
 </ul>
 Quality Audits
 <br/>
 <br/>
 <ul>
  <li>
   Responsible for leading all investigations or audits concerning product quality.
  </li>
  <li>
   Ensure supplier quality audits are conducted to gauge performance and share feedback for improvement.
  </li>
  <li>
   Ensure quarterly quality audits are happening of all critical processes and share feedback for improvement.
   <br/>
   <br/>
  </li>
 </ul>
 Continuous Improvement
 <br/>
 <br/>
 <ul>
  <li>
   Liaise with other managers and staff and provide training, tools and techniques to enable others to achieve quality standards.
  </li>
  <li>
   Implementing improvements to production processes that lead to overall increases in product quality.
  </li>
  <li>
   Look at ways to reduce waste and increase efficiency in production line.
  </li>
  <li>
   Measure performance and identify any areas of weakness, recommending and implementing improvements
  </li>
  <li>
   Utilizing extensive knowledge of the product's inner workings to diagnose problems.
  </li>
  <li>
   Continuing education on newly developing Quality Assurance techniques.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  People Development
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Supervises Quality engineers and Lab team in their day-to-day tasks. Provide recommendations to the Line Manager and Human Resources on hiring and promotions.
  </li>
  <li>
   Consistently promotes high standards through personal example and roll out through the team so that each member of the team understands the standards and behaviors expected of them.
  </li>
  <li>
   Setting individual objectives, conduct periodic performance reviews, providing feedback and appraisal to maximize subordinates and departmental performance.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  KEY STAKEHOLDERS
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Internal: Manufacturing, Supply Chain, Marketing, Commercial and other departments within L&rsquo;Or&eacute;al
  </li>
  <li>
   External: 3rd Party Manufacturing team, Suppliers, Auditors, Quality Assurance Institutes
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 Minimum Qualifications:
 <br/>
 <br/>
 <ul>
  <li>
   BSc Engineering (any discipline)
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Minimum Experience
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   6- years of experience in Quality Assurance in FMCG/Process industry
  </li>
  <li>
   At least 3 years in managing role
  </li>
  <li>
   Extensive knowledge of Quality Assurance/Quality Control systems and procedures, chemistry, biological sciences, statistics, managerial disciplines, Federal Regulations (cosmetic, drug, food).
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Behavioral Skills
  <br/>
  <br/>
 </strong>
 <strong>
  EXPERIENCE &amp; SKILLS
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Creative problem-solving skills and ability to thrive in an entrepreneurial environment are a must
  </li>
  <li>
   Dynamic &amp; Resilient and happy to do business at fast pace
  </li>
  <li>
   Able to manage team effectively
  </li>
  <li>
   Demonstrate a strong power of analytical reasoning that can drive the business forward
  </li>
  <li>
   Highly conscientious and diligent.
  </li>
  <li>
   Data analysis and statistical aptitude
  </li>
  <li>
   Ability to facilitate change
  </li>
  <li>
   Team Management
  </li>
  <li>
   Leadership Skills
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Competencies
  <br/>
  <br/>
 </strong>
 Technical Competencies
 <br/>
 <br/>
 <ul>
  <li>
   Hands-on knowledge of Inspection Equipment
  </li>
  <li>
   Thorough knowledge of Good Manufacturing Practices (GMP)
  </li>
  <li>
   Commitment to the quality function
  </li>
  <li>
   Ability to make effective and efficient use of financial resources to achieve objectives
  </li>
  <li>
   Knowledge of manufacturing and filling of bulk, and the operation of various types of manufacturing and packaging equipment
  </li>
 </ul>
</div>


Quality Assurance Manager

<div><div><b>OVERVIEW</b></div><div></div><div><br>
The Quality Assurance Manager assures quality products and processes by establishing and enforcing quality standards; testing materials and product that assures proper adherence to company requirements and global standards.</div><div></div><div><b><br>
KEY JOB ACCOUNTABILITIES</b></div><div>
Strategic Contribution:</div><div><ul><li>
Drives the Quality Assurance agenda to support the manufacturing strategy for providing high quality products to customers.</li><li>
Functional Policies and Controls:</li><li>
Monitors the effectiveness of the Quality function establishing Quality Assurance and control programs, policies and procedures which ensure product integrity and compliance with group standards and specifications.</li><li>
Set up and maintain quality controls and documentation procedures.</li></ul></div><div>
Analytics:</div><div><ul><li>
Responsible for product and process quality reports by collecting, analyzing, and summarizing information and trends.</li><li>
Preparing and analyzing reports on design, pre-production, and production to check on the quality status of the product at all stages of production and inform the production team.</li></ul></div><div>
Quality Assurance:</div><div><ul><li>
Ensuring all Finished Goods, Raw Material and Packaging Material lab testing is done as per L&rsquo;Oreal methods and specifications in the following labs:</li><li>
Testing of cosmetics related products in Micro-biological lab</li><li>
Packaging material parameters testing in Physical lab</li><li>
Raw material testing - Chemical Lab</li><li>
Bulk testing or To be filled products testing in In-process testing lab</li><li>
Ensure the timely and accurate evaluations of raw materials, packaging components, manufactured batches, in process materials and finished products.</li><li>
Ensures production record documentation is accurate.</li><li>
Creating batch making records to guarantee quality from stage one.</li><li>
Recommends the acceptance or blocking of deliveries or production in accordance with L&rsquo;Or&eacute;al specifications.</li><li>
Drive efficiency and implement quality as part of Operational excellence pillar.</li><li>
Works with production manager to understand the root causes of the problems in the operations.</li><li>
Coordinate with Unit Production to lead and monitor RTFT (Right the first time) for all local manufacturing.</li><li>
Formalizing methods of manufacturing for all new Fla&rsquo;s (Formulas) to guarantee quality from stage one and getting it validated from Zone Quality team for processing.</li><li>
Lead raw material diversification/localization process in coordination with local purchasing team and zone quality team.</li></ul></div><div>
Quality Audits</div><div><ul><li>
Responsible for leading all investigations or audits concerning product quality.</li><li>
Ensure supplier quality audits are conducted to gauge performance and share feedback for improvement.</li><li>
Ensure quarterly quality audits are happening of all critical processes and share feedback for improvement.</li></ul></div><div>
Continuous Improvement</div><div><ul><li>
Liaise with other managers and staff and provide training, tools and techniques to enable others to achieve quality standards.</li><li>
Implementing improvements to production processes that lead to overall increases in product quality.</li><li>
Look at ways to reduce waste and increase efficiency in production line.</li><li>
Measure performance and identify any areas of weakness, recommending and implementing improvements</li><li>
Utilizing extensive knowledge of the product's inner workings to diagnose problems.</li><li>
Continuing education on newly developing Quality Assurance techniques.</li></ul></div><div>
People Development:</div><div><ul><li>
Supervises Quality engineers and Lab team in their day-to-day tasks. Provide recommendations to the Line Manager and Human Resources on hiring and promotions.</li><li>
Consistently promotes high standards through personal example and roll out through the team so that each member of the team understands the standards and behaviors expected of them.</li><li>
Setting individual objectives, conduct periodic performance reviews, providing feedback and appraisal to maximize subordinates and departmental performance.</li></ul></div><div></div><div><b><br>
KEY STAKEHOLDERS</b></div><div></div><div><br>
<ul><li>
Internal: Manufacturing, Supply Chain, Marketing, Commercial and other departments within L&rsquo;Or&eacute;al</li><li>
External: 3rd Party Manufacturing team, Suppliers, Auditors, Quality Assurance Institutes</li></ul></div><div></div><div><b><br>
QUALIFICATIONS</b></div><div></div><div><br>
Minimum Qualifications:</div><div><ul><li>
BSc Engineering (any discipline)</li></ul></div><div>
Minimum Experience:</div><div><ul><li>
6- years of experience in Quality Assurance in FMCG/Process industry</li><li>
At least 3 years in managing role</li><li>
Extensive knowledge of Quality Assurance/Quality Control systems and procedures, chemistry, biological sciences, statistics, managerial disciplines, Federal Regulations (cosmetic, drug, food).</li></ul></div><div></div><div><br>
 <b>EXPERIENCE &amp; SKILLS</b></div><div></div><div><br>
Behavioral Skills:</div><div><ul><li>
Creative problem-solving skills and ability to thrive in an entrepreneurial environment are a must</li><li>
Dynamic &amp; Resilient and happy to do business at fast pace</li><li>
Able to manage team effectively</li><li>
Demonstrate a strong power of analytical reasoning that can drive the business forward</li><li>
Highly conscientious and diligent.</li><li>
Data analysis and statistical aptitude</li><li>
Ability to facilitate change</li><li>
Team Management</li><li>
Leadership Skills</li></ul></div><div></div><div><b><br>
COMPETENCIES:</b></div><div>
Technical Competencies</div><div><ul><li>
Hands-on knowledge of Inspection Equipment</li><li>
Thorough knowledge of Good Manufacturing Practices (GMP)</li><li>
Commitment to the quality function</li><li>
Ability to make effective and efficient use of financial resources to achieve objectives</li><li>
Knowledge of manufacturing and filling of bulk, and the operation of various types of manufacturing and packaging equipment</li></ul></div></div>

ASF security foundation pvt.

<ul><li><b>Incoming Material Inspection:</b></li><li>Inspect raw materials (PET resin, color masterbatch, caps, preforms, etc.) for compliance with specifications.</li><li>Verify supplier certificates and maintain records.</li><li><b>In-Process Quality Control:</b></li><li>Conduct visual and dimensional inspection of bottles at various production stages (blow molding, filling, labeling, packing).</li><li>Check for defects such as short shots, black spots, bubbles, uneven thickness, or deformation.</li><li>Monitor machine parameters affecting bottle quality (temperature, pressure, blowing time).</li><li>Ensure operators follow standard operating procedures (SOPs).</li><li><b>Final Product Inspection:</b></li><li>Perform physical and functional tests such as:</li><li>Wall thickness &amp; weight check</li><li>Drop test</li><li>Top load test</li><li>Burst pressure test</li><li>Leakage test</li><li>Transparency and color check</li><li>Approve or reject finished lots based on quality test results.</li><li><b>Documentation and Reporting:</b></li><li>Maintain daily inspection reports and test records.</li><li>Prepare quality deviation reports and corrective action records.</li><li>Support ISO and customer audits by providing quality documentation.</li><li><b>Quality Improvement:</b></li><li>Identify recurring defects and assist in root cause analysis.</li><li>Coordinate with production and maintenance teams to implement corrective and preventive actions (CAPA).</li><li>Participate in continuous improvement programs (5S, Kaizen, etc.).</li></ul><p>Job Types: Full-time, Fresher</p><p>Pay: From Rs25,000.00 per month</p><p>Work Location: In person</p>

Quality Controller

<div><b>Site Name:</b> Pakistan - Sindh - Karachi<br>
<b>Posted Date:</b> Nov 7 2025<p><b><br>
Job Purpose
</b></p><p>The Site Regulatory Compliance Head at GSK is responsible for ensuring that all company operations, products, and processes comply with relevant regulatory requirements. The role involves developing, implementing, and managing regulatory compliance programs and procedures to ensure adherence to laws, regulations, and guidelines set by regulatory bodies. The Regulatory Compliance Manager will play a critical role in maintaining the company's reputation and protecting it from GMP and regulatory compliance risks. The role ensures the risks are identified, escalated and mitigation plans In-place. This position ensures that all critical Quality Regulatory Compliance activities at the site comply with applicable regulatory authority guidelines, QMS requirements, cGMP standards, and applicable local standard operating procedures.</p><p></p><p><b>
Education, Experience &amp; Skills</b></p><ul><li>
Science Graduate/Pharm D/ /Pharmacist</li><li>
Minimum 8 years of Experience in Quality Assurance, Regulatory Compliance, Quality Control, or a related field, including a position of significant leadership and decision-making authority within Quality or Regulatory functions.</li><li>
Strong knowledge of QMS, GMP and Regulatory requirements and guidelines</li></ul><p></p><p><b>
Key Responsibilities</b></p><ul><li>
Manage Quality Regulatory Compliance and systems on site by creating and executing regulatory compliance strategies and programs.</li><li>
Ensure to monitor changes in global and local regulatory environment/regulatory requirements and ensure GSK processes and products comply with applicable laws and regulations.</li><li>
Establish, review, and update site procedures to align with regulatory requirements.</li><li>
Accountable for timely communication, correspondence with Regulators, government officials for warrantors, queries, cases and any other correspondence in liaison with Site, Legal and Regulatory team.</li><li>
Responsible for attending meetings and hearings with government officials and regulators in liaison with Site Quality Head</li><li>
Proactive engagement with regulator, where possible e.g. DTL, PQCB to expediate the current ongoing regulatory queries</li><li>
Investigate and resolve compliance issues, including conducting root cause analysis and implementing corrective actions.</li><li>
Identify Internal and external risks, where applicable develop risk mitigation plan and monitor the implementation plan.</li><li>
Governance of regulatory KPIs and processes and identify and assess compliance risks to develop effective mitigation strategies.</li><li>
Engage and communicate effectively with internal stakeholders and senior management to ensure alignment on compliance matters.</li><li>
Ensure compliance of the site-specific regulatory process for Management of Regulatory authority letters notifications and statutory regulatory orders (SROs).</li><li>
Ensure the Inspection readiness at Site, escalates any issues which impacting inspection readiness to site senior management.</li><li>
Represent the site during regulatory inspections in coordination with site relevant team.</li><li>
Develop and maintain accurate records of site product registration details, regulatory submissions and correspondence with regulatory agencies.</li><li>
Ensures compliance with QMS Implementation on site to comply with the requirements of the QMS, company internal policies, Global SOPs, and all related regulatory guidelines.</li><li>
Engages with the site to promote a culture of awareness and understanding of regulatory compliance.</li><li>
Provide training to employees on regulatory compliance topics to enhance their understanding and adherence to applicable regulations.</li><li>
Ensure to maintain accurate and up-to-date records of regulatory activities, decisions, and communications.</li><li>
Ensure reporting of compliance risks and issues to Site Quality Head, Site Director and at governance forum i.e. Site Quality Council, Site Leadership Team meetings.</li><li>
Permanent member of Site Quality Council and Risk Management Council Board meetings.</li><li>
This role may require traveling to attend regulatory meetings, conferences, visits or inspections.</li></ul><p><b>
Job Purpose
</b></p><p></p><p>The Site Regulatory Compliance Head at GSK is responsible for ensuring that all company operations, products, and processes comply with relevant regulatory requirements. The role involves developing, implementing, and managing regulatory compliance programs and procedures to ensure adherence to laws, regulations, and guidelines set by regulatory bodies. The Regulatory Compliance Manager will play a critical role in maintaining the company's reputation and protecting it from GMP and regulatory compliance risks. The role ensures the risks are identified, escalated and mitigation plans In-place. This position ensures that all critical Quality Regulatory Compliance activities at the site comply with applicable regulatory authority guidelines, QMS requirements, cGMP standards, and applicable local standard operating procedures.</p><p></p><p><b>
Education, Experience &amp; Skills</b></p><ul><li><p>
Science Graduate/Pharm D/ /Pharmacist</p></li><li><p>
Minimum 8 years of Experience in Quality Assurance, Regulatory Compliance, Quality Control, or a related field, including a position of significant leadership and decision-making authority within Quality or Regulatory functions.</p></li><li><p>
Strong knowledge of QMS, GMP and Regulatory requirements and guidelines</p></li></ul><p></p><p><b>
Key Responsibilities</b></p><ul><li><p>
Manage Quality Regulatory Compliance and systems on site by creating and executing regulatory compliance strategies and programs.</p></li><li><p>
Ensure to monitor changes in global and local regulatory environment/regulatory requirements and ensure GSK processes and products comply with applicable laws and regulations.</p></li><li><p>
Establish, review, and update site procedures to align with regulatory requirements.</p></li><li><p>
Accountable for timely communication, correspondence with Regulators, government officials for warrantors, queries, cases and any other correspondence in liaison with Site, Legal and Regulatory team.</p></li><li><p>
Responsible for attending meetings and hearings with government officials and regulators in liaison with Site Quality Head</p></li><li><p>
Proactive engagement with regulator, where possible e.g. DTL, PQCB to expediate the current ongoing regulatory queries</p></li><li><p>
Investigate and resolve compliance issues, including conducting root cause analysis and implementing corrective actions.</p></li><li><p>
Identify Internal and external risks, where applicable develop risk mitigation plan and monitor the implementation plan.</p></li><li><p>
Governance of regulatory KPIs and processes and identify and assess compliance risks to develop effective mitigation strategies.</p></li><li><p>
Engage and communicate effectively with internal stakeholders and senior management to ensure alignment on compliance matters.</p></li><li><p>
Ensure compliance of the site-specific regulatory process for Management of Regulatory authority letters notifications and statutory regulatory orders (SROs).</p></li><li><p>
Ensure the Inspection readiness at Site, escalates any issues which impacting inspection readiness to site senior management.</p></li><li><p>
Represent the site during regulatory inspections in coordination with site relevant team.</p></li><li><p>
Develop and maintain accurate records of site product registration details, regulatory submissions and correspondence with regulatory agencies.</p></li><li><p>
Ensures compliance with QMS Implementation on site to comply with the requirements of the QMS, company internal policies, Global SOPs, and all related regulatory guidelines.</p></li><li><p>
Engages with the site to promote a culture of awareness and understanding of regulatory compliance.</p></li><li><p>
Provide training to employees on regulatory compliance topics to enhance their understanding and adherence to applicable regulations.</p></li><li><p>
Ensure to maintain accurate and up-to-date records of regulatory activities, decisions, and communications.</p></li><li><p>
Ensure reporting of compliance risks and issues to Site Quality Head, Site Director and at governance forum i.e. Site Quality Council, Site Leadership Team meetings.</p></li><li><p>
Permanent member of Site Quality Council and Risk Management Council Board meetings.</p></li><li><p>
This role may require traveling to attend regulatory meetings, conferences, visits or inspections.</p></li></ul><p></p><p><b>
Why GSK?</b><br>
<b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>
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.</p><p></p><p>
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.</p><p></p><p><b>
Contact information:</b><br>
You may apply for this position online by selecting the <b>Apply now</b> button.</p><p></p><p><b>
Important notice to Employment businesses/ Agencies</b></p><p>
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.</p></div>

Site Regulatory Compliance Head

Domino's

<p><b>Position: </b>Quality Assurance Associate Manager</p><p><b>Location: </b>Karachi</p><p><b>Role Overview:</b></p><p>To supervise and verify the Quality Assurance processes Dominos Stores as per DPI and Local Authorities Guidelines.<br/>Contribute to new business initiatives and projects and review and communicate the impact on Quality activities.</p><p><b>Key Responsibilities: </b></p><p>Expansion of testing and monitoring procedures of product quality of domino&rsquo;s pizza outlets.<br/>Creating, reviewing, and testing technical specifications documents and effective testing plans and test cases.<br/>Visiting Supplier&rsquo;s Facility for Continual Improvement on Food Safety Standards.<br/>Assist directly to Manager Quality during all the External Audits at all Regions as per DPI guidelines.<br/>Conduct Food safety and NSF guideline related trainings to all region for stores and Commissaries.</p><p><b>Required Skills and Competencies:</b></p><p>Knowledge of food safety standards.</p><p>Can conduct FS audits individually.</p><p>Have a sound knowledge of Food safety certifications.</p><p>Can travel alone.</p><p>Basic knowledge about third party audits at stores.</p><p>Responsible AND reliable in actions.</p><p><b>Experience: </b>4 to 5 Years</p><p><b>Qualification: </b>Bachelor's Degree in Food Science/Technology</p><p>Job Type: Full-time</p><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Work Location: In person</p>

Quality Assurance Associate Manager

Getz Pharma

<div>
 <p>
  <strong>
   Job Responsibilities:
  </strong>
 </p>
 <ul>
  <li>
   Initiate, assess, and manage change controls related to facilities, equipment, materials, processes, documents, and systems.
  </li>
  <li>
   Ensure proper risk assessment, impact analysis, and timely closure of change controls in compliance with ICH Q10 and WHO guidelines.
  </li>
  <li>
   Liaise with cross-functional departments to evaluate proposed changes and ensure adequate controls are in place.
  </li>
  <li>
   Oversee the logging, classification, and evaluation of deviations from approved processes and procedures.
  </li>
  <li>
   Lead cross-functional teams in conducting thorough
   <strong>
    root cause analysis (RCA)
   </strong>
   using scientific tools and methodologies.
  </li>
  <li>
   Ensure deviations are investigated, documented, and closed within defined timelines, with appropriate corrective and preventive actions.
  </li>
  <li>
   Ensure CAPAs are properly identified, implemented, tracked, and verified for effectiveness.
  </li>
  <li>
   Monitor trends in deviations, complaints, and audit findings to proactively identify areas for improvement.
  </li>
  <li>
   Facilitate CAPA boards or review meetings and maintain compliance with ICH Q10 principles of pharmaceutical quality systems.
  </li>
  <li>
   Apply systematic problem-solving tools such as
   <strong>
    5 Whys
   </strong>
   ,
   <strong>
    Ishikawa diagrams
   </strong>
   , etc. to identify true root causes.
  </li>
  <li>
   Train and mentor staff in effective RCA practices to strengthen the culture of quality and compliance.
  </li>
  <li>
   Conduct and review risk assessments (as per ICH Q9) to support decision-making for deviations, changes, and CAPAs.
  </li>
  <li>
   Implement risk mitigation strategies and monitor effectiveness over time.
  </li>
  <li>
   Support development and periodic review of risk management plans for critical processes and systems.
  </li>
  <li>
   Review completed batch manufacturing records (BMRs), quality control results, and associated documentation for compliance.
  </li>
  <li>
   Ensure that only conforming products are released, and that batch release meets applicable regulatory and internal quality standards.
  </li>
  <li>
   Ensure adherence to
   <strong>
    Good Documentation Practices (GDP)
   </strong>
   and review of SOPs, protocols, and reports.
  </li>
  <li>
   Support document control activities and ensure that controlled documents are maintained, revised, and distributed appropriately.
  </li>
  <li>
   Participate in data integrity initiatives and ensure records are attributable, legible, contemporaneous, original, and accurate (ALCOA+).
  </li>
  <li>
   Prepare and present QMS-related data and documents during internal audits and external inspections.
  </li>
  <li>
   Assist in timely closure of audit findings and implementation of sustainable improvements.
  </li>
  <li>
   Promote a culture of continuous improvement within the QA-QMS team.
  </li>
  <li>
   Identify trends and systemic issues using QMS metrics and propose preventive strategies.
  </li>
  <li>
   Conduct QMS training for site personnel to enhance compliance awareness.
  </li>
 </ul>
 <p>
  <strong>
   <u>
    Required Experience, Knowledge &amp; Skills
   </u>
  </strong>
 </p>
 <ul>
  <li>
   Master&rsquo;s degree in Chemistry, Applied Chemistry, Pharmaceutical Sciences (Pharm-D), or a related field.
  </li>
  <li>
   6-8 years of experience in Quality Assurance &amp; Compliance in a pharmaceutical manufacturing environment.
  </li>
  <li>
   In-depth knowledge of WHO GMP, ICH Q8, Q9, Q10, and other applicable global regulatory standards.
  </li>
  <li>
   Strong working knowledge of investigation techniques, CAPA effectiveness checks, and compliance management.
  </li>
  <li>
   Hands-on experience with QMS software tools and electronic documentation systems is preferred.
  </li>
  <li>
   Excellent analytical, communication, and documentation skills.
  </li>
  <li>
   Ability to work independently and collaboratively in a fast-paced environment.
  </li>
  <li>
   Detail-oriented with a strong compliance and continuous improvement mindset.
  </li>
 </ul>
 <p>
 </p>
</div>


Assistant Manager QA-QMS

Imtiaz Group (SMC Private) Ltd.

<p><b>Key Responsibilities:</b></p><ul><li>Develop, implement, and monitor quality assurance systems and processes for all product categories.</li><li>Lead a cross-functional quality team, ensuring effective collaboration with procurement, operations, merchandising, and supply chain departments.</li><li>Conduct regular audits and inspections across stores, warehouses, and supplier sites.</li><li>Oversee food safety management, hygiene standards, and compliance with local regulatory requirements (PSQCA, ISO, etc.).</li><li>Establish benchmarks for product quality and drive continuous improvement initiatives.</li><li>Manage quality documentation, incident reporting, and root cause analysis for non-conformities.</li><li>Train and develop store-level teams to maintain consistent quality standards.</li><li>Collaborate with vendors and internal teams to enhance product quality and minimize customer complaints.</li></ul><p><b>Requirements:</b></p><ul><li>Bachelor&rsquo;s or Master&rsquo;s degree in <b>Food Science, Quality Management, Industrial Engineering</b>, or a related field.</li><li>Minimum <b>8&ndash;10 years of experience</b> in quality assurance, preferably within <b>retail, FMCG, or manufacturing</b>.</li><li>Strong leadership, analytical, and decision-making abilities.</li><li>Thorough understanding of <b>food safety systems (HACCP, ISO 22000, GMP)</b> and <b>non-food quality standards</b>.</li><li>Excellent communication and reporting skills.</li></ul><p>Job Type: Full-time</p><p>Ability to commute/relocate:</p><ul><li>Karachi: Reliably commute or planning to relocate before starting work (Required)</li></ul><p>Work Location: In person</p>

Head - Quality Assurance (Retail/FMCG)

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Head - Quality Assurance (Retail/FMCG)