quality assurance manager Jobs in Karachi Pakistan

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assistant manager qa-qms Jobs in Karachi Pakistan

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deputy manager qms

UNITED TOWEL EXPORTERS PRIVATE LIMITED

We are hiring Deputy Manager QMSLocation: Korangi Industrial Area, Karachi.Experience: Minimum 5-8 years of relevant experience (Terry Towel industry experience will be preferred).Education: B.E/Masters/MPA/MBA or equivalent from any reputable HEC recognized University/Institute .Responsibilities:<ul><li>Strengthen QMS team to drive in overall with QMS methodologies and system.</li><li>Hands on continuous improvement process excellence and cost enhancement.</li><li>Hands on experience in lean six sigma, value stream mapping and other statistical models.</li><li>Lead developing sections of QMS for development of different levels of documents.</li><li>Train upper &amp; middle management regarding importance of audits and systems.</li></ul>Skills and Traits: <ul><li>Proficient in MS Office &amp; SAP application.</li><li>Strong organizational, Analytical, Multi tasking and problem solving skills.</li></ul>Job Type: Full-timeWork Location: In person

Deputy Manager QMS

nkc smc pvt ltd

The deputy manager has a broad range of responsibilities, including administrative duties, strategy and organizing a team. Their responsibilities and duties will also vary depending on the size of their team and the kind of industry you are hiring in. These are some areas that deputy managers might be responsible for in your team:<ul><li>Stepping in as manager when the general manager is off work or unavailable</li><li>Able to work with HR to hire and train new staff</li><li>Able to develop strategies for new projects, set deadlines and create workflows</li><li>Can delegate tasks effectively to team members while taking responsibility for the outcome</li><li>Helps team members to follow company rules and guidelines</li><li>Helps the general manager to make important decisions related to administration, projects and management procedures</li><li>Keeps records of financial and legal matters</li><li>Can summarize team activities in order to keep senior managers informed</li></ul>Job Type: Full-timePay: Rs85,000.00 - Rs100,000.00 per monthWork Location: In person

Deputy Manager Operations (Housekeeping)

<div>Site Name: Pakistan - Sindh - Karachi 
Posted Date: Nov 7 2025 
Job Purpose
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.
Education, Experience &amp; Skills<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>
Key Responsibilities<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>
Job Purpose
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.
Education, Experience &amp; Skills<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>
Key Responsibilities<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>
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>

Site Regulatory Compliance Head

Getz Pharma

<div>
 
 
 Job Responsibilities:
 
 
 <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
 
 root cause analysis (RCA)
 
 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
 
 5 Whys
 
 ,
 
 Ishikawa diagrams
 
 , 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
 
 Good Documentation Practices (GDP)
 
 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>
 
 
 
 Required Experience, Knowledge &amp; Skills
 
 
 
 <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>
 
 
</div>

Assistant Manager QA-QMS

<div>Site Name: Pakistan - Sindh - Karachi 
Posted Date: Nov 4 2025 
Job Purpose
To contribute the growth and profitability of GlaxoSmithKline through processing of Tablet products, in accordance with the compliance of GlaxoSmithKline code of GMP and to fulfil the local regulatory requirement, using all the available resources to the maximum advantage of the company and customer satisfaction.
Education, Experience &amp; Skills
<ul><li>1-3 years of experience in similar role</li><li>
Pharm-D</li><li>
QMS, EHS Training</li></ul>
Key Responsibilities
<ul><li>Discussion of daily planning and work schedule with Department Head.</li><li>
To supervise the operation involved in the following areas:</li><li>
Compression, Coating, Granulation, Dispensing &amp; Blistering</li><li>
To ensure the follow up of production activities as per given production schedule by Planning department in order to achieve site plan</li><li>
Support other functions by providing necessary help, and good customer services to relevant departments.</li><li>
Maintain cordial relationships with all stakeholders within the organization for fulfillment of the site goal.</li><li>
To supervise the manufacturing operations in Production Department.</li><li>
Checks and maintain the all relevant records of manufacturing section.</li><li>
To maintain and ensure the delivery of batch related documents in a timely manner.</li><li>
To prepare and complete all documentation applicable to dispensing and manufacturing by receiving, checking, and reconciliation of materials.</li><li>
To maintain SAP data postings (Inventory transactions, labor hour distribution).</li><li>
To maintain standard operating procedure, as necessary coordinate with Engineering for preventive and breakdown maintenance of production equipment.</li><li>
To gain professional and technical knowledge by attending EHS, QMS and GMP trainings at the site and through my learning.</li><li>
To ensure compliance with GMP and QMS within department by applying GQMP&rsquo;s.</li><li>
To provide in house trainings of SOPs &amp; BMRs to relevant staff.</li><li>
To ensure that QMS is in-place and in-use in concerned area of responsibility.</li></ul>
Job Purpose
To contribute the growth and profitability of GlaxoSmithKline through processing of Tablet products, in accordance with the compliance of GlaxoSmithKline code of GMP and to fulfil the local regulatory requirement, using all the available resources to the maximum advantage of the company and customer satisfaction.
Education, Experience &amp; Skills
<ul><li>1-3 years of experience in similar role</li><li>
Pharm-D</li><li>
QMS, EHS Training</li></ul>
Key Responsibilities
<ul><li>Discussion of daily planning and work schedule with Department Head.</li><li>
To supervise the operation involved in the following areas:</li><li>
Compression, Coating, Granulation, Dispensing &amp; Blistering</li><li>
To ensure the follow up of production activities as per given production schedule by Planning department in order to achieve site plan</li><li>
Support other functions by providing necessary help, and good customer services to relevant departments.</li><li>
Maintain cordial relationships with all stakeholders within the organization for fulfillment of the site goal.</li><li>
To supervise the manufacturing operations in Production Department.</li><li>
Checks and maintain the all relevant records of manufacturing section.</li><li>
To maintain and ensure the delivery of batch related documents in a timely manner.</li><li>
To prepare and complete all documentation applicable to dispensing and manufacturing by receiving, checking, and reconciliation of materials.</li><li>
To maintain SAP data postings (Inventory transactions, labor hour distribution).</li><li>
To maintain standard operating procedure, as necessary coordinate with Engineering for preventive and breakdown maintenance of production equipment.</li><li>
To gain professional and technical knowledge by attending EHS, QMS and GMP trainings at the site and through my learning.</li><li>
To ensure compliance with GMP and QMS within department by applying GQMP&rsquo;s.</li><li>
To provide in house trainings of SOPs &amp; BMRs to relevant staff.</li><li>
To ensure that QMS is in-place and in-use in concerned area of responsibility.</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>

Production Officer

Unity Foods Limited

We are looking for a Deputy Manager &ndash; Reporting to join our Finance team. The role involves supporting monthly and periodic financial closing, preparing management reports, and ensuring compliance with accounting standards and audit requirements.Key Responsibilities:Lead monthly and annual financial closing activities.Prepare management accounts, financial statements, and supporting schedules.Review and reconcile ledgers, accruals, and adjustments.Liaise with auditors during reviews and audits.Ensure accuracy of financial reporting in SAP.Requirements:ACCA / CIMA qualified or CA (Part-Qualified).7 to 8 years of relevant experience.SAP and manufacturing industry experience preferred.Strong analytical, reporting, and communication skills.Job Type: Full-timePay: Rs100,000.00 - Rs300,000.00 per monthWork Location: In person

Deputy Manager – Reporting

Zedco

Key Responsibilities* Develop and implement end-to-end supply chain strategies to improve efficiency and reduce costs.* Manage procurement, inventory, warehousing, and logistics to ensure timely delivery of goods.* Establish strong vendor relationships and negotiate favorable terms to maximize value.* Monitor supply chain performance using KPIs and analytics, ensuring continuous improvement.* Lead a team and foster a culture of excellence and accountability.Skills and Competencies:* Excellent analytical, negotiation, and communication skills.* Proficient in MS Office.Education:At least Masters in Supply Chain ManagementExperience* Relevant experience of 1 year in a similar roleApply Now!Send your resume to hr@zedco.org with the subject line &quot; Deputy Manager&quot; latest 25 Oct 2025Job Type: Full-timeWork Location: In person

Deputy Manager Supply Chain

Explore 476+ Deputy manager qms in Karachi Pakistan this November. Find roles across top companies and apply now to boost your career.