senior manager quality assurance

Fossphorus Software House

<p><b>Position:</b> Senior Manager &ndash; Audit &amp; Assurance</p><p>We are looking for a highly experienced and dynamic <b>Senior Manager &ndash; Audit &amp; Assurance</b> to join our team. The ideal candidate will have strong expertise in external audit, client management, and team leadership.</p><p><b>Experience Required:</b></p><ul><li>7&ndash;9 years of overall experience</li><li>Minimum 5 years in <b>external audit</b></li></ul><p><b>Qualification:</b></p><ul><li>Qualified <b>CA</b> or <b>CA Finalist</b></li></ul><p><b>Key Responsibilities:</b></p><ul><li>Lead and manage audit and assurance engagements from planning to completion</li><li>Review financial statements and ensure compliance with applicable standards</li><li>Manage client relationships and act as a key point of contact</li><li>Supervise and mentor team members to maintain high-quality deliverables</li><li>Ensure timely completion of assignments and adherence to deadlines</li><li>Provide technical guidance on audit and accounting matters</li><li>Lead and manage statutory and external audit engagements</li><li>Review audit working papers and ensure quality standards</li><li>Coordinate with clients for audit planning and execution</li><li>Ensure compliance with applicable accounting and auditing standards</li><li>Present audit findings and recommendations to management</li><li>Independently manage a portfolio of clients</li><li>Allocate assignments and ensure timely completion</li></ul><p><b>Skills Required:</b></p><ul><li>Strong knowledge of audit and assurance practices</li><li>Excellent leadership and team management skills</li><li>Good communication and stakeholder management</li><li>Strong analytical and problem-solving abilities</li></ul><p>Interested candidates can send their resume to: talent@fsiddiqi.com and CC:rjaved@fsiddiqi.com with Subject Line: Application for Senior Manager. - Audit and Assurance</p><p>Job Type: Full-time</p><p>Pay: Rs350,000.00 - Rs500,000.00 per month</p><p>Work Location: In person</p>

Senior Manager - Audit and Assuarance

United King

<p>United King Foods is hiring a <b>Quality Assurance Officer</b> for our food manufacturing facilities in Karachi. This role is ideal for Food Technologist candidate with experience in <b>FMCG, Food Production, Quality Assurance (QA), and Quality Control (QC)</b> who are confident working in a factory environment. Male preferred due to shift timings</p><p><b>Key Responsibilities</b></p><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><p><b>Requirements</b></p><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><p><b>Why Join Us?</b></p><ul><li>Established FMCG brand</li><li>Growth opportunities in manufacturing quality operations</li><li>Structured and performance-driven environment</li></ul><p><b>Location:</b><br/>Shafiq More<br/>Sweet Factory - Karimabad</p><p><b>Note:</b> This is a factory-based role requiring regular presence on the production floor.</p><p>Job Type: Full-time</p><p>Pay: Rs50,000.00 - Rs60,000.00 per month</p><p>Application Question(s):</p><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><p>1) Karimabad<br/>2) Shafiq More</p><p>Work Location: In person</p>

Senior Officer/ Officer - Quality Assurance

FMCG

<p>Quality Assurance &amp; Control</p><ul><li>Develop and implement quality standards, policies, and procedures</li><li>Monitor product/service quality and ensure compliance with internal benchmarks</li><li>Identify quality gaps and implement corrective and preventive actions (CAPA)</li></ul><p>Compliance &amp; Regulatory Management</p><ul><li>Ensure compliance with applicable laws, regulations, and company policies</li><li>Monitor adherence to SOPs and internal controls</li><li>Keep updated with regulatory changes and ensure timely implementation</li></ul><p>Risk Control &amp; Internal (RCI)</p><ul><li>Identify operational and compliance risks and recommend mitigation strategies</li><li>Strengthen internal control systems and governance frameworks</li><li>Conduct risk assessments and compliance reviews</li></ul><p>Audits &amp; Inspections</p><ul><li>Plan and conduct internal audits across departments</li><li>Coordinate with external auditors and regulatory bodies</li><li>Ensure timely closure of audit observations and findings</li></ul><p>Reporting &amp; Documentation</p><ul><li>Prepare compliance and quality reports for management review</li><li>Maintain accurate documentation of policies, procedures, and audit records</li><li>Track KPIs and compliance metrics</li></ul><p>Cross-Functional Coordination</p><ul><li>Work closely with operations, HR, and other departments to ensure compliance</li><li>Conduct awareness sessions and trainings on quality and compliance standards</li><li>Support process improvement initiatives</li></ul><p>Required Skills</p><ul><li>Strong knowledge of quality management systems and compliance frameworks</li><li>Experience in risk assessment and internal controls</li><li>Audit and documentation expertise</li><li>Analytical and problem-solving skills</li><li>Strong communication and stakeholder management</li></ul><p>Qualifications</p><ul><li>Bachelor&rsquo;s or Master&rsquo;s degree in Business Administration, Quality Management, or related field</li><li>Professional certifications (e.g., ISO, Compliance, Risk Management) preferred</li></ul><p>Job Type: Full-time</p><p>Pay: From Rs150,000.00 per month</p><p>Work Location: In person</p>

Deputy Manager Quality

Getz Pharma

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   Position Summary:
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  To lead Qualification and Computerized System Validation (CSV) activities across the facility. The incumbent will be responsible for overseeing equipment and utilities qualification, ensuring full compliance with regulatory standards such as WHO and PIC/S, and driving a culture of quality and continuous improvement. This role also involves implementing the Qualification Review Program (QRP) across all sites, harmonizing validation practices, and strengthening the CSV framework. Additionally, will play a key role in developing and enhancing the capabilities of validation personnel through structured competency frameworks, while ensuring efficient execution of validation strategies aligned with organizational objectives.
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   Job Responsibilities:
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   Lead and manage end-to-end qualification and CSV activities, including planning, execution, and lifecycle management of equipment, utilities, and computerized systems.
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   Develop and implement validation strategies in line with regulatory requirements and industry best practices.
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   Ensure compliance with applicable guidelines (WHO, PIC/S) and internal quality standards.
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   Review and approve Validation Master Plans (VMP), qualification protocols (DQ, IQ, OQ, PQ), reports, SOPs, and related documentation in accordance with Good Documentation Practices (GDP).
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   Oversee commissioning and qualification of new equipment, utilities, HVAC systems, water systems, and gases.
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   Coordinate cross-functional teams (Engineering, Production, QA, IT) to ensure smooth execution of validation and qualification activities.
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   Establish and drive the Qualification Review Program (QRP) across all sites to ensure ongoing compliance and requalification.
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   Lead harmonization and continuous improvement of Computerized System Validation (CSV/CSA) processes across the organization.
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   Identify gaps, implement corrective and preventive actions (CAPA), and support change control and risk assessment activities within the QMS framework.
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   Monitor project timelines, allocate resources effectively, and ensure timely completion of validation deliverables.
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   Act as Subject Matter Expert and provide technical guidance, training, and mentorship to validation team members.
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   Support internal and external audits by ensuring readiness of validation documentation and addressing audit observations.
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   Drive process optimization initiatives and contribute to overall operational efficiency (OEE improvement).
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   Required Qualification, Knowledge and Skills:
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   Pharm-D or Master&rsquo;s degree in Chemistry, Applied Chemistry, or a related scientific / Engineering discipline from an HEC-recognized university.
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   8&ndash;10 years of overall experience in validation, qualification, or quality assurance within a pharmaceutical or biotech manufacturing environment, including 2&ndash;3 years in a managerial or leadership role overseeing cross-functional teams, managing multiple validation projects, and ensuring timely execution of validation strategies.
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   Strong hands-on experience in HVAC commissioning and qualification, including system design review, installation checks, and performance verification as per regulatory requirements.
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   In-depth knowledge of water systems and process gases qualification, including generation, storage, distribution, and monitoring in compliance with GMP standards.
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   Proven expertise in cleaning validation, including development of protocols, execution, sampling strategies, and acceptance criteria.
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   Sound understanding of calibration and verification practices for instruments and equipment to ensure accuracy, reliability, and compliance.
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   Comprehensive experience in Computer System Validation (CSV/CSA), including risk-based validation approaches, system lifecycle management, and data integrity principles.
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   Demonstrated ability in process optimization and improving Overall Equipment Effectiveness (OEE) through data-driven analysis and continuous improvement initiatives.
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   Strong knowledge of Validation and Quality Management Systems (QMS), including risk assessments, change control, deviations, and CAPA management.
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   Working knowledge of AutoCAD for reviewing layouts and engineering drawings will be considered an added advantage.
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Manager – Validation & Qualification

CareCloud

<p><b>Job Overview</b></p><p>We are looking for a QA Analyst to test AI-powered voice agents through real-time call scenarios and perform detailed call audits. This role requires a combination of <b>technical understanding, analytical skills, and strong English communication</b>, as the candidate will evaluate AI conversations and system behavior.</p><p><b>Key Responsibilities</b></p><ul><li>Conduct <b>live and simulated calls in English</b> with AI voice agents</li><li>Perform detailed <b>call audits and conversation analysis</b></li><li>Identify issues such as:</li></ul><p>● Speech Recognition (ASR) errors</p><p>● Call flow and logic issues</p><p>● Delays, gaps, or incorrect responses</p><ul><li>Evaluate <b>conversation quality, tone, and user experience</b></li><li>Test workflows including:</li></ul><p>● Appointment booking</p><p>● Patient verification</p><p>● Prescription refill</p><p>● Call transfers and escalations</p><ul><li>Document findings in structured reports</li><li>Collaborate with product/dev teams to report and track issues</li></ul><p><b>Requirements (Mandatory)</b></p><ul><li><b>Strong English communication skills (spoken &amp; listening)</b></li><li>Clear pronunciation and good comprehension</li><li>Strong analytical and problem-solving skills</li><li>Attention to detail</li></ul><p><b>Preferred</b></p><ul><li>1&ndash;3 years of experience in <b>call center / QA / voice process</b></li><li>Experience in <b>call auditing / quality assurance</b></li><li>Exposure to AI or conversational systems</li></ul><p>Job Type: Full-time</p><p>Pay: Rs50,000.00 - Rs80,000.00 per month</p><p>Work Location: In person</p>

Client Services Executive (International) - QA

Official Writers

<p>Academic QA Executive (Female Only)</p><p>Official writers is looking for a talented and experienced profile for Quality Assurance officer for Academic Research Writing.</p><p><b>Responsibilities</b></p><ul><li>Proofread daily content of minimum 20,000 and maximum 40,000 academic research content</li><li>Cross-check the work is done based on learning objectives</li><li>Make sure finalized versions are formatted (TOC, Line Spacing and Alignment)</li><li>Ensure that corrections/revisions are given priority and done according to task requirements</li><li>Make sure all tasks have no grammatical, sentencing errors</li><li>All tasks are well references</li><li>Referencing standards are followed completely</li><li>Ensure write productivity is maximized</li><li>Ensure no tools are used in writing</li></ul><p><b>Requirements</b></p><ul><li>Bachelors/Master's degree.</li><li>2 Years of experience as academic writers in a reputable firm</li><li>Commendable knowledge of format, vocabulary, grammar, understanding of the assignment brief</li><li>Ensure if the task requirements are fulfilled and meet the standards of the company</li><li>Ability to produce work assignment in a given time</li><li>Job Type: Office-based (Full time)</li></ul><p>Those who are interested can send their resume on hr@officialwriters.com</p><p>Job Type: Full-time</p><p>Work Location: In person</p><p>Job Type: Full-time</p><p>Work Location: In person</p>

Academic QA Executive (Female)

Reckitt

<div></div><div><div><div><div>Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege.</div></div><div><div><h2 class="jobSectionHeader"><b>
Research &amp; Development
</b></h2></div><div>In Research and Development, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance.<br>
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We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.<br>
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The size of our organisation means you'll have the opportunity to learn and work in different functions within R&amp;D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.</div></div><div><div><h2 class="jobSectionHeader"><b>
About the role</b></h2>
</div><div><ul><li>The scope of the job includes planning and managing, day to day QA oversight activities.</li>
<li>Ensuring on time release of products from Mauripur &ndash; Healthcare/ Household after proper review.</li>
<li>Support SQH in Quality resource management, update system and documents as per requirement.</li>
<li>Direct reports include:</li>
<li><ul><li>AM QA</li>
<li>QA Executive</li>
</ul></li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Your responsibilities</b></h2>
</div><div><ul><li>Authorized by Reckitt for taking final decision on release or rejection of finished products in conjunction with SOP HCQA-017.</li>
<li>Authorized to delegate release or rejection of finished products including but not limited to as per Quality Assurance System defined under Schedule B-II GMP compliance of Drug Act 1976.</li>
<li>Authorized by Reckitt in reference to Drug Act 1976, Drug (Licensing &amp; Advertising) Rules 1976 &amp; Schedule B-II to release &amp; certify or to delegate release &amp; certify that each production batch has been produced and controlled in accordance with the requirements of the good manufacturing practices and the relevant rules made under the Ordinance relevant to the production, control, and release of drugs as well as of conditions of registration.</li>
<li>Establish the quality management system and procedures.</li>
<li>Monitor adherence to QA process is following all local regulatory requirements and Reckitt quality management systems.</li>
<li>Ensure that the quality control procedures are implemented during every step of the production process.</li>
<li>Implement Product Quality plans to ensure controls of manufacturing, quality testing and product packaging through line inspection.</li>
<li>Implement Product Validation second plan to ensure robustness of manufacturing process, equipment, cleaning, and environment.</li>
<li>Ensure that Annual Product Review (APR) are prepared and CAPA plan is in place.</li>
<li>Ensure that thorough checking of batch documents in order to ensure release of Finished Products for sales is done in compliance with all local regulatory requirements and Reckitt Quality Management System.</li>
<li>Plan and conduct internal quality audits and facilitate proactive solutions by collecting and performing statistical analysis of quality data.</li>
<li>Establish and implement the Inspection and Testing Plan</li>
<li>Participate in GMP Audit Program for the site.</li>
<li>Ensure that deviations system is in place and effective CAPA and investigations are being done and monitor progress on implementation of CAPA.</li>
<li>Ensure that Change control procedures are in place and effective.</li>
<li>Take appropriate corrective actions on identified problems.</li>
<li>Identify potential sources of error and suggest ways to eliminate them. (Preventive Actions)</li>
<li>Support in investigating customer complaints.</li>
<li>Ensure to manage proper upkeep and maintenance of Batch history records / documents and finished products and raw material retention samples.</li>
<li>Monitor and report KPIs and take corrective / Preventive actions to improve quality performance.</li>
<li>Continuous process improvement Devise procedures to inspect and report quality issues.</li>
<li>Carry out regular Quality reviews with Supply Leadership to highlight areas of risk, progress being made, help needed and learning to be transferred smoothly.</li>
<li>Ensure that NPD/EPD projects are smoothly handed over into manufacturing operations while &lsquo;Good-For-Sale&rsquo; is only approved when all quality requirements and success criteria are satisfied.</li>
<li>Any other job/task assigned by Site Quality Head.</li>
</ul></div></div><div><div><h2 class="jobSectionHeader"><b>The experience we're looking for</b></h2>
</div><div><ul><li>Doctor of Pharmacy (Pharm &ndash; D) or bachelor&rsquo;s degree in pharmacy with 7 years experience having minimum five years experience in quality control and testing of drugs.</li>
<li>Additional business high school graduation degree e.g., MBA/ MPhil will be preferred.</li>
<li>Clear understanding and ability to assess and act upon product safety, quality, efficacy, and compliance risks.</li>
<li>Good understanding of typical regulatory requirements relevant to a regulated product (But not limited to) e.g., Drugs Act. 1976, DRAP Rules 2012, ISO Standards and applicable ICH guidelines.</li>
</ul></div></div><div><div><h2 class="jobSectionHeader"><b>The skills for success</b></h2>
</div><div>Commercial Awareness, Business Partnership, Collaboration, Partnership building, Ability to challenge the status quo, Propose improvement, Accountability, Adaptability, Collaborator, R&amp;D, Product Lifecycle Management.</div></div><div><div><h2 class="jobSectionHeader"><b>
What we offer</b></h2>
</div><div>With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy.</div></div><div><div><h2 class="jobSectionHeader"><b>
Equality</b></h2>
</div><div>We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.</div></div></div></div>

Head of Quality Assurance

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