manager of quality

هيئة التأمين | Insurance Authority

<div>
 <p>
  Job Purpose:
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   The Manager of Data Quality &amp; Monitoring is responsible for ensuring the accuracy and reliability of data across the Insurance Authority&rsquo;s systems. This role establishes robust data quality validation frameworks, monitors data integrity in real time, and leads the development of reference data and metadata systems. The position plays a critical role in regulatory compliance, business continuity, and the operational effectiveness of the Insurance Data Hub.
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  Key Responsibilities and Activities
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 </p>
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  <strong>
   Operations Management :
  </strong>
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  Implement the policies, regulations, procedures, and controls so that all relevant procedural/ legislative requirements are met while delivering high-quality and cost-effective results.
 </p>
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  <br/>
 </p>
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  <strong>
   Data Quality &amp; Monitoring :
  </strong>
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  Data Quality Assurance &amp; Validation
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  <li>
   Develop and implement automated data validation processes to identify and prevent data errors, inconsistencies, and missing records.
  </li>
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   Define and monitor data quality metrics, thresholds, and KPIs through dashboards and reports.
  </li>
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   Collaborate with Data Engineering &amp; Storage teams to resolve data integrity issues at the storage level.
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   Escalate persistent or high-risk data quality issues to Governance, Risk, and Compliance (GRC) and relevant business units, particularly where regulatory reporting is impacted.
  </li>
 </ul>
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  Data Monitoring &amp; Issue Resolution
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   Establish real-time monitoring systems to detect data anomalies, unauthorized changes, and discrepancies.
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   Implement alerting mechanisms for critical data quality breaches requiring immediate response.
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   Coordinate with IT and analytics functions to ensure clean, verified datasets are available for operational and strategic use.
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   Contribute to crisis management efforts by validating datasets and facilitating rollbacks to trusted data sources when needed.
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   Identify and document root causes of recurring data quality issues affecting reporting or supervisory accuracy.
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 </ul>
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  Compliance &amp; Governance Alignment
 </p>
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  <li>
   Align data quality policies and practices with frameworks defined by the Data Governance Office.
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   Support audit readiness and regulatory compliance by maintaining validated datasets and documentation.
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   Maintain up-to-date documentation of data validation rules, historical issues, quality thresholds, and resolution actions.
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  Reference &amp; Master Data (RMD) Management
 </p>
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  <li>
   Lead the development and implementation of a strategic approach to reference and master data management.
  </li>
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   Define and maintain standards, governance policies, and lifecycle procedures for key data domains.
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   Ensure the integration of reference and master data across systems, including the Insurance Data Hub.
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   Collaborate with internal stakeholders to harmonize and institutionalize RMD practices.
  </li>
 </ul>
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  Metadata and Data Cataloging
 </p>
 <ul>
  <li>
   Design and execute metadata frameworks to document, organize, and classify data assets within the Insurance Data Hub.
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   Build and maintain a comprehensive data catalog that improves data discoverability, transparency, and reuse.
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   Work with technical and business teams to ensure metadata remains up-to-date and aligned with evolving data assets and systems.
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   Perform other activities as and when required.
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 </p>
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  Qualifications and Requirements
 </p>
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  <br/>
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  Knowledge and Experience :
 </p>
 <ul>
  <li>
   8+ years or more of relevant experience in data quality management, metadata, or any relevant field.
  </li>
  <li>
   Previous experience in in data pipeline tools (e.g., Apache Airflow, Talend), storage platforms (e.g., Hadoop, cloud data lakes), and integration technologies (e.g., APIs, ETL frameworks).
  </li>
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   Strong understanding of reference/master data, data cataloging tools, and data quality automation frameworks.
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   Experience with regulatory or audit environments, particularly in public or financial sectors.
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   Hands-on knowledge of data monitoring tools, metadata repositories, and data quality metrics.
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  <br/>
 </p>
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  Education and Certifications
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  <li>
   Bachelor&rsquo;s degree in Data Management, Information Systems, Computer Science, or a related field.
  </li>
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   Relevant certification is preferred
  </li>
 </ul>
</div>


Manager of Data Quality & Monitoring

AEG Consulting

<p><b>Position Overview</b></p><p>The Manager of Quality Control (QC) &amp; Quality Assurance (QA) leads the factory&rsquo;s quality function for medical devices and disposables (bandages, masks, medical tapes, and related products). This role ensures full compliance with Drug Regulatory Authority of Pakistan (DRAP) Medical Device Rules 2017, Good Manufacturing Practices for Medical Devices (GDPMD), and ISO 13485 Quality Management Systems. The position oversees quality testing, assurance systems, audits, regulatory compliance, and continuous improvement of product quality and safety.</p><p><b>Key Responsibilities</b></p><p><b>1. Regulatory &amp; Compliance Oversight:</b></p><ul><li>Ensure all quality systems comply with DRAP Medical Device Rules 2017 and ISO 13485 requirements.</li><li>Maintain valid DRAP certifications, licenses, and product registrations for all manufactured devices.</li><li>Prepare and manage documentation required for DRAP audits, GMP/GDPMD inspections, and ISO audits.</li><li>Liaise with regulatory bodies (DRAP, MoH) during inspections, ensuring timely responses to observations.</li></ul><p><b>2. Quality Assurance (QA):</b></p><ul><li>Develop, implement, and maintain SOPs for all production and quality processes.</li><li>Oversee validation and qualification activities (equipment, processes, and cleanrooms).</li><li>Ensure all raw materials, in-process checks, and finished goods comply with quality and regulatory requirements.</li><li>Lead Corrective and Preventive Actions (CAPA) for deviations and non-conformities.</li><li>Ensure proper implementation of Document Control and Change Control systems.</li></ul><p><b>3. Quality Control (QC):</b></p><ul><li>Oversee laboratory and in-process QC testing for raw materials, intermediates, and finished products.</li><li>Monitor and report number of quality issues per month and ensure corrective actions.</li><li>Validate and maintain testing methods for accuracy, reliability, and compliance with device standards.</li><li>Ensure calibration and maintenance of laboratory instruments.</li><li>Review and approve Certificates of Analysis (CoA) and release of finished goods.</li></ul><p><b>4. Risk Management &amp; Safety:</b></p><ul><li>Implement risk-based quality management in line with ISO 14971 (Risk Management for Medical Devices).</li><li>Ensure hygienic, contamination-free production environments through audits and inspections.</li><li>Work with the Operations Manager to maintain a Zero Total Recordable Incident Rate (TRIR) and maximize safe man-hours.</li></ul><p><b>5. Audits &amp; Inspections:</b></p><ul><li>Lead internal quality audits to ensure compliance with GDPMD, ISO 13485, and DRAP requirements.</li><li>Coordinate management reviews and ensure continuous improvement of the QMS.</li><li>Lead preparation for DRAP and ISO surveillance audits, ensuring audit readiness across departments.</li></ul><p><b>6. Team Leadership &amp; Training:</b></p><ul><li>Manage and mentor QC/QA staff to build strong technical and compliance capabilities.</li><li>Conduct regular training sessions for production and QC/QA teams on GDPMD, GMP, ISO 13485, hygiene, and quality standards.</li><li>Foster a culture of quality, accountability, and regulatory compliance across the organization.</li></ul><p><b>7. KPI Monitoring &amp; Reporting:</b></p><ul><li>Track and report the following KPIs regularly:</li><li>Number of quality issues per month in QC checks.</li><li>CAPA closure rate and lead time.</li><li>Audit observations vs. compliance closures.</li><li>Planned vs. Actual product release timelines.</li><li>% of batches released without deviation.</li><li>Material rejection rate &le;1% (in line with wastage targets).</li><li>Submit quality performance reports to senior management and regulatory bodies where required.</li></ul><p><b>Education &amp; Experience Requirements:</b></p><ul><li>Bachelor&rsquo;s or Master&rsquo;s in Pharmacy, Microbiology, Biomedical Engineering, or related field.</li><li>Minimum 8&ndash;12 years&rsquo; experience in QC/QA within medical devices or pharmaceutical manufacturing, including at least 3 years in a leadership role.</li><li>In-depth knowledge of DRAP Medical Device Rules 2017, GDPMD, ISO 13485, and ISO 14971.</li><li>Strong background in laboratory management, audits, and regulatory compliance.</li></ul><p><b>Key Skills &amp; Competencies:</b></p><ul><li>Expertise in quality systems (QMS), validation, and compliance.</li><li>Strong leadership in audit handling (internal &amp; external).</li><li>Proficiency in CAPA, deviation handling, and root cause analysis.</li><li>Excellent documentation, reporting, and regulatory communication skills.</li><li>Analytical and problem-solving skills with a focus on continuous improvement.</li></ul><p>Job Type: Full-time</p><p>Pay: Rs125,000.00 - Rs175,000.00 per month</p><p>Work Location: In person</p>

Manager of QA/QC – Medical Devices Manufacturing (DRAP Compliance)

Aptean

<div><div><ul><li>India</li><li>
5874</li><li>
Employee Regular Full Time</li></ul></div><div></div><div><h2 class="jobSectionHeader"><b>
Job Description
</b></h2><div>Overview<div></div><div><b><br>
Location Bangalore</b></div><div></div><div><br>
Aptean is changing. Our bespoke ERP solutions are transforming a huge range of global businesses, from food producers to manufacturers. In a world of generic enterprise software, we provide targeted solutions that bring together the very best technology and drive greater results. With over 4500 employees, 90 different products and a global client base, there&rsquo;s no better time to advance your career at Aptean.</div><div></div><p><b><br>
The Who, What, Where and Why</b></p><p>
As a Manager of Quality Engineering, you will play a key role in driving exceptional levels of quality and testing efficiency within our products, while simultaneously partnering with other teams within Research and Development to ensure delivery objectives are consistently achieved. This role is designed for individuals who have a solid foundation in quality engineering, testing, and leadership, and are eager to contribute their skills to enhance rapid delivery of enterprise supply chain solutions. You will collaborate with cross-functional teams and utilize both your technical expertise and leadership skills to contribute to the overall success of our organization. You will be a strategic partner, mentor, and facilitator, enabling the Scrum teams to take ownership of quality and deliver high-quality products efficiently.</p><p></p><p><b><br>
Who?</b></p><p><b>
We&rsquo;d</b><b> like this person to have the following skills/abilities:</b></p><ul><li>
Bachelor&rsquo;s degree in computer science, engineering, or a related field</li></ul><ul><li>
Demonstrable experience as a QA Manager, Lead, or similar role, with 7+ years in quality assurance and at least 2 years in a management position</li></ul><ul><li>
Proven experience managing distributed QA teams, including training, performance management, and team development</li></ul><ul><li>
Deep knowledge of quality engineering methodologies, tools, and frameworks</li></ul><ul><li>
Hands-on experience with software testing, defect tracking, and quality management systems (e.g., JIRA, Zephyr, Azure DevOps, TestRail, and Quality Centre)</li></ul><ul><li>
Background in developing and managing automated test suites using tools such as Selenium WebDriver, TestNG, QTP, or similar, and scripting languages</li></ul><ul><li>
Demonstrated ability to utilize expert knowledge of Agile/Scrum methodology and processes to shift left in testing and identify defects earlier in the delivery cycle.</li></ul><ul><li>
Excellent leadership, problem-solving, and communication skills, with the ability to present complex information to various stakeholders</li></ul><ul><li>
CI/CD knowledge preferred</li></ul><ul><li>
Familiarity with AI test tools a plus</li></ul><p></p><p><b><br>
What?</b></p><p><b>
In this role, you would:</b></p><ul><li>
Collaborate with cross-functional teams to ensure timely releases that meet and exceed quality expectations</li></ul><ul><li>
Support QE efforts across multiple product lines and scrum teams</li></ul><ul><li>
Use subject matter expertise to guide scrum teams in creating comprehensive test strategies and plans, including manual and automated testing, performance testing, and security testing</li></ul><ul><li>
Provide technical guidance, training, and mentorship to QEs within the Scrum teams, helping them stay up-to-date with the latest tools, technologies, and testing techniques</li></ul><ul><li>
Act as a central point of contact for quality-related issues, helping to resolve conflicts and facilitate effective communication between Scrum teams, product owners, and other stakeholders</li></ul><ul><li>
Monitor key quality metrics (e.g., defect density, test execution rate, code coverage, etc.) across all Scrum teams to track progress, identify areas for improvement, and report on the overall product quality</li></ul><ul><li>
Assist teams in identifying and implementing process improvements through retrospectives and data analysis, to ensure ongoing enhancement of QE practices and team effectiveness</li></ul><ul><li>
Drive shift-left strategies to identify defects and quality risks earlier in the delivery process</li></ul><div><b><br>
What&rsquo;s in it for you?</b><br>
Aptean offers competitive pay and robust benefit plans along with the opportunity to
<br>
grow your career in a fast-paced, flexible and casual environment, an outstanding
<br>
opportunity for career development and growth.<br>
<br>
<b>About Aptean</b><br>
At Aptean, our mission is to solve tomorrow&rsquo;s unique challenges today with unrivaled,
<br>
purpose-built software and superior customer experiences from people who care.
<br>
Aptean is a global provider of mission-critical, industry-specific software solutions.
<br>
Aptean&rsquo; s purpose-built ERP and supply chain management solutions help address the
<br>
unique challenges facing process and discrete manufacturers, distributors and other
<br>
focused organizations. Aptean&rsquo; s compliance solutions are built for companies serving
<br>
specific markets such as finance, healthcare, biotech and pharmaceuticals, over 10,000
<br>
highly specialized organizations in more than 20 industries and 80 countries rely on
<br>
Aptean to streamline their everyday operations.<br>
<br>
&ldquo;At Aptean, our global and diverse employee base is our greatest asset. It is through
<br>
embracing and understanding our differences that we are able to harness our individual
<br>
power to maximize the success of our customers, our employees and our company.&rdquo; &ndash;<br>
TVN Reddy<br>
<br>
<i>Aptean pledges to promote a company culture where diversity, equity and inclusion are
</i><br>
<i>central. We are committed to applying this principle as we interact with our customers,
</i><br>
<i>build our teams, cultivate our leaders and shape a company in which any employee can
</i><br>
<i>succeed, regardless of race, color, sex, national origin, sexuality and gender identity,
</i><br>
<i>religion, disability or age. Celebrating our diverse experiences, opinions and beliefs
</i><br>
<i>allows us to embrace what makes us unique and to use this as an asset in bringing
</i><br>
<i>innovative solutions to our customer base.</i></div></div></div></div>

Manager,QA

Accor

<p><b>Position Overview:</b><br/>The Quality &amp; Hygiene Manager is responsible for ensuring that all products and processes meet the highest standards of quality and hygiene. This role involves developing, implementing, and monitoring quality control and hygiene programs to maintain compliance with industry regulations and company policies.</p><p><b>Key Responsibilities:</b></p><ul><li>Develop and maintain quality assurance and hygiene protocols to comply with legal, regulatory, and company standards.</li><li>Conduct regular audits and inspections of production areas to ensure compliance with hygiene and quality standards.</li><li>Lead training programs for staff on quality control and hygiene best practices.</li><li>Investigate quality or hygiene issues, identify root causes, and implement corrective actions.</li><li>Collaborate with production, procurement, and other departments to ensure quality standards are maintained.</li><li>Prepare reports and documentation related to quality and hygiene performance.</li><li>Stay updated with industry trends, regulations, and technologies related to quality and hygiene management.</li><li>Manage compliance with certifications such as ISO, HACCP, GMP, or others relevant to the industry.</li></ul><p><b>Qualifications:</b></p><ul><li>Bachelor&rsquo;s degree in Food Science, Microbiology, Quality Management, or related field (preferred).</li><li>Proven experience in quality and hygiene management, preferably in manufacturing, food production, or healthcare sectors.</li><li>Strong knowledge of regulatory requirements and industry standards.</li><li>Excellent problem-solving and analytical skills.</li><li>Effective communication and training abilities.</li><li>Attention to detail and strong organizational skills.</li></ul><p>Job Types: Full-time, Permanent</p>

Quality & Hygiene Manager

<div><p><b>Title:</b></p>
Manager, Quality<p></p><p><b><i>
&quot;Belong, Connect, Grow, with KBR!
</i></b></p><p></p><p><b><i>The KBR team of teams delivers future-forward science, technology and engineering solutions and mission-critical services that help governments and companies around the world accomplish their most important objectives, while also helping achieve their sustainability goals.</i></b></p><p></p><p><b><i>
KBR Sustainable Technology Solutions provides holistic and value-added solutions across the entire asset life cycle. These include world-class licensed process technologies, differentiated advisory services, deep technical domain expertise, energy transition solutions, high-end design and engineering capabilities, and smart solutions to optimize planned and operating assets.&quot;</i></b></p><p></p><p><b>
Job Requirement</b></p><p></p><p>
KBR is looking for <b>Manager, Quality </b>with <b>Gas Processing &amp; Gas Compression</b> experience to be based in <b>Sharjah</b> for a <b>PMC project.</b></p><p></p><p><b>
Experience required:</b></p><p></p><ul><li>
Minimum Overall 20+ years of oil &amp; gas experience.</li><li>
Experience within FEED &amp; Detail Engineering experience.</li><li>
Experience in ADNOC Projects involving Gas Processing plants, pipelines etc.&hellip;</li><li>
Must have at least 10+ Years experience working in Onshore and offshore projects.</li><li>
Bachelor&rsquo;s degree in engineering is a MUST.</li></ul><p></p><p>
Interested and suitable candidates please apply for the role. Suitable candidates will be contacted directly.</p></div><p></p>

Manager, Quality

Fatima Memorial Hospital

<p>Fatima Memorial Hospital College of Medicine &amp; Dentistry is a 470 bed, multi-specialty, tertiary care teaching institution. Fatima Memorial Dental Hospital is an affiliate of Fatima Memorial Hospital College of Medicine &amp; Dentistry and recognized for Undergraduate and Postgraduate Training by the College of Physicians &amp; Surgeons of Pakistan in all major disciplines. It offers state of the art clinical &amp; diagnostic services through clinical experts to patients from all walks of life.</p><p><b>Manager Quality Enhancement Cell (QEC):</b></p><p><b>Qualification and Experience:</b> Post Graduation degree with specialization in Quality Assurance and having at least 5 years&rsquo; experience of QA/QEC at any Medical College/ HEC recognized university.</p><p>Strong Interpersonal, analytical, communication and computer skills will be highly preferred.</p><p>&#61623; Manager QEC will define clear and explicit standards of academic learning.</p><p>&#61623; To develop program specifications. These are standard set of information clarifying what knowledge, understanding, skills and other attributes a student will develop on successfully completing a specific program.</p><p>&#61623; To develop quality assurance processes and methods of evaluation to affirm that the quality of provision and the standard of awards are being maintained and to foster curriculum, subject and staff development, together with research and other scholarly activities.</p><p>&#61623; To ensure that the College&rsquo;s quality assurance procedures are designed to fit in with the arrangements in place nationally for maintaining and improving the quality of Medical Education.</p><p>&#61623; The incumbent will discharge his/her responsibilities under the supervision and guidance of Principal FMH CM&amp;D.</p><p>Job Type: Full-time</p><p>Work Location: In person</p>

Manager QEC

L&T Technology Services Ltd.

<div><div><div>Manager - QA/QC</div><p>LNT/M/1442617</p><ul>
PTD-Power Transmission &amp; Distribution - ICDamam, SA</ul></div><div><div><div><ul><div><div><div>
Posted On</div><div>
18 Aug 2025</div></div></div><div><div><div>
End Date</div><div>
14 Feb 2026</div></div></div><div><div><div>
Required Experience</div><div>
15 - 20 Years</div></div></div></ul></div></div></div></div>
<br><div><div><div>Skills</div></div><div><div><p>
Knowledge &amp; Posting Location</p><div><p>
QUALITY CONTROL
</p><p>QUALITY MANAGEMENT
</p><p>ISO
</p><p>INSPECTION
</p><p>QUALITY ASSURANCE
</p></div></div><div><p>Minimum Qualification</p><div><p>
BACHELOR OF ENGINEERING (BE)</p><p>
BACHELOR OF TECHNOLOGY (BTECH)</p></div></div></div></div>
<br><div><div><div>Job Description</div></div><p></p><div><br>
<ul><li>
Study the approved drawings, material/equipment approvals, and technical specifications, standards etc. required for the project and implement the same as applicable.</li><li>
Draft and finalize Project Quality Assurance Plan (PQAP) for the assigned project</li><li>
Establish Inspection and Test Plan (ITP) and checklists for various construction activities of project and ensure its implementation.</li><li>
Obtain customer approval of various quality documents from internal /customer representative and coordinate &amp; implement the same across the project.</li><li>
Review and edit method statements in consultation with Construction Manager/Site Engineers for various construction activities.</li><li>
Raise / ensure work/material/equipment Inspection Requests (IR) as per contract requirements / ITPs on time and on regular basis.</li><li>
Ensure all quality requirements of projects of subcontracted works (document/ approvals/inspections/other).</li><li>
Coordinate with site team for arranging inspections/ tests and close out of comments</li><li>
Ensure the preparation, review, approval and maintenance of all documents / records of quality function in traceable way.</li><li>
Conduct orientation/ training / quality promotion programs as required on project.</li><li>
Raise Non-Conformance Reports (NCR) for any deviations and also follow up for necessary corrective actions to close the NCRs.</li><li>
Provide supervision, guidance, and technical support</li></ul></div></div><p></p>

Manager - QA/QC

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