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assistant manager qa qms

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

Techno Cloud Pvt. Ltd.

Responsibilities<ul><li>Perform QA/QC inspection of incoming material and maintain records.</li><li>Inspect and verify electrical, mechanical, and mechatronics jobs for FTI/VEY operations and project executions.</li><li>Conduct PO acceptance for customer POs and PO verification for FTI POs.</li><li>Visit fabrication workshops for inspection of mechanical/electrical jobs; ensure record keeping.</li><li>Visit client sites for inspection of jobs.</li><li>Perform material verification and dimensional checks at port/vendor sites with documentation.</li><li>Ensure all design and execution follows relevant international codes and standards.</li><li>Prepare and implement QIP (Quality Inspection Plans) and ITP (Inspection Test Plans) for project jobs.</li><li>Supervise DT/NDT, IP/current/continuity/megger tests as required.</li><li>Assist in FAT (Factory Acceptance Test) and commissioning activities for projects.</li><li>Monitor plant operational parameters, condition of accessories, and safety compliance at client sites; prepare reports.</li><li>Assist in other QA/QC inspection and monitoring tasks as required.</li></ul>Other Relevant Tasks / Authorities<ul><li>Assist in the development and implementation of Quality Management System (QMS) within the organization.</li><li>Monitor and ensure implementation of safety policies across operations.</li><li>Support data feeding/reporting for FTI plant operational parameters and production volumes.</li><li>Promote continuous improvement in QC processes and compliance.</li></ul>Qualifications &amp; Skills<ul><li>Education: BE in Mechatronics</li><li>Certifications (Preferred): Relevant ISO certifications.</li><li>Experience: 2&ndash;3 years in fertilizer, water treatment, or energy sector (QA/QC or inspection role).</li><li>Technical Knowledge:</li><li>Electrical systems: continuity, insulation resistance, current rating, IP rating tests.</li><li>Mechanical systems: stress analysis, hydrotest, NDT.</li><li>Material verification, dimensional inspection, and use of measuring instruments.</li><li>QIP/ITP preparation, QMS understanding, compliance reporting.</li><li>Soft Skills: Strong communication, problem-solving, documentation, and team collaboration.</li></ul>Job Type: Full-timePay: Rs80,000.00 per monthWork Location: In person

QA Engineer - Compliance

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

Confiz

<div>We are seeking an experienced QA Automation Engineer with a strong background in Katalon Studio to join our Quality Engineering team. The ideal candidate will have hands-on experience designing, developing, and maintaining automated test frameworks, ensuring product quality through rigorous test automation, and working closely with cross-functional teams in Agile environments.
Responsibilities:
<ul><li>Design, develop, and maintain robust automated test scripts using Katalon Studio (Web and API).</li>
<li>Collaborate with developers, business analysts, and manual QA engineers to define clear acceptance criteria and test scenarios.</li>
<li>Perform API testing using tools like Katalon, Postman, and Seleniuim.</li>
<li>Analyze test results, identify root causes of issues, and provide detailed reports on defects and test coverage.</li>
<li>Continuously enhance automation frameworks for scalability and maintainability.</li>
<li>Contribute to test planning, estimation, and documentation of test strategies and approaches.</li>
<li>Participate in Agile/Scrum ceremonies &mdash; sprint planning, retrospectives, and daily standups.</li>
<li>Mentor junior QA engineers and promote automation best practices.</li>
</ul>
Requirements:
<ul><li>Bachelor&rsquo;s degree in Computer Science, Information Technology, Engineering, or related field.</li>
<li>5+ years of overall experience in Software Testing, with at least 3+ years in test automation.</li>
<li>Strong hands-on experience in Katalon Studio (Web UI, API, Mobile).</li>
<li>Proficiency in Groovy/Java scripting for test automation.</li>
<li>Experience with version control systems (e.g., Git, Bitbucket).</li>
<li>Familiarity with CI/CD tools (Jenkins, GitHub Actions, Bamboo, etc.).</li>
<li>Experience working in Agile/Scrum development environments.</li>
<li>Strong understanding of SDLC, STLC, and defect lifecycle management.</li>
<li>Working knowledge of test management tools (e.g., Jira, Zephyr, TestRail).</li>
<li>Excellent problem-solving and analytical skills.</li>
<li>Strong communication and collaboration abilities.</li>
</ul>
Preferred / Nice-to-Have Skills:
<ul><li>Exposure to Appium, or other automation frameworks.</li>
<li>Experience with BDD frameworks (Cucumber, Gherkin).</li>
<li>Basic knowledge of SQL for database validation.</li>
<li>API automation experience beyond Katalon (e.g., RestAssured, Karate).</li>
</ul>
We have an amazing team of 700+ individuals working on highly innovative enterprise projects &amp; products. Our customer base includes Fortune 100 retail and CPG companies, leading store chains, fast-growth fintech, and multiple Silicon Valley startups.
What makes Confiz stand out is our focus on processes and culture. Confiz is ISO 9001:2015 (QMS), ISO 27001:2022 (ISMS), ISO 20000-1:2018 (ITSM), ISO 14001:2015 (EMS), ISO 45001:2018 (OHSMS) Certified. We have a vibrant culture of learning via collaboration and making workplace fun.
People who work with us work with cutting-edge technologies while contributing success to the company as well as to themselves.
To know more about Confiz Limited, visit: https://www.linkedin.com/company/confiz-pakistan/</div>

QA Automation Engineer (Katalon)

<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

<div>We are seeking an experienced engineer to design and implement a Quality Assurance (QA) framework for automated testing across our cloud-native, real-time, and batch data pipelines. The ideal candidate will have deep expertise in Python-based test frameworks, data validation at scale, and CI/CD integration, ensuring reliability, accuracy, and performance in our data platform.
Key Responsibilities
<ul><li>Design and develop a scalable automated data quality and testing framework for real-time (Kafka/Flink/Spark Streaming) and batch (PySpark) data pipelines.</li>
<li>Integrate automated data validation (schema checks, statistical profiling, anomaly detection) into data workflows using tools like Great Expectations, Deequ, or custom-built Python solutions.</li>
<li>Build test harnesses and reusable libraries for unit, integration, and regression testing of ETL pipelines and APIs.</li>
<li>Implement continuous testing pipelines integrated with CI/CD tools (Azure DevOps, GitHub Actions, or Jenkins).</li>
<li>Collaborate with data engineers to embed data quality gates within orchestration tools (Azure Data Factory / Airflow).</li>
<li>Define and monitor data quality KPIs, thresholds, and alerting using observability tools (Datadog, Prometheus, etc.).</li>
<li>Develop mock data generation and simulation frameworks for performance and stress testing.</li>
<li>Ensure comprehensive test coverage for schema evolution, transformation logic, and downstream data consumption APIs.</li>
<li>Contribute to best practices and documentation around test-driven data engineering and quality-first development culture</li>
<li>Have experience of Shift-Left Testing and Test-Driven Data Engineering</li>
<li>Integrate QA Framework with Orchestration and Monitoring Pipelines</li>
<li>Develop Synthetic Data Generators for Edge Cases and Negative Testing</li>
<li>Validate Schema Evolution and Backward Compatibility</li>
<li>Optimize Testing for Cost Efficiency</li>
<li>Ensure Stability of Every Release</li>
</ul>
Required Skills
<ul><li>Strong knowledge of data warehousing, lakehouse architectures, and data lake</li>
<li>Overall 6+ years of experience in data warehousing domain and 3+ in ETL testing and data quality</li>
<li>Strong Python development skills, emphasizing modular, testable, and reusable code.</li>
<li>Hands on knowledge of test automation tools and libraries for data warehouse solutions.</li>
<li>Expertise with data quality libraries such as Great Expectations, Deequ, Soda Core, or equivalent.</li>
<li>Solid understanding of SQL and ability to validate transformations over large-scale datasets.</li>
<li>Familiarity with Apache Spark (PySpark) and real-time data processing frameworks (Kafka, Flink, Spark Streaming).</li>
<li>Experience with Azure ecosystem (Data Factory, Databricks, Storage, Synapse).</li>
<li>Experience with CI/CD pipelines and automated testing workflows.</li>
<li>Exposure to monitoring and alerting for data quality metrics</li>
</ul>
We have an amazing team of 700+ individuals working on highly innovative enterprise projects &amp; products. Our customer base includes Fortune 100 retail and CPG companies, leading store chains, fast-growth fintech, and multiple Silicon Valley startups.
What makes Confiz stand out is our focus on processes and culture. Confiz is ISO 9001:2015 (QMS), ISO 27001:2022 (ISMS), ISO 20000-1:2018 (ITSM), ISO 14001:2015 (EMS), ISO 45001:2018 (OHSMS) Certified. We have a vibrant culture of learning via collaboration and making workplace fun.
People who work with us work with cutting-edge technologies while contributing success to the company as well as to themselves.
To know more about Confiz Limited, visit: https://www.linkedin.com/company/confiz-pakistan/</div>

Data Quality & Test Automation Framework Engineer

<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

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