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<p>Process Improvement Specialist - Lean Six Sigma Certified</p><p>Process Excellence (PEx) Black Belt Leader is responsible for being a change agent, leading improvement teams and working projects focused - Early Development as part of the PEx team.  During this full-time assignment, PEx consultants are expected to complete the following:  Lead and complete black belt projects within Early Development both locally and globally, coach and mentor business departments leaders, including green belt candidates and provide training to broaden the culture of process excellence within the business unit.</p><p><b>Duties and Responsibilities:</b></p><ul><li>Leads process improvement teams and directs timely completion of projects that support critical goals and customer satisfaction requirements and serves as the departmental point of contact for specific project initiatives and best practices.</li><li>Assists process owners, project champions, and business unit leaders to facilitate setting priorities, developing agendas and designing objectives related to Labcorp Drug Development Process Excellence.</li><li>Train, mentor, coach and challenge others in the use of statistical tools and Process Excellence approaches and techniques to establish a process acumen mindset at the department or process level.</li><li>Demonstrates Project Management techniques on existing projects by managing multiple priorities effectively and meeting commitments in an accurate and timely manner.</li><li>Identify and present opportunities to business leaders and champions to improve customer satisfaction, increase net income, enhance productivity and further employee performance across business units within the Early Development business.</li><li>Identifies and shares leveraging opportunities or best practices across business units within the Early Development business.</li><li>Support ED project management and process excellence efforts with other duties as assigned.</li></ul><p><b>Education / Qualifications:</b></p><ul><li>Six Sigma Black Belt certification preferred, Six Sigma Green Belt will be considered.</li><li>BSc/BA is required; relevant experience may be substituted for education.</li><li>Engineering degree or other technical background preferred.</li></ul><p><b>Experience</b>:</p><ul><li>7+ years in Process <span>Excellence/Improvement</span> roles</li><li>Direct experience working in a global matrix organization.</li><li>Project Management skills, including an ability to plan and execute projects and meet commitments in an accurate and timely manner.</li><li>Strong facilitations skills as demonstrated with various levels in an organization.</li><li>Strong technical skills as applied to obtaining and analyzing business metrics</li><li>Strong leadership and communication skills to senior leadership at the executive level and above.</li><li>Pharmaceuticals or Drug Development regulatory (GLP) experience highly preferred but not essential</li></ul><p><b>Labcorp is proud to be an Equal Opportunity Employer:</b></p><p>Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. A<span>dditionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. </span></p><p><b>We encourage all to apply</b></p><p>If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our <a href="https://careers.labcorp.com/global/en/accessibility" rel="noopener noreferrer" target="_blank">accessibility site</a> or contact us at <a href="mailto:Disability_apply@LabCorp.com" rel="noopener noreferrer" target="_blank">Labcorp Accessibility.</a> For more information about how we collect and store your personal data, please see our <a href="https://www.labcorp.com/about/web-privacy-policy" rel="noopener noreferrer" target="_blank">Privacy Statement</a>.</p><h4>Experience Level</h4>Senior Level

LabCorp

Process Analyst

<p>Assoc Dir Global Quality Function - 3544</p><h4><b>Who we are</b></h4>
Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.<h4><b>The opportunity</b></h4><ul><li>Ensures that the Product Quality Reviews / Annual Product Reviews for Teva products are completed in a timely and compliant manner as per Teva’s CORP Quality Management systems. PQR/APR compilation and approval must be well associated with the Teva Manufacturing Sites, Global Quality Units and Commercial affiliates to meet the targets and ensure compliance.</li><li>Ensures timely and accurate data migration in collaboration with sites and Global IT / IT Quality</li><li>Ensures timely review of CMC documentation in collaboration with Global R&amp;D sites</li><li>Defines team operating standards and ensures essential CORP and local procedures are followed based on knowledge of own discipline.</li><li>Manages and supervises a team of up to 100 professional employees consisting of sr. managers, managers, authors reviewers and approvers.</li><li>Is accountable for the performance and results of a teams within the function Global Quality GBS.</li><li>Creates and adapts departmental plans and priorities to address resource and operational challenges.</li><li>Ensures that decisions are guided by CORP policies, procedures and Global Quality´s business plan.</li><li>Receives guidance from Senior Director Quality Strategy and Shared Services, SVP Global Quality, other Managers in Quality Strategy and Shared Services, Global R&amp;D, Global IT, EMSO Quality affiliates, Commercial Quality EU &amp; IM, TGO sites.</li></ul><h4><b>How you’ll spend your day</b></h4><p>A.Review and approval of PQR’s</p><p>The owner of the function</p><p>• Review of  Annual Product Reviews (APRs) / Product Quality Reviews (PQRs) for products supplied by external vendors and manufactured at external manufactures<br/>• Conduct review of (APRs) / Product Quality Reviews (PQRs) prepared by team members to ensure high quality of the reports prepared by the team.<br/>• Recommend actions and communicate to stakeholder   for identified actions as part of the review process to  improve quality of products(CAPA)<br/>• Approve Annual Product Reviews (APRs) / Product Quality Reviews (PQRs) which do not require approval step by any other TEVA /non-TEVA stakeholder like QPs, RPs or FvPs.<br/>• Support and guide in escalation of PQR issues and initiate and conduct meetings / telecons if required on priority.<br/>• Escalate the issues of the team to higher management for non-responsive CMO’s and TEVA’s internal stake holders</p><p>B.Data Migration</p><p>• Ensure Data Migration is performed in accordance with TEVA requirements in the pre-given timeline and accuracy<br/>• Support and guide in escalation of DM issues and initiate and conduct meetings / telecons if required on priority.<br/>• Escalate the issues of the DM team to higher management for non-responsive TEVA’s internal stake holders, missing resources, missing commitments etc.</p><p>C.R&amp;D CMC Documentation<br/>• Ensure review of CMC documents received from R&amp;Ds is performed in accordance with TEVA requirements in the pre-given timeline and accuracy<br/>• Support and guide in escalation of issues and initiate and conduct meetings / telecons if required on priority.<br/>• Escalate the issues to higher management for non-responsive TEVA’s internal stake holders, missing resources, missing commitments etc.</p><p>D.Quality Management Systems</p><p>The owner of the function</p><p>• Ensures that the local quality management system is maintained at GBS Quality function.<br/>• Ensures that the local Quality Management System is compliant with respective regulatory guidelines and TEVA´s CORP QMS (Gap Assessments)<br/>• Approves process of change controls and deviations<br/>• Approves local SOP’s and its related documents.<br/><br/></p><p>E.Performance Management</p><p>• Monitors and compiles the KPI scores of the various business units and supports the team to improve their efficiency. <br/>• Participates in the customers council meetings and supports the effectiveness of the councils.<br/>• Leads or participates in the Monthly Quality Council and enhances the effectiveness and efficiency of it by suitable reports/metrices and continuous improvement.<br/><br/></p><p>F.Training</p><p>The incumbent </p><p>• Approves Training Materials for GMP training and on the job training.<br/>• Imparts training on procedures as needed. <br/>• Reviews the training status of the team and regularly verifies that training was performed in time and successfully. <br/>• Certifies trainers and self-inspectors to enable them to impart training and conduct self-inspection.</p><p><br/>G.Miscellaneous Support</p><p>The owner of the function is responsible for</p><p>• Hiring of new Headcount and monitoring the Head count status <br/>• Maintaining Employee Central and other relevant Master Data<br/>• Liase with Finance related to the HC cost<br/>• Responsible for approval of PR’s related to purchase of PQR’s.<br/>• Review the invoicing cost involved with respect to the status.<br/>• Approval of POs in SAP- for hiring and other requests like purchase orders for costs involved in updation of software <br/>• Review monthly report to be presented to higher management<br/><br/></p><h4><b>Your experience and qualifications</b></h4><p>• More than 15 years of experience in QA / QC function in the pharmaceutical industry<br/>• More than 5 years of experience in a managerial role<br/>• Well-founded knowledge on worldwide cGxP regulations<br/>• Excellent English language skills, other language skills could be helpful<br/>• Very Good communication skills and ability to work in a matrix structure<br/>• Very good knowledge of Computerised Systems in TEVA´s IT landscape (Track-Wise, SAP, LIMS, Global Insights, Glorya etc.)<br/>• Good understanding of manufacturing, QC and Contract manufacturing processes<br/>• Engagement to drive improvements and ability to manage complexity<br/>• Mobility</p><h4><b>Reports To</b></h4><p>VP Global Quality SMSO</p><h4><b>Already Working @TEVA?</b></h4><p>If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: <a href="https://performancemanager.successfactors.eu/sf/careers/jobsearch?bplte_company=1080030P"> Internal Career Site </a></p><p>The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.</p><h4><b>Teva’s Equal Employment Opportunity Commitment</b></h4>
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to  support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.<h4>Experience Level</h4>Senior Level

Teva Pharmaceuticals

Chief Quality Officer

<p>Trainee - Testing</p><h4><b>About SLK</b></h4><p>SLK is a global technology services provider focused on bringing AI, intelligent automation, and analytics together to create leading-edge technology solutions for our customers through a culture of partnership, led by an evolutionary mindset. For over 20 years, we've helped organizations across diverse industries - insurance providers, financial service organizations, investment management companies, and manufacturers - reimagine their business and solve their present and future needs.</p><p> </p><p>At SLK, we champion diversity and inclusion, valuing the unique perspectives and talents each individual brings. We empower specially abled talent by fostering a supportive environment that welcomes every member's abilities. Our goal is to create an innovative workspace enriched by diversity, providing reasonable accommodations to ensure everyone can contribute to our success. We invite candidates from diverse backgrounds to help us build a more inclusive future.</p><h4><b>BASIC INFORMATION ON THE POSITION</b></h4><p> </p><p>Position Name: Trainee - Testing</p><p> </p><h4><b>Mandatory/Required Skills &amp; Location</b></h4><p>Location:</p><p>Mandatory/Required Skills:</p><h4><b>PURPOSE OF THE ROLE</b></h4><p> </p><p>This role is responsible for understanding functional requirements, test cases &amp; execute test cases, log &amp; retest defects. Overall responsible for testing the application modules assigned and ensure quality test deliverables.</p><h4><b>KEY RESPONSIBILITIES AND ACCOUNTABILITIES</b></h4><p> </p><ul><li>Understand the application functionalities &amp; requirements</li><li>Understand Test Scenarios, Test cases &amp; request Test Data as needed</li><li>Execute Test cases, log &amp; retest defects. Report testing status</li><li>Adhere to SLK and Project related processes, Security guidelines, process related activities etc</li><li>Participate in all the L&amp;D mandatory trainings of 6 days minimum per year.</li></ul><h4><b>EDUCATION QUALIFICATION</b></h4><p> </p><ol><li>BE/B.Tech/ME/M.Tech/MCA/MSc</li><li>Trained in Testing (preferably)</li></ol><h4><b>MINIMUM EXPERIENCE REQUIRED</b></h4><p> </p><ol><li>None. </li><li>Trained in Testing (preferably)</li></ol><h4><b>DOMAIN/ FUNCTIONAL SKILLS</b></h4><p> </p><ul><li>Testing Principles, HP QC knowledge is desirable.</li></ul><h4>Experience Level</h4>Entry Level

SLK Software Private Limited

Quality Assurance Intern

<p>Engineer, Quality Global Process Owner (GPO) for Audits</p><p><b>Job Title: Engineer, Quality Global Process Owner (GPO) for Audits</b></p><p><b><span>About <span><span>GlobalFoundries </span></span></span></b></p><p>GlobalFoundries is a leading full-service semiconductor foundry providing a <span><span>unique combination</span></span> of design, development, and fabrication services to some of the world’s most inspired technology companies. With a global manufacturing footprint spanning three continents, GlobalFoundries makes possible the technologies and systems that transform industries and give customers the power to shape their markets. For more information, visit <a href="http://www.gf.com/" rel="noopener noreferrer" target="_blank"><span>www.gf.com</span></a>. </p><p><b>Summary of Role</b></p><p>We are looking for a Global Process Owner (GPO) for Audits to join our team as part of the global QMS (Quality Management System). The successful candidate will be responsible to strategize, develop, implement, monitor, and improve Audit related business process across the organization</p><p>This position is based at our GlobalFoundries office at Bengaluru, India.</p><p><b>Responsibilities include:</b></p><ul><li>Own and manage Audits business processes across the company for both internal and external audits</li><li>Ensure consistent execution of the process across all business functions and geographies</li><li>Incorporate quality methods and best practices into the identified areas of improvement to enhance the overall quality, speed, and cost of operations.</li><li>Proactively work with stakeholders and push to identify and agree on continuous improvement plans.</li><li>Learn, develop, and execute quality assurance plans and strategies to ensure consistent adherence to quality standards</li><li>Maintain and monitor changes to various international quality specifications</li><li>Manage corporate memberships &amp; subscriptions for quality specifications</li><li>Analyze data to identify trends and opportunities for improvement, and work with business functions to implement corrective actions.</li><li>Develop and deliver training programs to build a culture of quality and continuous improvement across the organization.</li><li>Collaborate with cross-functional teams to ensure alignment of quality assurance initiatives with overall business objectives, meet compliance requirements and drive towards process excellence</li><li>Act as a subject matter expert and advisor on quality assurance matters to business functions and senior management</li><li>Develop next-generation Audit software using SAP-QM</li><li>Collaborate and communicate process changes to stakeholders and leadership</li></ul><p><b>Required qualifications:</b></p><ul><li>Bachelor’s degree in engineering or science is preferred; Masters/PhD from a top ranked university is a plus</li><li>5-10 years of work experience in quality assurance, process improvement, or related field</li><li>Certified ISO/IATF/VDA Auditor with proven working experience as Auditor</li><li>Fast learner, strong analytical and problem-solving skills, with the ability to analyze data and identify trends and opportunities for improvement.</li><li>Excellent communication and interpersonal skills, with the ability to build strong relationships with business functions and stakeholders.</li></ul><ul><li>Self-starter with the ability to work independently and as part of a team</li><li>Language Fluency – English (Written &amp; Verbal)</li><li>This position requires global time-zone coverage and hence you may have to start the work late in the day, from 10AM to 8PM IST</li></ul><p><b>Additional preferred qualifications:</b></p><ul><li>Hands on experience on problem <span>solving/troubleshooting</span> skills</li><li>Working knowledge of <span>ISO9001:2015/IATF16949</span></li><li>Work experience with multi-national and cross functional environments</li><li>Possess the right attitude to get results with a Growth Mindset</li></ul><p>If you are a results-driven individual with a passion for process excellence, we encourage you to apply for this exciting opportunity to join our team as an Audits Global Process Owner.</p><p>GlobalFoundries is an equal opportunity employer, cultivating a diverse and inclusive workforce. We believe having a multicultural workplace enhances productivity, efficiency, and innovation whilst our employees feel truly respected, valued and heard.   </p><p>As an affirmative employer, all qualified applicants are considered for employment regardless of age, ethnicity, marital status, citizenship, race, religion, political affiliation, gender, sexual orientation and medical and/or physical abilities. All offers of employment with GlobalFoundries are conditioned upon the successful completion of background checks, medical screenings as applicable and subject to the respective local laws and regulations.  </p><p>To ensure that we maintain a safe and healthy workplace for our GlobalFoundries employees, please note that offered candidates who have applied for jobs in India will have to be fully vaccinated prior to their targeted start date. For new hires, the appointment is contingent upon the provision of a copy of their COVID-19 vaccination document, subject to any written request for medical or religious accommodation.</p><p><span>Information about our benefits you can find here: <a href="https://gf.com/about-us/careers/opportunities-asia" rel="noopener noreferrer" target="_blank"><span>https://gf.com/about-us/careers/opportunities-asia</span></a></span></p><p><span> </span></p><h4>Experience Level</h4>Senior Level

Globalfoundries Engineering Private Limited

<p>Manager- Quality (DDRC)</p><div>
  
</div><div><p>Business: Piramal Pharma Solutions<br/>Department: Quality<br/>Location: Kurla<br/>Travel: Low</p><div><br/></div></div><div><strong>Job Overview: </strong><span>Remote support to PPL sites in reviewing analytical data remotely, preparing master build in LIMS (Lab Vantage / Labware), Document Preparation (specifications, test methods, protocols, etc.) and uploading for review in ensure, initiating QMS elements in Trackwise / eDMS.</span><br/></div><div><div><br/></div><div><strong>Key Stakeholders: Internal</strong></div><div><span>Site Quality Team (QC, QA), Corporate Functions      </span></div><div>
      
 </div><div><br/></div><div><strong>Key Stakeholders: External </strong></div><div><span>Regulators (during inspection), Solution Providers</span></div><div><br/></div><div><strong>Reporting Structure</strong></div><div><br/><span>PPL Site Quality (Functionally) and CQA Document, Data Review &amp; Creation (Administratively)</span></div><div>
   
 </div><p><strong>Qualification</strong></p><p><span>B. Pharm / M. Pharm / M.Sc. Chemistry / B.Sc. Chemistry or equivalent/Microbiology</span></p><div><br/></div><div><strong>Experience</strong></div><div><span>•</span><span>Need to be ready to live and embrace the Piramal values.</span></div><div><span>•</span><span>Quality professional with 8+ years of QC / QA experience in a regulated pharma companies. </span></div><div><span>•</span><span>Must have hands-on experience in Laboratory software's, testing, applications and systems (Chromatography By HPLC and GC, UV, IR, Dissolution, Malvern, KF auto titrator, etc).</span></div><div><span>•</span><span>Must have worked in LIMS for Data entry  / master build, and data review.</span></div><div><span>•</span><span>Knowledge of applicable regulatory requirements / regulations (USFDA, EU, Health Canada, others).</span></div><div><span>•</span><span>Need to be aware of latest regulations and pharmacopeial requirements.</span></div><div><span>•</span><span>Well-organized and committed, with strong verbal and written communication skills. Good Collaboration skills and Team player.</span><br/></div><div><br/></div><div><strong>Key Roles and Responsibilities:</strong></div><div><span>•</span><span>Preparation of Master Build in LIMS.</span></div><div><span>•</span><span>Oversee track-wise operations for QMS activities.</span></div><div><span>•</span><span>Preparation and review of Method Validation, Method Transfer, Method Verification, and Equivalency documents.</span></div><div><span>•</span><span>Preparation and review of Test Methods, STPs, and Specifications.</span></div><div><span>•</span><span>Operational knowledge of eDMS and ensure application compliance.</span></div><div><span>•</span><span>Monitor compendial changes and prepare evaluation reports (including specifications and methods) for affected site products and materials.</span></div><div><span>•</span><span>Review analytical data, raw data, chromatography, and LIMS for RM/PM/FP.</span></div><div><span>•</span><span>Prepare and review new SOPs.</span></div><div><span>•</span><span>Ensure timely completion of documentation.</span></div><div><span>•</span><span>Maintain data integrity while preparing, uploading, or reviewing documents.</span></div><div><span>•</span><span>Collaborate effectively across Piramal Plants.</span></div><div><span>•</span><span>Provide support to any PPL site as required, with role assignments based on evolving needs and timelines.</span></div><div><span>•</span><span>Perform activities across US, Canada, and EU time zones; available to travel for up to 3 months to PPL sites (India and overseas) as needed.</span></div><p><span>Perform additional tasks as assigned by the Leadership team based on requirements</span></p></div>

Piramal Pharma

Quality Manager

<p>Deputy Manager - Transactional Quality - Hyd - REF62792M (Transactional Quality, Transformational Quality experience)</p><h4>Company Description</h4><p>WNS (Holdings) Limited (NYSE: WNS), is a leading Business Process Management (BPM) company. We combine our deep industry knowledge with technology and analytics expertise to co-create innovative, digital-led transformational solutions with clients across 10 industries. We enable businesses in Travel, Insurance, Banking and Financial Services, Manufacturing, Retail and Consumer Packaged Goods, Shipping and Logistics, Healthcare, and Utilities to re-imagine their digital future and transform their outcomes with operational excellence.We deliver an entire spectrum of BPM services in finance and accounting, procurement, customer interaction services and human resources leveraging collaborative models that are tailored to address the unique business challenges of each client. We co-create and execute the future vision of 400+ clients with the help of our 44,000+ employees.</p><h4>Job Description</h4><p>Quality Manager Job Description Quality Manager oversees quality assurance processes and ensure compliance with industry standards and regulations. The ideal candidate will develop, implement, and maintain quality control systems to enhance product reliability and customer satisfaction. Spearhead Continuous Improvement Process.</p><p>Key Responsibilities:</p><p>• Develop and enforce quality control policies and procedures.<br/>• Monitor and analyze quality performance metrics.<br/>• Conduct audits, inspections, and risk assessments.<br/>• Ensure compliance with regulatory and industry standards.<br/>• Investigate quality issues and implement corrective actions.<br/>• Collaborate with Operations and other department to enhance quality.</p><h4>Qualifications</h4><p>1. Educational Background<br/>• Bachelor’s Degree: o Engineering (Mechanical, Industrial, Electrical) Business Administration Manufacturing Quality Assurance or other related fields</p><p>2. Work Experience<br/>• Relevant Quality Management Experience<br/>• Leadership Experience: This includes supervising teams, managing quality improvement initiatives, and liaising with other departments.<br/>• Familiarity with Shipping and Logistics cycle is a plus.</p><p>3. Skills and Knowledge<br/>• Strong Knowledge of Quality Management Systems (QMS): Familiarity with industry standards and methodologies (ISO 9001, Lean, Six Sigma, etc.) is critical.<br/>• Analytical Skills: Ability to analyze data, identify trends, and make data-driven decisions.<br/>• Problem-Solving Skills: Resolving issues related to product quality and finding solutions to prevent them in the future.<br/>• Communication Skills: Ability to communicate clearly with internal teams and external stakeholders, especially when explaining quality requirements or presenting reports.<br/>• Attention to Detail: Ensuring products or services meet the required standards and identifying issues before they become problems.<br/>• Project Management: Ability to lead and manage quality improvement projects effectively.</p><p>4. Continuous Improvement Mindset<br/>• Experience in running ideation sessions and leading process improvement projects within the organization with significant benefits.• Familiarity in Process Improvement Methodologies.<br/>• Knowledge and familiarity with automation principles and methodologies.</p><h4>Experience Level</h4>Mid Level

WNS Global Services Pvt Ltd

<p>Quality Analyst</p><p>Join us as a Quality Automation Specialist</p><ul><li>In this key role, you’ll be undertaking and enabling automated testing activities in all delivery models</li><li>We’ll look to you to support teams to develop quality solutions and enable continuous integration and assurance of defect free deployment of customer value</li><li>You’ll be working closely with feature teams and a variety of stakeholders, giving you great exposure to professional development opportunities</li><li><p>We're offering this role at associate level</p></li></ul><h4>What you'll do</h4><p>Joining us in a highly collaborative role, you’ll be contributing to the transformation of testing using quality processes, tools, and methodologies, significantly improving control, accuracy and integrity. You’ll make sure repeatable, constant and consistent quality is built into all phases of the idea to value lifecycle at reduced cost or reduced time to market. It’s a chance to work with colleagues at multiple levels, and with cross-domain, domain, platform and feature teams, to build in quality as an integral part of all activities.</p><p>Additionally, you’ll be:</p><ul><li>Supporting the design of automation test strategies, aligned to business or programme goals</li><li>Actioning and evolving more predictive and intelligent testing approaches, based on automation and innovative testing products and solutions</li><li>Collaborating to refine the scope of manual and automated testing required, the creation of automated test scripts, user documentation and artefacts</li><li>Designing and creating a low maintenance suite of stable, re-usable automated tests, which are usable both within the product or domain and across domains and systems in an end-to-end capacity</li><li>Applying testing and delivery standards by understanding the product development lifecycle along with mandatory, regulatory and compliance requirements</li></ul><h4>The skills you'll need</h4><p>We’re looking for someone with experience of automated testing, particularly from an Agile development or CI/CD environment. You’ll be an innovative thinker who can identify opportunities and design solutions, coupled with the ability to develop complex automation code.</p><p>You’ll have a good understanding of Agile methodologies with experience of working in an Agile team, with the ability to relate everyday work to the strategic vision of the feature.</p><p>We’ll also look for you to have:</p><ul><li>Four to seven years of experience in end-to-end, UI and API non-functional testing using the latest tools as recommended by the enterprise tooling framework such as JMeter, LoadRunner</li><li>Strong background of designing, developing and implementing non-functional tests sucha s load, soak, stress in AWS environments using Java, JavaScript scripting languages and analysing these tests</li><li>Excellent communication skills with the ability to simplify complex technical concepts to management level colleagues</li><li>Strong collaboration and stakeholder management skills, producing detailed reports to align with banking governance</li></ul><p>Hours</p>45<p><u><b>Job Posting Closing Date:</b></u></p>15/09/2025

NatWest Group

Quality Analyst

<p>Team Member - Analytical Quality Assurance</p><h4>Company Description</h4><p>Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because <strong>Good Health Can’t Wait</strong>.</p><p>We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. </p><p>For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).</p><p>‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable.  Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency</p><p>Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.</p><h4>Job Description</h4><p><strong>Job Summary</strong><br/><strong>Roles &amp; Responsibilities</strong><br/></p><ul><li>Review and approval of all analytical test data of Quality control.</li><li>Review and usage decision of analytical reports in LIMS, Empower and SAP.</li><li>Electronic signatures level-2 for chromatography data station (CDS) and standalone instruments.</li><li>Review the Analytical test report in LIMS.</li><li>Review the reported results against specification and trends.</li><li>Review the method validation and method transfer documents.</li><li>Review the instrument calibrations and working standard qualification records.</li><li>Handling the Incidents/ Deviations, Out of Trends, Out of Specification including investigations, Corrective and Preventive actions follow up and closure.</li><li>Monitoring of analytical activities in Quality control laboratory.</li><li>Verification of Specifications/standard test Procedures/Worksheets/Analytical Reports before Approval.</li><li>Verification and review of the audit trails for Standalone, Empower and LIMS.</li><li>Ensure cGMP / cGLP compliance.</li><li>To follow Safety, Health and Environmental procedures and practices.</li><li>Review and approval of excel sheet validations.</li><li>Review results acceptance for API and Excipients and Packing material.</li><li>Review of compiled of Stability Data and its verification/ Exhibit batch sampling protocols.</li><li>Handling of Robotic Process Automation of Chromatography Data review (RPACD)</li><li>To carry any other activities assigned by upward reporting staff.</li></ul><h4>Qualifications</h4><p><strong>Educational qualification: </strong>A Bachelor’s/Master's degree in Pharmacy, Chemistry, Chemical Engineering, or a related field<br/><br/><strong>Minimum work experience</strong>: 3 to 7 years of experience in QC or AQA department is mandatory.<br/><br/><br/></p><h4>Additional Information</h4><p><strong>About the Department<br/>Global Manufacturing Organisation (GMO)</strong><br/>At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry.<br/>We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities.<br/>Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future.<br/><br/><br/><strong>Benefits Offered</strong><br/>At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs.<br/>The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining &amp; relocation support, family support (Maternity &amp; Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.<br/><br/><strong>Our Work Culture</strong><br/>Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.<br/>For more details, please visit our career website at <strong>https://careers.drreddys.com/#!/ </strong></p><h4>Experience Level</h4>Entry Level

Dr Reddys Laboratories

Quality Assurance Associate

<p>Technical Auditor</p><p><br></p><p><strong>Eligibility:</strong></p><ul><li><a rel="noopener noreferrer" href="\&quot;http://b.tech/B.E\&quot;" target="_blank">B.Tech/B.E</a>. (Food Tech, Dairy Tech, Biotech, Chemical, Textile &amp; Fibre, Agri, Petrochemical) OR <a rel="noopener noreferrer" href="\&quot;http://m.sc/\&quot;" target="_blank">M.Sc</a>. (Chemistry, Biochemistry, Microbiology)</li><li>Minimum 60% marks / 6.0 CGPA / First Division</li><li>2–5 years of relevant experience (Graduated before Feb 2023)</li></ul><p><br></p><p><strong> Role Highlights:</strong></p><ul><li>Conduct on-site factory inspections under BIS standards</li><li>Assess processes, raw materials &amp; lab facilities</li><li>Ensure compliance across Food, Chemical &amp; Textile sectors</li></ul><p><br></p><p>Share your resume now.</p>

Quality Austria Central Asia

External Auditor

<p>Quality Engineer (Tester)</p><b>Project Role : </b>Quality Engineer (Tester)<br/><b>Project Role Description : </b>Enables full stack solutions through multi-disciplinary team planning and ecosystem integration to accelerate delivery and drive quality across the application lifecycle. Performs continuous testing for security, API, and regression suite. Creates automation strategy, automated scripts and supports data and environment configuration. Participates in code reviews, monitors, and reports defects to support continuous improvement activities for the end-to-end testing process.                                                 <br/><b>Must have skills : </b>Test Management<br/><b>Good to have skills : </b>NA<br/>Minimum <b>3</b> year(s) of experience is required<br/><b>Educational Qualification : </b>15 years full time education<br/><br/>Summary: 
As a Quality Engineer, you will enable full stack solutions through multi-disciplinary team planning and ecosystem integration to accelerate delivery and drive quality across the application lifecycle. Your typical day will involve performing continuous testing for security, API, and regression suites, creating automation strategies, and supporting data and environment configurations. You will also participate in code reviews, monitor and report defects, and engage in continuous improvement activities for the end-to-end testing process, ensuring that quality is maintained throughout the development lifecycle.
 
Roles &amp; Responsibilities: 
- Expected to perform independently and become an SME.
- Required active participation/contribution in team discussions.
- Contribute in providing solutions to work related problems.
- Collaborate with cross-functional teams to ensure alignment on project goals and quality standards.
- Develop and maintain comprehensive test plans and test cases to ensure thorough coverage of application features.
 
Professional &amp; Technical Skills: 
- Must To Have Skills: Proficiency in Test Management, Risk Management.
- Strong understanding of automated testing frameworks and tools.
- Experience with continuous integration and continuous deployment practices.
- Ability to analyze and interpret complex data sets to inform testing strategies.
- Familiarity with various programming languages and scripting for test automation.
 
Additional Information: 
- The candidate should have minimum 3 years of experience in Test Management.
- This position is based at our Bengaluru office.
- A 15 years full time education is required.

Accenture India Private Limited

Quality Engineer

<p>Q.A OFFICER</p><h4>Job Purpose and Impact</h4><p>The Food Safety Quality Technician III will complete a variety of monitoring and verification tasks to ensure that the plant operates in compliance with food safety programs, policies and certifications. In this role, you will influence people who are not direct reports to achieve overall quality standards and meet governmental agency quality standards.</p><h4>Key Accountabilities</h4><ul type="disc"><li>Complete food safety, sanitation, operational, risk material and control room monitoring.</li><li>Review daily material processing procedures and verify all applicable monitoring documents, taking immediate corrective actions when deviations are identified.</li><li>Maintain quality records, imputing and assigning deviation reports as required.</li><li>Conduct daily inspections of the plant for each one of the critical control points and sanitation monitoring zones, ensuring all monitors are adhering to the written food safety programs.</li><li>Perform unbiased audits throughout the facility to ensure adherence to sanitation procedures for critical job tasks.</li><li>Communicate deviations to management and ensure they are documented, assigned correctly and completed in a timely manner and follow up on corrective actions and preventative measures to ensure they are effective.</li><li>Provide and administer food safety and quality certification training to plant employees including theoretical training related to quality programs.</li><li>Handle complex clerical, administrative, technical or customer support issues under minimal supervision, while escalating only the most complex issues to appropriate staff.</li><li>Other duties as assigned</li></ul><h4>Qualifications</h4><h4>Minimum Qualifications</h4><ul type="disc"><li>Degree in chemistry or bachelor’s in pharmacy level or equivalent</li><li>Experience with email, spreadsheet and word processing applications</li><li>Knowledge of food safety concepts, including hazard management and governmental agency requirements</li><li>Able to represent the company during third party audits and governmental agency verifications</li></ul><h4>Preferred Qualifications</h4><ul type="disc"><li>Bachelor's degree in a science related field</li><li>Minimum of two to three years of experience in a bulk drug manufacturing facility</li><li>Experience or knowledge of QMS, GMP, GDP, Data integrity and QRM Documentation. </li></ul><h4>Experience Level</h4>Senior Level

Cargill India

Quality Assurance Officer

<p>Executive</p><p>Candidate shall have detailed knowledge on equipment qualification, computer system validation</p><p>Review of the Equipment Qualification Protocols and Final reports and Monitoring of the Equipment Qualification like IQ, OQ and PQ. Review of Qualification documents for IQ, OQ and PQ done by the Vendor/Third party related to Instrument integrated with equipment.</p><p>Experience in handling of QMS related activities: Change control, Deviation, CAPA.</p><h4>Experience Level</h4>Executive Level

lupin ltd

Quality Technician

<p>QMS/CAPA Engineer</p><h4>Job Title</h4>QMS/CAPA Engineer<h4>Job Description</h4><p><b>Job title:</b><br/><b><span>QMS/CAPA Engineer </span></b></p><p><span>Responsible for supervising the QMS team, ensuring efficient execution of quality management system (QMS) activities in compliance with company policies. The role monitors key quality performance indicators, analyzing data to identify trends and areas for improvement, and reporting to higher management. The role ensures timely process implementation and deployment, tracking progress and verifying effectiveness. The role conducts risk assessments and manages mitigation activities, developing strategies to minimize impact and facilitates cross-functional collaboration to resolve quality issues. The role drives continuous improvement initiatives within the QMS, proposing enhancements to processes, tools, and systems, guiding the QMS team to achieve operational goals. additionally, an active participation in CAPA facilitation is required</span><br/><br/><b>Your role:</b></p><ul><li>Supervises day-to-day operations of the QMS team, ensuring all quality processes are executed efficiently and in compliance with company policies and other necessary requirements.</li><li>Manages the deployment and maintenance of QMS processes in the assigned area/ areas such as document control, training, and internal audits, ensuring they are effective, compliant, and aligned with both regulatory requirements and business needs.</li><li>Monitors and reports on the effectiveness of QMS processes by analyzing performance metrics, identifying trends, and developing action plans to address gaps, enhance compliance, and improve overall quality.</li><li>Prepares for and supports external audits and inspections by ensuring all necessary documentation is available and providing detailed responses to audit findings.</li><li>Facilitates cross-functional collaboration to resolve quality-related issues, working closely with other departments to ensure alignment and effective problem-solving.</li><li>Manages the documentation and resolution of non-conformance reports (NCRs), ensuring systematic tracking, effective resolution, and implementation of preventive measures to avoid recurrence.</li><li>Conducts risk assessments and manages risk mitigation activities, identifying potential risks to product quality and QMS integrity, and developing strategies to minimize their impact.</li><li>Drives continuous improvement initiatives within the QMS, proposing and implementing enhancements to processes, tools, and systems to improve overall quality performance and operational efficiency.</li><li>Addresses difficult to moderately complex issues or problems, requiring the evaluation of identifiable factors, following established processes and operational policies in selecting methods and techniques for obtaining solutions.</li><li>Guides and mentors the QMS team, actively contributing to employee selection, performance management, compensation management, career development, and overseeing operational processes.</li><li>Participates in training sessions to stay updated on quality standards and QMS procedures, actively engaging in learning opportunities to enhance understanding of industry regulations and best practices.</li><li>Manages CAPAs as CAPA engineer</li></ul><p><br/><b>You're the right fit if:</b> (4 x bullets max)<br/><b>1. Experience- </b>10+yrs of experience in Medtech industry.<br/><b>2. Skills-</b></p><p><b>* German writing/speaking - preferred</b></p><p><b>* English writing/speaking skills - must</b><br/>• Regulatory Requirements<br/>• Quality Management Systems (QMS)<br/>• Project Management<br/>• Data Analysis &amp; Interpretation<br/>• Process Improvements<br/>• Technical Writing<br/>• Training Content Development</p><p><b>3. Education</b>- <span>Bachelor's / master’s degree, in engineering/science field or equivalent.</span><br/><b>4. Anything else-</b> <span>Master's in areas such as Quality Management Systems, Quality Audits or equivalent in highly regulated <span>environments/industries</span> such as MD, Pharma, Automotive.</span><br/><br/><b>How we work together</b><br/>We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week.<br/>Onsite roles require full-time presence in the company’s facilities.<br/>Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.<br/>Indicate if this role is an office/field/onsite role.<br/><b>About Philips</b><br/>We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.<br/>• Learn more about <a href="https://www.philips.com/a-w/about.html" rel="noopener noreferrer" target="_blank">our business</a>.<br/>• Discover <a href="https://www.philips.com/a-w/about/our-history.html" rel="noopener noreferrer" target="_blank">our rich and exciting history</a>.<br/>• Learn more about <a href="https://www.philips.com/a-w/about/environmental-social-governance/our-purpose" rel="noopener noreferrer" target="_blank">our purpose</a>.<br/>If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care <a href="https://www.careers.philips.com/global/en/our-culture" rel="noopener noreferrer" target="_blank">here</a>.</p><p><span>#LI-PHILIN</span></p>

Philips

Quality Control Engineer

<p>Lead Associate - Transactional Quality (PTP/Accounts Payable/AP) - Pune - REF82876F_2025192999</p><h4>Company Description</h4><p>WNS (Holdings) Limited (NYSE: WNS), is a leading Business Process Management (BPM) company. We combine our deep industry knowledge with technology and analytics expertise to co-create innovative, digital-led transformational solutions with clients across 10 industries. We enable businesses in Travel, Insurance, Banking and Financial Services, Manufacturing, Retail and Consumer Packaged Goods, Shipping and Logistics, Healthcare, and Utilities to re-imagine their digital future and transform their outcomes with operational excellence.We deliver an entire spectrum of BPM services in finance and accounting, procurement, customer interaction services and human resources leveraging collaborative models that are tailored to address the unique business challenges of each client. We co-create and execute the future vision of 400+ clients with the help of our 44,000+ employees.</p><h4>Job Description</h4><p>1 to 3 years of experience in call auditing, quality assurance Special Skills Good Understanding of Quality Management System and Good Communication, analytical &amp; listening skills, Should be able to do Client and Stakeholder Management , Excellent People Management Skills along with Feedback giving Skills and Ability to drive Quality Initiatives, Projects and Improvements Job Description '• Call monitoring and Evaluation (Live or recorded calls)• Agent Feedback and Coaching Support• Conduct process documentation as per ISO standards• Conduct &amp; review sampling strategy in the team• Conduct root cause analysis for process improvements• Conduct MSA as per schedule.• Drive &amp; conduct process compliance• Drive &amp; conduct audits (pre-post duties)• Conduct base lining &amp; analyze CTQs• Conduct measurement system analysis.• Drive brainwave initiative in the team• Conduct quality related trainings• Team-up with BBs / QAM’s to be a co-facilitator of projects/initiatives• Drive open forums/best practice sharing sessions• YB six sigma improvement project to be certified• Successfully complete ISO training. Working on the product &amp; helping the team to achieve deadlines. Provide timely reports, updates and system entries as required by the internal and external management. Understand and abide by the importance of discipline, punctuality &amp; protocol '</p><h4>Qualifications</h4><p>Commerce Graduate and above</p><h4>Experience Level</h4>Entry Level

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