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Senior Executive Quality Control     <h4>JOB DESCRIPTION:</h4>Followings will be the Core Job Responsibilities of the position holder:   Primarily responsible for support in routine calibration, Scheduled Calibration, Maintenance / External Calibration of all instruments and equipment's in QC. Responsible for preparation and management of Reference Standard /Working Standard /Primary Standard. Responsible for Preparation and management of Preventive maintenance Schedule. Responsible for Qualification of all instruments in QC. Support for analysis of In process, SFG, Finished Goods, Raw material /PM &amp; stability Sample, and related documentation as per GLP and GMP in time. Co-ordinate for AMC and external tie-ups for equipment and keep record of maintenance of equipment. Preparation and management of Volumetric solution and Test Solution Ensuring compliance to the EPD Global guidelines. Breakdown management related to all instruments in QC and update related documents. Ensuring the timely update in the documents as per the Pharmacopoeia! amendments. Coordination for the timely availability of the amended documents. Facing internal audits and External audits and ensuring compliance. On job training related activities in QC. Analysis of additional samples for laboratory investigation. Preparation of SOP, Specification &amp; STP. Responsible for work which is allotted by Section Head.      The base pay for this position is N/AIn specific locations, the pay range may vary from the range posted.     <h4>JOB FAMILY:</h4>Operations Quality     <h4>DIVISION:</h4>EPD Established Pharma        <h4>LOCATION:</h4>India &gt; Village Mauza : Baddi     <h4>ADDITIONAL LOCATIONS:</h4>     <h4>WORK SHIFT:</h4>Standard     <h4>TRAVEL:</h4>Not specified     <h4>MEDICAL SURVEILLANCE:</h4>Not Applicable     <h4>SIGNIFICANT WORK ACTIVITIES:</h4>Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)               <h4>Experience Level</h4>Senior Level

Abbott India Ltd

Quality Control Manager

Specialist, Quality Assurance EngineeringCalling all innovators – find your future at Fiserv.We’re Fiserv, a global leader in Fintech and payments, and we move money and information in a way that moves the world. We connect financial institutions, corporations, merchants, and consumers to one another millions of times a day – quickly, reliably, and securely. Any time you swipe your credit card, pay through a mobile app, or withdraw money from the bank, we’re involved. If you want to make an impact on a global scale, come make a difference at Fiserv.Job TitleSpecialist, Quality Assurance EngineeringWhat does a successful Tech Lead, Quality Assurance Engineer do? A successful Tech Lead, Quality Assurance Engineer with .Net programming language at Fiserv plays a pivotal role in our mission to deliver reliable, high-quality financial services technology. They ensure that our products meet high standards of functionality, reliability, and performance, helping our clients provide dependable services to their customers. Working alongside a team of dedicated professionals, they contribute to the continuous improvement of our testing processes and drive the innovation needed to stay ahead in the fintech industry.What you will do:<ul><li>Develop and execute test plans and test cases to ensure the quality and performance of Fiserv products.</li><li>Design and implement automated testing frameworks and scripts.</li><li>Collaborate with software developers and product managers to identify test requirements, design test strategies, and troubleshoot issues.</li><li>Conduct thorough regression testing when bugs are resolved.</li><li>Monitor testing processes and ensure that software releases are timely and of high quality.</li><li>Document and report defects, and work with developers to resolve them.</li><li>Stay up-to-date with the latest industry trends and technologies to improve testing practices.</li></ul>What you will need to have:<ul><li>BE, BTech or MCA and/or equivalent military experience.</li><li>8+ years of experience in software testing and quality assurance.</li><li>6+ years of experience in automated testing tools such as Selenium, JUnit, or similar.</li><li>8+ years of experience with various testing methodologies and types of testing (functional, non-functional, regression, etc.).</li><li>6+ years of experience in .Net programming language and scripting languages like Python,or JavaScript.</li></ul>What would be great to have:<ul><li>7+ years of experience in performance and load testing using tools like Selenium.</li><li>6+ years of experience with continuous integration and continuous deployment (CI/CD) tools such as Jenkins or Travis CI.</li><li>6+ years of experience with API testing tools, e.g., Postman, SoapUI.</li><li>6+ years of experience with version control systems like Git.</li><li>ISTQB Certification in the relevant domain.</li></ul>Perks at Work:<ul><li>We’re #FiservProud of our commitment to your overall well-being with a growing offering of physical, mental, emotional, and financial benefits from day one.</li><li>Maintain a healthy work-life balance with paid holidays, generous time off policies, including Recharge &amp; Refuel time for qualifying associates, and free counseling through our EAP.</li><li>Plan for your future with competitive salaries, the Fiserv 401(k) Savings Plan, and our Employee Stock Purchase Plan.</li><li>Recognize and be recognized by colleagues with our Living Proof program where you can exchange points for a variety of rewards.</li><li>Prioritize your health with a variety of medical, dental, vision, life and disability insurance options and a range of well-being resources through our Fuel Your Life program.</li><li>Advance your career with training, development, certification, and internal mobility opportunities.</li><li>Join Employee Resource Groups that promote our diverse and inclusive culture where associates can share perspectives, exchange ideas, and elevate careers.</li></ul>Thank you for considering employment with Fiserv.  Please:<ul><li>Apply using your legal name</li><li>Complete the step-by-step profile and attach your resume (either is acceptable, both are preferable).</li></ul>Our commitment to Diversity and Inclusion:Fiserv is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, gender, gender identity, sexual orientation, age, disability, protected veteran status, or any other category protected by law. Note to agencies:Fiserv does not accept resume submissions from agencies outside of existing agreements. Please do not send resumes to Fiserv associates. Fiserv is not responsible for any fees associated with unsolicited resume submissions.Warning about fake job posts:Please be aware of fraudulent job postings that are not affiliated with Fiserv. Fraudulent job postings may be used by cyber criminals to target your personally identifiable information and/or to steal money or financial information. Any communications from a Fiserv representative will come from a legitimate Fiserv email address.<h4>Experience Level</h4>Senior Level

Fiserv India Pvt Ltd

QA Engineer

Manager, Global Quality Complaint SurveillanceWorking with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" rel="noopener noreferrer" target="_blank">careers.bms.com/working-with-us</a>.Key ResponsibilitiesResponsible for managing and reporting of accurate and on time Global Quality metrics for Product Quality Complaints (PQC) in a fast-paced environment that support Tier Councils, Product Quality Complaint compliance &amp; trending across the organization, internal &amp; regulatory audits. Expertise with data management and analysis using electronic software solutions, eg VEEVA, Tableau, SpotFire, and Microsoft Office, with focus on Excel, PowerPoint, and SharePoint.Responsible to maintain a high level of knowledge &amp; understanding of Pharmaceutical/Biologic Quality Assurance, Device Quality Assurance, cGood Manufacturing Practices as applicable in global GMP regulations (including FDA, EMA, MHRA, PMDA, ENVISA, TGA).Responsible to develop &amp; maintain tools and dashboards in support of PQC trending, data surveillance and PQC user support.Responsible to provide PQC data assessments, highlighting trends, signals and risks and business critical information related to Product Quality Complaint data to Quality leadership in a timely fashion. Data &amp; trend assessments will be communicated with stakeholders in a manner commensurate with risk, and enabling appropriate action taking to protect BMS and our patients. Responsible to complete required training and provide support for Product Complaints, Product Surety and Quality Serialization business process activities.You are accountable for other key activities that support the business such as:<ul><li>SharePoint design, data requests/analysis, and providing communication of trends, signals and risks in addition to business critical information to leadership</li><li>Maintain expertise on PQC data management at BMS, including data sources, data quality, data management, data users</li><li>Report at appropriate intervals (weekly, monthly, quarterly, year-on-year etc) metrics on key compliance indicators related to PQC performance and procedural compliance (for example on-time closure, increasing/decreasing trends by product/defect category/market etc).</li><li>Review signals and trends that may present a risk to the organization and/or to our patients. Engage with PQC management and appropriate stakeholders to identify corrective actions. Align with PQC management for escalations to Quality leadership.</li><li>Provide recommendations and communications based on output from analytical tools and visualizations.</li><li>Provide risk assessment support for PQC processes, data management and related activities</li><li>Continuously improve process for assessment and reporting PQC data to drive consistency and understanding of Quality compliance-focused metrics</li><li>Use Operational Excellence and similar approaches to support the design of metric tools that facilitate proactive discussion and provide visibility/transparency to drive continuous improvement, prioritization and product quality related decisions</li><li>Lead teams in the development of tools and reports to optimize and standardize metrics</li><li>Lead collection and review of PQC data in response to health authority requests</li><li>Lead collection and review of PQC data in support of audit requests (internal and external audits)</li><li>Lead metrics initiatives related to product quality complaint programs and processes</li><li>Facilitate and drive standards for communication, management and visibility of product quality support metrics</li><li>Implementation and timely update of information to ensure content is current and accurate</li><li>Establish appropriate procedural documents for product quality support metrics</li><li>Cross train in other areas of the Global Quality organization to assist the business in developing its employees</li><li>Develop and maintain high quality relationships with key stakeholders</li><li>Work on multiple projects at one time and manage priorities based on timelines</li><li>Work independently with a high degree of professional integrity, be highly organized, and be detail-oriented</li><li>Perform duties as aligned with PQC management</li></ul>Qualifications &amp; ExperienceDegree/Certification/LicensureBachelor of Science degree in data analytics/statistics/biostatistics, engineering, chemistry, biology, or other quantitative field.Advanced degree preferred.Required Competencies<ul><li>Fluent in English, with proven professional working proficiency in English for reading, writing and speaking</li><li>Excellent communication with management, peers, and other functional areas</li><li>Excellent ability to analyse data to extract useful information and trends, and to translate data to effective messaging to  stakeholders and leaders supporting effective decision-making</li><li>Ability to work well cross-functionally with stakeholders</li><li>Ability to influence positively in a matrix environment</li><li>Proven ability to understand complex processes/problems and propose alternate solutions</li><li>Customer and partner focus, including the ability to listen to and incorporate feedback from key stakeholders</li><li>Demonstrated Enterprise mindset to be able to think and act across functions and divisions</li><li>Demonstrated ability to work in a matrixed organization with a range of technically, culturally, and geographically diverse teams and to influence areas not under direct control to achieve objectives and effectively communicate challenging goals and objectives</li><li>Excellent teamwork, interpersonal, and communication skills, with the ability to communicate and collaborate with employees and management at all levels and through various formats</li><li>Demonstrated strategic thinking capability and ability to balance conflicting priorities</li><li>Ability to provide innovative ideas or alternatives that create value including seeking new information and external insights without compromising compliance</li><li>Ability to clearly articulate analytical needs to functional partners</li></ul>Experience – Responsibility and minimum number of years<ul><li>A minimum of 5 years of experience in a data analytical role, or in a Quality role where data analytics was a key component in the pharmaceutical/ biotech/ device industry</li><li>Strong working knowledge/experience with systems such as QMS, SAP/ERP, Veeva</li><li>Experience with understanding how to respond to trend signals within the context of quality surveillance</li><li>Strong problem solving skills are required</li><li>Strong program and project management</li><li>Ability to manage multiple, simultaneous projects</li><li>Thorough understanding of Quality Risk Management</li><li>Mastery of relevant Quality compliance processes and regulations</li><li>Understanding of technical areas related to pharmaceutical and/or biological manufacturing, chemical and/or biochemical analyses, microbiological</li></ul>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" rel="noopener noreferrer" target="_blank">adastaffingsupport@bms.com</a>. Visit <a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">careers.bms.com/</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">eeo</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">-accessibility</a> to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: <a href="https://careers.bms.com/california-residents/" rel="noopener noreferrer" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.<h4>Experience Level</h4>Mid Level

Bristol-Myers Squibb India Pvt Ltd

Quality Specialist

Manager - Quality
In a world where customers consistently interact with your brand across multiple channels-including digital and social-we at Startek value our ability to effectively garner those interactions and CX insights, analysing, unlocking, and providing intelligence that drives digital transformation and further revenues for you, our client.Put simply: we break down the complexity of your customer lifecycle and help your customers build and sustain emotional connections with your brand.Our tech-enabled and Human assisted digital solutions build both on your CX requirements and our business transformation expertise and willingness to consistently pivot, innovate, and take advantage of new digital technologies.It’s a robust approach. We’ve partnered with global brands for over 3 decades now -working with them across their consumer value chain and providing new age customer experience solutions and insights that are helping them define and reach their target audiences with greater efficiency and better value for every dollar spent.Our partnerships have always been about more than building emotional connections with customers; they are about using artificial intelligence, omnichannel orchestration and providing CX insights &amp; technologies, that has the power for digital transformation We do this across 46 locations in 13 countries, with over 40,000 employees managing almost half a billion customer interactions every year for over 150 clients in different industries.*** DISCLAIMER***With the increase of remote positions since COVID, many companies have seen an increase in false representation recruiters and offering fraudulent positions/pay rates that do not exist.These messages are from anonymous sources and crafted to appear as they are being sent from Startek recruiters.  All communication from Startek will have an email address from  “startek.com”.  Additionally, a scam message can request funds or other personal information prior to the offer letter being released.  This is not a standard operating procedure for Startek to be employed with the organization.Startek is not responsible for any fraudulent representing the company.  <h4>Experience Level</h4>Mid Level

Startek

Quality Manager

QUALITY CONTROL ANALYST IAt TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. <h4>Job Overview</h4>"Coordinates with the suppliers and the internal stakeholders to qualify products and the process and ensure compliance with the organization's requirements.<h4>Job Requirements</h4><ul><li>Compiling and documenting statistical data from the testing processes to confirm compliance with the organization's established standards and identify improvements.</li><li>Assisting with the evaluation of the quality of raw materials and finished goods and supporting with various quality control assays.</li><li>Working with various teams to facilitate internal and external quality issue resolution.</li><li>Collaborating with multiple stakeholders to understand inspection techniques, support internal and external audits, and attend training sessions on quality concepts and tools.</li></ul><h4>What your background should look like</h4>Generally requires Bachelors degree in appropriate field or local equivalent.<h4>Competencies</h4>
Values: Integrity, Accountability, Inclusion, Innovation, Teamwork<h4>Experience Level</h4>Entry Level

TE Connectivity India Pvt Ltd

Quality Control Assistant

Assistant Manager - Quality
In a world where customers consistently interact with your brand across multiple channels-including digital and social-we at Startek value our ability to effectively garner those interactions and CX insights, analysing, unlocking, and providing intelligence that drives digital transformation and further revenues for you, our client.Put simply: we break down the complexity of your customer lifecycle and help your customers build and sustain emotional connections with your brand.Our tech-enabled and Human assisted digital solutions build both on your CX requirements and our business transformation expertise and willingness to consistently pivot, innovate, and take advantage of new digital technologies.It’s a robust approach. We’ve partnered with global brands for over 3 decades now -working with them across their consumer value chain and providing new age customer experience solutions and insights that are helping them define and reach their target audiences with greater efficiency and better value for every dollar spent.Our partnerships have always been about more than building emotional connections with customers; they are about using artificial intelligence, omnichannel orchestration and providing CX insights &amp; technologies, that has the power for digital transformation We do this across 46 locations in 13 countries, with over 40,000 employees managing almost half a billion customer interactions every year for over 150 clients in different industries.*** DISCLAIMER***With the increase of remote positions since COVID, many companies have seen an increase in false representation recruiters and offering fraudulent positions/pay rates that do not exist.These messages are from anonymous sources and crafted to appear as they are being sent from Startek recruiters.  All communication from Startek will have an email address from  “startek.com”.  Additionally, a scam message can request funds or other personal information prior to the offer letter being released.  This is not a standard operating procedure for Startek to be employed with the organization.Startek is not responsible for any fraudulent representing the company.  <h4>Experience Level</h4>Mid Level

Quality Engineer (Tester)Project Role : Quality Engineer (Tester) Project Role Description : 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. Must have skills : TOSCA Testsuite Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education 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 engaging with various teams to ensure that testing processes are efficient and effective, while also focusing on continuous improvement and automation strategies. You will be responsible for creating automated scripts and supporting data and environment configuration, ensuring that the quality of the applications meets the highest standards. Additionally, you will participate in code reviews and monitor defects, contributing to a culture of excellence and collaboration within the team.
 
Roles &amp; Responsibilities: 
- Expected to be an SME.
- Collaborate and manage the team to perform.
- Responsible for team decisions.
- Engage with multiple teams and contribute on key decisions.
- Provide solutions to problems for their immediate team and across multiple teams.
- Facilitate knowledge sharing sessions to enhance team capabilities.
- Develop and implement best practices for testing and automation.
 
Professional &amp; Technical Skills: 
- Must To Have Skills: Proficiency in TOSCA Testsuite.
- Strong understanding of test automation frameworks and methodologies.
- Experience with continuous integration and continuous deployment practices.
- Familiarity with API testing tools and techniques.
- Ability to analyze and interpret complex data sets to inform testing strategies.
 
Additional Information: 
- The candidate should have minimum 5 years of experience in TOSCA Testsuite.
- This position is based at our Bengaluru office.
- A 15 years full time education is required.

Accenture India Private Limited

QA Test Engineer

Quality Engineer<h4>Position:</h4>Quality Engineer<h4>Job Description:</h4>* Detailed Description of the Job Profile (Role and Responsibility)<ul><li>Performing quality audits as per CMMI / ISO 13485 / ISO 62304 / IEC 14971</li><li>Understanding of software lifecycle</li><li>Medical QMS with regulatory requirements knowledge</li><li>Guiding and facilitating projects for effective process &amp; metrics implementation</li><li>Work product reviews for quality and process</li><li>Writing, updating and implementation of quality management system</li><li>Conducting trainings</li><li>Prepare &amp; Present Management Reviews</li><li>Defining processes and conduct Quality Management System related activities</li><li>Review documents (such as proposals / SoWs /</li></ul>Project plans) to ensure the quality<ul><li>Take other global initiatives such as external audits, Customer surveys, knowledge management, training</li></ul>* Technical Skill [Required]<ul><li>CMMI</li><li>ISO 13485 / ISO 62304 / IEC 14971</li><li>AS 9100</li><li>ISO 9001</li><li>Experience in Process Definition/ Improvement/ Implementation</li><li>Software Quality Assurance</li><li>Proficiency in Project Management</li><li>Sound knowledge of Product Lifecycle Management</li><li>Understanding of audit cycles and processes</li><li>Good in MS Excel, Project, Word and Presentation</li><li>Six Sigma</li><li>VBA Programming</li></ul>* Soft Skills [Required]<ul><li>Positive attitude &amp; Good team player</li><li>Excellent communication (written and oral), presentation &amp; interpersonal skill</li></ul><ul><li>Ability to work independently and collaboratively</li></ul><ul><li>Ability to prioritize and manage work to critical project timelines in a fast-paced environment</li></ul><h4>Location:</h4>IN-GJ-Ahmedabad, India-Ognaj (eInfochips)<h4>Time Type:</h4>Full time<h4>Job Category:</h4>Supply Chain Services<h4>Experience Level</h4>Senior Level

Arrow Electronics India Pvt Ltd

Quality Engineer

Operational Excellence & Continuous Improvement Analyst - CCCLocation:Bengaluru, Karnataka, IndiaJob ID: R0098601Date Posted:2025-09-22Company Name:HITACHI ENERGY TECHNOLOGY SERVICES PRIVATE LIMITEDProfession (Job Category):Quality ManagementJob Schedule: Full timeRemote:NoJob Description:Mission Statement: This role will focus driving Lean &amp; Six Sigma practices, improve &amp; implement the communication strategy across all three Hubs &amp; Front offices. Main Accountabilities:<ul><li>Working on the identification and execution of Continuous Improvement plans and oversees tactical projects completion.</li><li>Assisting with CI program administration and coordination, including the development and execution of CI deployment plans.  </li><li>Accurately forecasting projects value targets and costs in alignment with business strategy. </li><li>Using advanced knowledge to develop and manage CI project plans for projects with moderate cost, risk and assures project goals and objectives are attained and sustained. </li><li>Identifying and documenting variances from project goals and objectives, as well as communicates status reports, issue logs and risk areas to necessary stakeholders promptly.</li><li>Ensuring the stated values from projects are delivered to bottom line.  </li><li>Tracking and reporting the value creation and develops sustainment plans to ensure sustainable results. </li><li>Using experience to drive process improvement initiatives throughout CP&amp;O. </li><li>Independently managing the daily execution of value stream processes, sub processes, and work streams to ensure completion of milestones on time and within scope of projects. </li></ul><ul><li>Setting and continually managing project goals and objectives with team members and other stakeholders. </li></ul><ul><li>Driving collaboration and team-based problem solving. Identifies, monitors, and implements CI best </li></ul>practices.  <ul><li>Working with cross-functional teams to select and implement tools and methodologies that will enable capturing best practices. </li><li>Driving CI capability and culture change for CP&amp;O through best practice sharing, vocal advocacy, and visible leadership, which includes identification and implementation of opportunities. </li><li>Driving best in the class performance management framework for all business lines. </li><li>Prepares presentations, communications, and training materials to enable change management and success of CI project initiatives. </li><li>Conducting Training, workshops and driving a Lean six Sigma Culture.</li><li>Work closely with stakeholders to understand communication needs and improve internal messaging.</li><li>Develop and implement communication strategies that align with organizational goals.</li><li>Create presentations, invitations, and communication packs for project stakeholders.</li><li>Draft and distribute global communications, ensuring consistency in messaging.</li><li>Support teams in crafting clear, engaging, and effective communication materials.</li><li>Coordinate with various departments to ensure seamless information flow.</li><li>Assist in organizing internal events, meetings, and stakeholder engagements.</li><li>Monitor and evaluate communication effectiveness, providing recommendations for improvement.</li></ul>Knowledge, Skills and Experience:<ul><li>Bachelor’s / master’s degree from a reputed university. </li><li>5+ years of overall experience with 2+ years in a CI role.</li><li>Strong inter-personnel, analytical, and presentation skills.</li><li>Lean Six Sigma Green Belt certification (Must).</li><li>Substantial progress toward Lean Six Sigma projects</li><li>Knowledge in Continuous Improvement methodologies, tools, trends and best practices </li><li>Technical competency in Lean Six Sigma skills, such as DMAIC, Lean, Kaizen, Root Cause Analysis (RCA) etc. </li><li>Analytical Problem-Solving skills: able to identify problems, apply structured and disciplined methodology to identify root cause, and cause- effect relationships using data </li><li>Experience with operations management, project management, or process engineering.</li><li>Strong proficiency in Microsoft Office Suite (PowerPoint, Word, Outlook).</li><li>Excellent written and verbal communication skills.</li><li>Ability to manage multiple projects and meet deadlines.</li><li>Strong interpersonal skills and the ability to collaborate effectively with diverse teams.</li><li>Experience in creating communication materials, newsletters, and reports.</li></ul><h4>Qualified individuals with a disability may request a reasonable accommodation if you are unable or limited in your ability to use or access the Hitachi Energy career site as a result of your disability. You may request reasonable accommodations by completing a <a href="https://www.hitachienergy.com/contact-us/general-inquiry?type=I+have+a+General+question" rel="noopener noreferrer" target="_blank">general inquiry form</a> on our website. Please include your contact information and specific details about your required accommodation to support you during the job application process.</h4><h4>This is solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes will not receive a response. </h4><h4>Experience Level</h4>Senior Level

Hitachi India Pvt Ltd

Senior Quality Analyst

Associate Manager Quality AssuranceROLE SUMMARY<ul><li>Responsible for reviewing documents related to product development, analytical data (including electronic data, chromatographic data, and audit trails), as well as instrument and equipment qualification</li><li>Accountable for ensuring data integrity compliance and adherence to SOPs during the review of both hard copy and electronic records</li><li>Conduct periodic system audit trail reviews and ensure compliance with 21 CFR Part 11 requirements</li><li>Liaise effectively with global BL and OQ colleagues to achieve organizational objectives</li><li>Maintain a thorough understanding of ICH quality guidelines and relevant regulatory guidance on microbiology method development pertaining to sterility, BET, CCIT, and associated development requirements</li><li>Possess in-depth knowledge regarding sterility requirements and filter validation activities in accordance with PDA technical reports</li><li>Demonstrate familiarity with requirements for sterile ANDA product development and combination products</li><li>Exhibit strong proficiency in MS Office applications, including Excel, Word, and PowerPoint presentation preparation</li></ul>ROLE RESPONSIBILITIES &amp; SKILL SETS<ul><li>Awareness of DI and ALOCA principles</li><li>Basic understanding of cGMP requirements, including 21 CFR part 210 and 211, ICH guidelines, and sterile product requirements</li><li>Maintain compliance in laboratories and during document review</li><li>Ability to perform statistical evaluation and analysis of analytical data during method development and validation review</li><li>Effective communication skills.</li><li>Adherence to discipline and self-motivation.</li><li>Participate in the implementation of new initiatives and goals within the QA function and with business line partners to support consistency, efficiency, and compliance.</li><li>Manage time to meet agreed targets and plan work activities for projects within assigned teams.</li><li>Suggest improvements and participate in continuous improvement activities.</li><li>Contribute to the development and compliance of quality and business line partner procedures</li><li>Provide support for inspection readiness efforts, internal audits, and regulatory inspections as required</li></ul>QUALIFICATIONS Education:<ul><li>Master of science in chemistry</li><li>Master of pharmacy</li></ul>Relevant experience:<ul><li> Relevant work experience in an analytical data review and Technology transfer and cGMP pharmaceutical   sterile manufacturing area</li></ul>Location: On premise   Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.Quality Assurance and Control<h4>Experience Level</h4>Mid Level

Pfizer Ltd

Quality Assurance Associate

Social AuditorJob Responsibility &amp; Accountability (Key Roles, functions &amp; accountability): <ul><li>Perform Audits as and when assigned in accordance to Client and Bureau Veritas guidelines.</li><li>Manage the operations of the station office (if assigned)</li><li>Effective communication with office staff and Audit Representative </li><li><ul><li> </li><li>•Conducting on-site audits as a leader or a member of the audit team – Performing all audit procedures,</li><li>•Fully understand and follow the client’s requirements and company SOP, WI etc.</li><li>•Guide and monitor onsite performance of Associate Auditor during audit process</li><li>•Give feedback to Trainer/N+1/Back office about performance of associate auditor</li><li>•Effective communication with office staff and factory representative</li><li>•Ensure to collect all required Images/hard copy of documents from the facility ha</li><li>•Prepare assigned audit report which are complete, comprehensive and presented</li><li>•Ensure that submit report package along with employee interview sheet/filled lis</li><li>•Ensure to respond reviewer’s query at earliest to meet report TAT to client. In any case response should not be delayed fo<ul><li>Ensure to respond client’s query at earliest. In any case response should not be delayed for more than 24 hours. In any cir</li><li>If report is assigned to you, then ensure to collect all documents/images/audit folder from co-auditors on the day of audit</li><li>Ensure to submit Alert Notification, JCS, 2 minutes safety documents, etc. within stipulated time.</li><li>Ensure to E-file all images/documents in readable condition on office server as per BV guideline and procedure within 2 w</li><li>Ensure to submit hard copy of audit folder to concern responsible person in back</li><li>Coordinate with back office staff/agents for timely arrangements for out station travelling</li><li>Ensure to submit travelling bills in timely manner (within 2 weeks of the audit).</li><li>Ensure to complete all assigned trainings in stipulated time</li><li>Ensure to reach facility within 30 minutes of office hours starts and audit is completed in stipulated working hours. Delay</li><li>Ensure confidentiality of information obtained during the course of employment in BV</li></ul></li></ul></li></ul><ul><li>Ensure to perform any job related assignment as required by N+1 or above </li></ul>Sk8      Skill:             APSCA Certified /CSCAA university degree and above or diploma in Textile/ APSCA Certification • Good command of English and local language, both oral and written. • Good knowledge of computers. • Good interpersonal communication skills. • Attention to detail and process improvement skills. • Must be confident, highly efficient and self-motivated. • Must be able to work independently as well as in a team environment. • Willingness to travel extensively.         AP <h4>Experience Level</h4>Entry Level

Bureau Veritas India Pvt Ltd

Auditor

Senior Quality Assurance EngineerWe are looking for a Senior Quality Assurance Engineer, testing to join our Quality Engineering team. This is an amazing opportunity to work on various Clarivate products and services which could include automation, manual and security aspects of testing. We have a great skill set in Test Automation using Selenium with Java, API Testing, Security Testing, Browser Stack, Performance Engineering using JMeter and many other latest technologies. We would love to speak with you if you have skills in Selenium, Java, Java Script, or Python.About You<ul><li>Bachelor’s degree in Engineering or master’s degree (BE, ME, B Tech, MTech, MCA, MS) </li><li>4+ years of experience in software automation, BDD framework, API automation and test frameworks</li><li>Good programming skills in language like Java. Strong coding &amp; debugging skills in Selenium binding with Java</li><li>Experience in version control system Git or bitbucket.</li><li>Understanding of test automation frameworks &amp; assisting/reviewing script creation </li><li>Familiarity of testing pyramid, understanding of functional and non-functional aspects of testing</li><li>Familiarity and clear understanding of Agile &amp; Kanban development approaches</li><li>Familiarity of working with test and defect management tools like JIRA and confluence.</li></ul>It would be great if you also have…<ul><li>Working familiarity with cloud tools like AWS</li></ul>What will you be doing in this role?<ul><li>This is hands on role with skill sets in automation engineering</li><li>The person will not have a dedicated team under him</li><li>Be prepared to evaluate, learn and use new tools</li><li>Work with team members in a supportive way which encourages team building and confidence with individual members </li><li>Work accurately sometimes even under pressure &amp; delivering as per the expectations </li><li>Prioritizing individual &amp; team’s workload </li></ul>Product you will be developing This intellectual property–focused product enables comprehensive IP searches, taxonomy management, and AI-driven search capabilities, supporting clients in research, innovation, and patent filing through advanced analytical data. About the TeamThe existing team is spread across India and includes Testers with strong technical and analytical skills. We have a great skill set in Java, Selenium, Python, C#, HTML5, Web API, SQL and JavaScript, to name a few of the Tools and technologies. You would be part of large QA Group responsible for delivering world class products and innovative solutions in the field of IP.Hours of WorkThis is permanent position with Clarivate. You will be working in IST time zone. 9 hours of work per day including 1-hour lunch break. We have WFO work model, flexible and employee friendly work environmentAt Clarivate, we are committed to providing equal employment opportunities for all  qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.<h4>Experience Level</h4>Senior Level

Clarivate

Quality Assurance Engineer

Supervisor, Quality Assurance - Valve Industry<h4>Job Summary:</h4><ul><li><h4>Establishing and Ensuring the System procedures are meeting the requirements of ISO 9001; ISO 14001: ISO 45001: API Q1; API Monogram, CE-PED, UKCA -PESR and other applicable Products / Certification / Marking requirements.</h4></li><li><h4>Liaison with Certifying bodies/ agency and ensure timely Certification renewal process , through expediting audits and obtain/retain the certification.</h4></li><li><h4>Coordinating with certifying bodies for new certification for product and systems.</h4></li><li><h4>Responsible for preparing, maintaining and amendment of quality management systems manual, and supporting for other manuals related to Integrated management system (ISO 14000 &amp; ISO 45001).</h4></li><li><h4>Ensure processes are in place, Train the workforce (team) and monitor for adherence of System / Customer / Product requirements, thereby ensure audits are completed without any major issues.</h4></li><li><h4>Responsible for organizing management review meetings as per plan.</h4></li><li><h4>Review and provide resources, support, and make decisions appropriately based on risk assessment / contingency plans, thereby ensure that the team is working towards the Department / Organization KPI objectives</h4></li></ul><h4>Job Responsibility:</h4><ul><li><h4>Safety and environmental requirements of the team.</h4></li><li><h4>Provide Disposition of components based on its Conformance to Purchase order requirements</h4></li><li><h4>Quality Documentation</h4></li><li><h4>Ontime clearance of GRN &amp; provide disposition – Accept, Hold, Rework, Reject</h4></li><li><h4>Conformance of Identification and traceability during receipt</h4></li><li><h4>Availability of check list, ITP, Customer specifications, work Instructions and procedures, where the activities is performed.</h4></li><li><h4>Providing Qualitative &amp; Quantitative data for analysis to Head QA.</h4></li></ul><ul><li><h4>Co-ordination with third-party inspection agencies for Inspection and scheduling activities</h4></li><li><h4>Support Quality Supervisor for his day-to-day Quality assurance/control activities.</h4></li><li><h4>Preparation of QA procedures / Project specific  technical procedure / work instructions/ documents and records and maintain as per the retention period.</h4></li><li><h4>Performing Internal Quality Audit / product and process audits, Supplier Evaluation and Re-evaluation audits as per the schedule.</h4></li><li><h4>Preparation &amp; Control of Quality Dossier, Verification of Documents</h4></li><li><h4>Ensure product readiness prior to inspection and solve quality issues, if any</h4></li><li><h4>Attend Inspections, Record observations and ensure compliance with specifications.</h4></li><li><h4>Expertise in ITP/QAP against QMS, Product standards and Customer requirements</h4></li><li><h4>Monitor route card / Traveler – Stage inspections</h4></li><li><h4>Handle customer complaints and monitor non-conformance</h4></li><li><h4>To achieve KPI metrics and data analysis for identified Gaps. Prepare / Collection of Data and communicate MR on Quality objectives, KPI metrics, MOC, Risk and Opportunity identification, Assessment and contingency plan.</h4></li><li><h4>Follow-up with departments for timely closure of Customer complaints.</h4></li><li><h4>Support NCR/CAPA process for issues arising out of inspection</h4></li><li><h4>Provide Training and awareness.</h4></li><li><h4>Adhering to safety rules &amp; regulations</h4></li></ul><h4>Job Requirement:</h4><ul><li><h4>B.E or Diploma in Mechanical / Production Engineering with 10-15 years’ experience in Quality Assurance / Control activities.</h4></li><li><h4>Lead auditor in QMS, EMS and OHSAS</h4></li><li><h4>Good work experience in Manufacturing process requirements, Customer requirements and Codes &amp; Standards.</h4></li><li><h4>Certified in NDE Level II – PT, MT, UT &amp; RT</h4></li><li><h4>Should have team management experience. (8-10 FTE's)</h4></li><li><h4>Worked in Product and Material standards ASME, ISO, ASTM, EN etc, Quality Management System, Product standards &amp; approvals.</h4></li><li><h4>Awareness of the latest applicable codes and standards.</h4></li><li><h4>Handling and implementing quality management system across the company complying to the international standards and product applicable standard.</h4></li><li><h4>Internal Auditor qualification</h4></li><li><h4>Coordinating external agencies and certifying bodies for certification renewal and new certification process.</h4></li><li><h4>Customer complaint handling , analysis, reporting and implementing the corrective actions.</h4></li><li><h4>NDE Evaluation</h4></li><li><h4>Welding Inspection -As applicable</h4></li></ul><ul><li><h4>Knowledge on requirements of ISO 9001, ISO 14001, OHSAS 18001, API SPEC Q1 &amp; API Monogram (6A, 6D and 609), PED/CE marking, and ATEX requirements.</h4></li><li><h4>Customer interaction for product approvals and Interaction with notified bodies for Certification.</h4></li><li><h4>Knowledge on Selection and Usage of appropriate Tools, Gauges &amp; Instrument.</h4></li><li><h4>Knowledge on various Problem solving techniques, Analyze problems, detect root causes and resolve issues.</h4></li><li><h4>Knowledge on SAP, MS office, Omnidocs.</h4></li></ul><h4>Experience Level</h4>Mid Level

Flowserve India Controls Pvt Ltd

Quality Assurance Officer

QA Automation Engineer•	Primary skills:Technology-&gt;Automated Testing-&gt;Test automation framework design •	Knowledge of more than one technology
•	Basics of Architecture and Design fundamentals
•	Knowledge of Testing tools
•	Knowledge of agile methodologies 
•	Understanding of Project life cycle activities on development and maintenance projects
•	Understanding of one or more Estimation methodologies, Knowledge of Quality processes
•	Basics of business domain to understand the business requirements
•	Analytical abilities, Strong Technical Skills, Good communication skills
•	Good understanding of the technology and domain 
•	Ability to demonstrate a sound understanding of software quality assurance principles, SOLID design principles and modelling methods
•	Awareness of latest technologies and trends
•	Excellent problem solving, analytical and debugging skills A day in the life of an Infoscion
•	As part of the Infosys delivery team, your primary role would be to interface with the client for quality assurance, issue resolution and ensuring high customer satisfaction. 
•	You will understand requirements, create and review designs, validate the architecture and ensure high levels of service offerings to clients in the technology domain.
•	You will participate in project estimation, provide inputs for solution delivery, conduct technical risk planning, perform code reviews and unit test plan reviews.
•	You will lead and guide your teams towards developing optimized high quality code deliverables, continual knowledge management and adherence to the organizational guidelines and processes.
•	You would be a key contributor to building efficient programs/ systems and if you think you fit right in to help our clients navigate their next in their digital transformation journey, this is the place for you!
If you think you fit right in to help our clients navigate their next in their digital transformation journey, this is the place for you!

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