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Executive, Quality Assurance
About Apotex Inc.Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.For more information visit: <a href="http://www.apotex.com/">www.apotex.com</a>. <h4>Job Summary</h4><ul><li>IPQA activities.</li><li>Warehouse QA activities</li><li>MMaR’ S / MPaR’s Review.</li></ul><h4>Job Responsibilities</h4><ul><li>Line clearance of Various in process stage such as Dispensing, Granulation, Compression, Coating, Packaging and Sampling.</li><li>Routine monitoring of all functional area to ensure adherence to the SOPs.</li><li>Co-ordination &amp; Ensuring timely execution of Sampling activity of Raw and Packing materials.</li><li>Co-ordination of daily activities in Manufacturing and packaging areas.</li><li>Create signature and methods for raw materials by using Truscan RM analyzer.</li><li>Approved / Rejected labels affixing for API, Excipients, Primary packing and secondary packing materials finished goods and operation supplies.</li><li>Verification of Temperature and Relative Humidity reports generated from TESTO software.</li><li>Co-ordination &amp; ensuring timely execution of in-process activities for manufacturing and Packaging.</li><li>Coordination for implementation of CAPA.</li><li>In-process checks during manufacturing &amp; packaging stage, Performance of AQL, collection of samples as applicable and trending of AQL.</li><li>Sampling of validation &amp; commercial batch, Shelf life expiration date (SLED), Bulk completion date (BCD), sampling, Hold time study sample, In-process samples/Finished product samples, Collection, storage, and disposal of Reserve Sample.</li><li>Preparation, Review and updating of standard operating procedure.</li><li>Planning, co-ordination, and sampling of Raw and Packaging materials.</li><li>Co-ordination for Process validation &amp; cleaning validation execution.</li><li>Approved/ Rejected labels affixing for API, Excipients, Primary and Secondary packaging materials.</li><li>Swab/Rinse sampling for the cleaning verification &amp; validation programme, cleaning &amp; verification of sampling thief’s &amp; accessories.</li><li>Co-ordination for in-house and external calibration.</li><li>Review of Master Manufacturing Records &amp; Master Packing records &amp; logbooks.</li><li>Works as a member of a team to achieve all outcomes.</li><li>Performs all work in accordance with all established regulatory and compliance and safety requirements.</li><li>Preparation for regulatory audits and making the compliance for the same.</li><li>To ensure that the impact of any risk reduction measures is not detrimental to the systems, facilities, utilities, equipment, or processes.</li><li>Create a culture which values trust and provides the opportunity for Employee development and growth in pursuit of our purpose and demonstrating our core Values – Collaboration, Courage, Perseverance and Passion.</li><li>Utilize your networks to attract and hire talent in a comprehensive, differentiated, and consistent manner essential to our continued growth; then, onboard new employees by providing a consistent experience that reflects the values and commitments made to candidates during the hiring process.</li><li>Ensure adherence of team members (direct reports) with all compliance programs and company policies and procedures.</li><li>All other duties as assigned.</li></ul><h4>Job Requirements</h4><ul><li>Education<ul><li>Bachelor of Pharmacy/ Science or any equivalent degree.</li></ul></li><li>Knowledge, Skills and Abilities:<ul><li>Should possess good communication and interpersonal skills along with Computer efficacy in MS-Office and Internet</li></ul></li><li>Experience:<ul><li>Minimum 02 Years of experience in GMP Regulated Pharmaceutical industry.</li></ul></li></ul> At Apotex, we are committed to fostering a welcoming and accessible work environment, where all everyone feels valued, respected, and supported to succeed. We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation. <h4>Experience Level</h4>Executive Level

Apotex Pharmachem India Pvt Ltd

Quality Assurance Executive

Manager- Quality Management1.    Quality Assurance Planning: Developing and implementing quality assurance plans and procedures to ensure that electric motors meet specified quality standards and requirements.2.    Quality Control Processes: Quality control processes throughout the manufacturing or assembly process of electric motors, including incoming materials inspection, in-process inspections, and final product testing.3.    Supplier Quality Management: Collaborating with suppliers to establish quality requirements for raw materials, components, and parts used in electric motors. Conducting audits and assessments to ensure supplier compliance with quality standards.4.    Product Testing and Validation: Establishing testing protocols and procedures to validate the performance, durability, and safety of electric motors. Analyzing test data and identifying areas for improvement.5.    Root Cause Analysis: Investigating quality issues or defects in electric motors to identify root causes and implement corrective and preventive actions to prevent recurrence.6.    Documentation and Reporting: Maintaining accurate records of quality control activities, test results, and compliance documentation. Generating reports and communicating quality performance metrics to management and relevant stakeholders.7.    Continuous Improvement: Leading continuous improvement initiatives to enhance the quality, efficiency, and reliability of electric motors. Implementing best practices and adopting new technologies or methodologies to drive quality excellence.8.    Conducting type testing on electric motors according to relevant industry standards (e.g., IEC 60034 series) and customer specifications.9.    Performing electrical, mechanical, and environmental tests to verify the design characteristics and capabilities of the motor.10.  Developing and implementing routine testing procedures for electric motors to ensure ongoing performance and reliability11.  Conducting routine tests on motor samples or production batches to monitor key parameters such as insulation resistance, winding resistance, insulation quality, vibration levels, and temperature rise.12.  Maintaining test equipment and instrumentation to ensure accuracy and reliability of test results.13.  Collaborating with production, quality assurance, and engineering teams to address any quality issues or non-conformities identified during Motor Inspection &amp;  testing14. Interpretation and evaluation of PT, MT, RT, LT, VT and UT test results.Requirement profile :à    Formal education                      :   BE (Mechanical)                                                               à    Professional experience        -      in years                            :  12 Yearsà    Special skills                           :  Sound knowledge of Routine and Type testing of Electric Motor.Defined Competencies :<ul><li>Familiar to International Electrotechnical Commission (IEC) IEC 60034 series aspects related to rotating electrical machines, including induction motors.</li><li>NDE Level II qualification in VT, PT, MT, UT, RT</li><li>Familiar to ASME Section IIA, III, V, VIII, IX standards.</li><li>Knowledge of Electric Motor Mechanical and Electrical Inspections &amp; processes.</li><li>Planning and coordination.</li><li>Problem solving and decision making</li><li>Effective communication [ verbal &amp; written]</li></ul><h4>Experience Level</h4>Mid Level

KSB Company

Quality Manager

Sr. Associate, Quality Compliance<h4>Career Category</h4>Quality<h4>Job Description</h4>ABOUT AMGENAmgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today.ABOUT THE ROLERole Description:The senior associate will work within R&amp;D Quality’s Business Intelligence and Data Analytics (BIDA) team to help deliver actionable information and recommendations to key leaders and stakeholders by maintaining and expanding our data pipelines, tools, and reporting. This role contributes to ensuring Amgen’s pursuit of life-saving medication is done with the highest regard for quality and compliance to regulations. Roles &amp; Responsibilities:As an integral team member working globally with BIDA, other R&amp;D Quality team members, and R&amp;D Quality stakeholders to ensure quality across our trials and compliance with GxP regulations and other requirements:<ul><li>Extract and clean data from internal systems for regular and ad hoc reporting, including data pipeline creation and maintenance</li><li>Generate, validate, and deliver KPIs, quality metrics, and performance indicators used across the R&amp;D Quality landscape</li><li>Investigate and analyze metric trends, anomalies, and operational insights</li><li>Design, build, and maintain Tableau dashboards for operational monitoring, compliance reporting, and executive summaries</li><li>Develop and maintain Python scripts used for data processing, transformation, and report automation</li><li>Help create reusable components for common data analysis tasks and documentation.</li><li>Ensure version control and proper documentation of scripts and workflows.</li></ul>Basic Qualifications and Experience:<ul><li>Master’s degree and 7-10 years in Pharma and Biotechnology R&amp;D Quality OR</li><li>Bachelor’s degree and 10-15 years of years in Pharma and Biotechnology R&amp;D Quality.</li></ul>Functional Skills:Must-Have Skills:<ul><li>Exceptional attention to detail and accuracy in all deliverables.</li><li>Ability to work independently and proactively in a fast-paced environment.</li><li>Proficiency with Tableau or similar data visualization tools</li><li>Familiarity with Python or other object-oriented programming language</li><li>Familiarity with SQL and Databricks</li><li>Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and virtual collaboration tools (e.g., Teams)</li><li>Effective communication, critical thinking and problem-solving</li><li>Experience in conducting data analyses and translating data sets into actionable insights</li></ul>Good-to-Have Skills:<ul><li>Familiarity with project management tools and methodologies</li><li>Knowledge of GCP, GLP and/or GPvP</li><li>Familiarity with Databricks and SQL</li><li>Experience working in a multinational environment with global teams.</li><li>Experience within Biotech/pharmaceutical Research</li><li>Independent and teamwork capabilities</li></ul>Soft Skills:<ul><li>Excellent verbal and written communication skills</li><li>High degree of professionalism and interpersonal skills</li><li>Strong problem-solving abilities and adaptability to changing priorities</li><li>Collaborative mindset and ability to build positive relationships across diverse teams</li><li>Resilience, discretion, and the ability to thrive under pressure</li></ul>.<h4>Experience Level</h4>Senior Level

Amgen Technology Private Limited

Quality Assurance Officer

Manager, Process Excellence & ChangeJob Description :Job Title: Knowledge Management Center of Excellence (CoE) LeadAbout the Function: Our Global Business Operations (GBO) team are facilitators, providing strategic, financial, and business services that are essential to the day-to-day performance of our business. With a team of over 2,000 dedicated and passionate people supporting 21 markets across the world, we have offices in Bangalore, Budapest, Bogota, and Manila.Our global remit offers huge learning opportunities. We encourage learning and development in skills needed now and in the future across digital, industry, professional, and domain. Wherever you start, you’ll be rewarded with a world view and the recognition you deserve in our inclusive and supportive culture.Job Title: Knowledge Management Center of Excellence (CoE) LeadLevel: Diageo L5ALocation: Bangalore, IndiaReports To: Senior Manager- Quality (L4B)Role Purpose:We are seeking a seasoned Knowledge Management Leader with 10–15 years of experience in the CPG/Process industry, who can drive the strategic development and execution of a global Knowledge Management CoE. The leader will partner with Global Process and Capability Owners, business units, operating/functional leaders, subject matter authorities (SMEs), L&amp;D, HR and other partners to build, deploy and drive knowledge management processes and practices. This role is pivotal in enabling, developing and implementingknowledge management strategies to enhance the organization's operational efficiency and innovation.Strategic Leadership·       Develop and implement an extensive knowledge management strategy aligned with Diageo's business objectives.·       Handle and maintain the enterprise-wide process taxonomy and documentation standards using technology applications and platforms.·       Champion the adoption and integration of knowledge management tools and platforms to enhance knowledge accessibility, process visibility, and decision-making.·       Oversee the collection, curation, organization, and maintenance of a centralized, accessible, and accurate knowledge repository.·       Collaborate with cross-functional teams including Digital &amp; Technology, Global Process Owners (GPOs), and Business Excellence to embed knowledge management practices.·       Develop a knowledge-sharing culture by facilitating collaboration, leading communities of practice, and promoting continuous learning.·       Strategic partner and organisational change at multiple levels of organizational hierarchy to drive partnership with business units, subject matter authorities), and partners to identify knowledge gaps and ensure content aligns with user needProcess &amp; Technology Integration·       Oversee the deployment, integration, maintenance of process/knowledge management tools to streamline operations/knowledge management.·       Ensure standard methodologies in process documentation, standardization, and optimization.·       Design and deliver training programs to build documentation and knowledge management capabilities across global teams.Governance &amp; Compliance·       Establish governance frameworks to ensure compliance with global standards in knowledge management.·       Establish governance frameworks to ensure consistency, accuracy, and compliance in knowledge assets across markets.·       Supervise adherence to policies related to data integrity and security.·       Supervise knowledge management effectiveness through important metrics and analytics, driving continuous improvement and innovation in knowledge practices.Collaboration &amp; Customer Engagement·       Collaborate with cross-functional teams to identify knowledge gaps and opportunities for improvement.·       Engage partners at all levels to promote the value of effective knowledge management practices.Team Development &amp; Leadership·       Lead a team of knowledge management professionals, providing mentorship and development opportunities.·       Drive performance through clear objectives, feedback, and recognition.Qualifications &amp; Experience:·       Bachelor’s or master’s degree in business administration, Information Systems, or related field.·       10-15 years of experience in process/knowledge management domains.·       Experience in knowledge management processes using tools like ARIS/SAP Signavio/Celonis etc.·       Strong leadership skills with experience leading cross-functional teams.·       Excellent communication skills with the ability to influence at all organizational levels.·       Strong understanding of process principles, documentation standards, and taxonomy frameworks.·       Experience in leading global KM initiatives and handling knowledge repositories.·       Analytical attitude with the ability to interpret data and drive insights.·       Fluent in English; additional languages (e.g., Spanish, Hungarian) are a plus.Skills &amp; Competencies:·       Expertise in process modelling standards such as BPMN.·       Strong analytical skills with an ability to translate complex data into actionable insights.·       Proficiency/certifications in project management methodologies (e.g. PMP/Prince II).·       Certifications in Lean Six Sigma &amp; Business Process Quality Management·       Ability to motivate change within large organizations and PROSCI Change Management certification can be an advantage.Success Factors:·       Strategic problem solver with a hands-on approach to execution.·       Passionate about process management, knowledge sharing, and digital enablement.·       Collaborative leader who thrives in a matrixed, global environment.·       Detail-oriented with a commitment to quality and continuous improvement.Barriers to Success:·       Lack of attention to detail and process rigor·       Poor communication and partner engagement·       Inability to adapt to digital platforms and tools·       Weak time management and prioritization skillsFlexible Working Statement: Flexibility is key to our success. From part-time and compressed hours to different locations, our people work flexibly in ways to suit them. Talk to us about what flexibility means to you so that you’re supported from day one.Diversity statement: Our purpose is to celebrate life, every day, everywhere. And creating an inclusive culture, where everyone feels valued and that they can belong, is a crucial part of this.We embrace diversity in the broadest possible sense. This means that you’ll be welcomed and celebrated for who you are just by being you. You’ll be part of and help build and champion an inclusive culture that celebrates people of different gender, ethnicity, ability, age, sexual orientation, social class, educational backgrounds, experiences, mindsets, and more.Our ambition is to create the best performing, most trusted and respected consumer products companies in the world. Join us and help transform our business as we take our brands to the next level and build new ones as part of shaping the next generation of celebrations for consumers around the world.Feel inspired? Then this may be the opportunity for you. If you require a reasonable adjustment, please ensure that you capture this information when you submit your application.Worker Type :RegularPrimary Location:Bangalore Karle Town SEZAdditional Locations :Job Posting Start Date : 2025-10-08<h4>Experience Level</h4>Senior Level

Diageo India Pvt Ltd

Sales Operations / Enablement Executive

Quality Analyst E&M ProfeeJob Family:Coding Quality OP (India) Travel Required:None Clearance Required:NoneJob Posting What We Offer:Guidehouse offers a comprehensive, total rewards package that includes competitive compensation and a flexible benefits package that reflects our commitment to creating a diverse and supportive workplace.About GuidehouseGuidehouse is an Equal Opportunity Employer–Protected Veterans, Individuals with Disabilities or any other basis protected by law, ordinance, or regulation.Guidehouse will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of applicable law or ordinance including the Fair Chance Ordinance of Los Angeles and San Francisco.If you have visited our website for information about employment opportunities, or to apply for a position, and you require an accommodation, please contact Guidehouse Recruiting at 1-571-633-1711 or via email at <a href="mailto:RecruitingAccommodation@guidehouse.com" rel="noopener noreferrer" target="_blank">RecruitingAccommodation@guidehouse.com</a>. All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodation.All communication regarding recruitment for a Guidehouse position will be sent from Guidehouse email domains including @guidehouse.com or <a href="mailto:guidehouse@myworkday.com" rel="noopener noreferrer" target="_blank">guidehouse@myworkday.com</a>.  Correspondence received by an applicant from any other domain should be considered unauthorized and will not be honored by Guidehouse.  Note that Guidehouse will never charge a fee or require a money transfer at any stage of the recruitment process and does not collect fees from educational institutions for participation in a recruitment event. Never provide your banking information to a third party purporting to need that information to proceed in the hiring process.If any person or organization demands money related to a job opportunity with Guidehouse, please report the matter to Guidehouse’s Ethics Hotline. If you want to check the validity of correspondence you have received, please contact <a href="mailto:recruiting@guidehouse.com" rel="noopener noreferrer" target="_blank">recruiting@guidehouse.com</a>. Guidehouse is not responsible for losses incurred (monetary or otherwise) from an applicant’s dealings with unauthorized third parties.Guidehouse does not accept unsolicited resumes through or from search firms or staffing agencies. All unsolicited resumes will be considered the property of Guidehouse and Guidehouse will not be obligated to pay a placement fee.

Guidehouse

Quality Analyst

GCP Quality Compliance Manager<h4>Career Category</h4>Quality<h4>Job Description</h4>Join Amgen’s Mission of Serving PatientsAt Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.GCP Quality Compliance ManagerWhat you will doLet’s do this! Let’s change the world! In this vital role you will provide critical support to the Process Quality function by assisting in the implementation, monitoring, and continuous improvement of Amgen’s R&amp;D Quality Management System (QMS).Accountabilities: <ul><li>Assist in maintaining and improving the QMS by helping to track, document, and implement quality initiatives, ensuring that procedures and processes meet regulatory requirements.</li><li>Contribute to the collection, analysis, and reporting of quality metrics (KPIs, KQIs), helping to identify trends, risks, and areas for continuous improvement.</li><li>Provide hands-on support to the Senior Manager in ensuring procedural compliance with GCP standards and other regulatory requirements across R&amp;D.</li><li>Act as a liaison between the Process Quality function and Global Networks supporting smooth collaboration and exchange of information.</li><li>Provide support for Serious Breach Process</li><li>Perform risk assessments of process, vendors and functions</li><li>Identify data quality indicators/trends, identify areas of weakness/gaps, recommend and implement corrective actions</li><li>Coordinate activities related to site/sponsor inspections and audits - preparation, conduct and close out and response generation</li></ul>Key Capabilities:<ul><li>Understanding of SOP/Standards management and methods/technology used to drive knowledge management across a diverse R&amp;D environment</li><li>Communicate effectively</li><li>Develops innovative and creative output based on interpretation and analysis</li><li>In-depth disciplinary knowledge; uses business insight and subject matter expertise</li><li>Employs project management techniques</li><li>Thorough understanding of business priorities, strategy and direction</li><li>Integrates trends, data and information into plans, deliverables and recommendations</li><li>Manages root cause analysis and corrective/prevent action completion follow-up</li><li>Acts as a technical expert in GCP</li><li>Employs critical thinking skills</li><li>Able to separate critical from non-critical issues</li><li>Strong attention to detail and proficiency in managing data and reports.</li><li>Actively seek and implement innovative and proactive quality oversight methodologies (e.g., risk-methods leveraging AI and Natural Language Processing, and other advanced data analytics methods).  </li></ul>What we expect of youWe are all different, yet we all use our unique contributions to serve patients. The individual we seek has technological literacy and leadership skills and has these qualifications.Basic Qualifications:<ul><li>Doctorate degree OR</li><li>Master’s degree and 2 years of Quality/Compliance/Process Management experience OR</li><li>Bachelor’s degree and 4 years of Quality/Compliance/Process Management experience OR</li><li>Associate’s degree and 8 years of Quality/Compliance/Process Management experience Or</li><li>High school diploma / GED and 10 years of Quality/Compliance/Process Management experience</li></ul>Preferred Qualifications:<ul><li>2 years or more experience in Quality Management, Quality Assurance, or other relevant areas of the pharmaceutical/biotech industry where risk-based quality management and quality by design are a core responsibility.</li><li>Solid understanding of SOP/Standards management and methods/ technology used to drive knowledge management across a diverse R&amp;D environment.</li><li>Thorough understanding of Clinical R&amp;D activities and Global Regulations.</li><li>Strong analytical, critical thinking, and decision-making abilities.</li><li>Strong Process Mind and analytically oriented - experience with process monitoring, including applying analytical methods and modern technology to enable signal detection and quality improvement.</li><li>Proven team player – takes direction and can rapidly learn and support a hard-working team, making rapid decisions and communicating them promptly.</li><li>Excellent verbal and written communication skills - demonstrates strong business writing abilities and active listening.</li><li>Capability to understand and articulate technical concepts and literature in spoken and written English.</li></ul>What you can expect from usAs we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:<ul><li>A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts</li><li>A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan</li><li>Stock-based long-term incentives</li><li>Award-winning time-off plans</li><li>Flexible work models, including remote and hybrid work arrangements, where possible</li></ul>Apply now and make a lasting impact with the Amgen team.careers.amgen.comIn any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.Application deadlineAmgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status..<h4>Experience Level</h4>Mid Level

Quality Control Manager

Quality Management System & Infrastructure ManagerQuality Management System &amp; Infrastructure ManagerCompany:Boeing India Private LimitedOverviewAs a leading global aerospace company, Boeing develops, manufactures and services commercial airplanes, defense products and space systems for customers in more than 150 countries. As a top U.S. exporter, the company leverages the talents of a global supplier base to advance economic opportunity, sustainability and community impact. Boeing’s team is committed to innovating for the future, leading with sustainability, and cultivating a culture based on the company’s core values of safety, quality and integrity.Technology for today and tomorrowThe Boeing India Engineering &amp; Technology Center (BIETC) is a 5500+ engineering workforce that contributes to global aerospace growth. Our engineers deliver cutting-edge R&amp;D, innovation, and high-quality engineering work in global markets, and leverage new-age technologies such as AI/ML, IIoT, Cloud, Model-Based Engineering, and Additive Manufacturing, shaping the future of aerospace.People-driven cultureAt Boeing, we believe creativity and innovation thrives when every employee is trusted, empowered, and has the flexibility to choose, grow, learn, and explore. We offer variable arrangements depending upon business and customer needs, and professional pursuits that offer greater flexibility in the way our people work.We also believe that collaboration, frequent team engagements, and face-to-face meetings bring together different  perspectives and thoughts – enabling every voice to be heard and every perspective to be respected.  No matter where or how our teammates work, we are committed to positively shaping people’s careers and being thoughtful about employee wellbeing.With us, you can create and contribute to what matters most in your career, community, country, and world. Join us in powering the progress of global aerospace.Boeing India has an exciting opportunity for a Quality Management System &amp; Infrastructure Manager to join our team located in Bengaluru or Chennai, India.We are looking for a First Line Quality Manager to support our QMS. This is a fast-paced position supporting Boeing India and encompasses work across multiple Business Units. The candidate will be coordinating with all levels and functions of and  will be managing our Quality Management Systems (QMS) compliance.Position Responsibilities:<ul><li>Manages employees who evaluate and ensure that products, services and processes comply with customer contract requirements, engineering requirements, company procedures and government regulations.</li><li>Develops and executes business plans, policies and procedures and develops organizational and technical strategies to improve performance.</li><li>Provides education and coaching on the Quality System.</li><li>Acquires and manages resources and leads process improvements.</li><li>Develops and maintains relationships and partnerships with customers, stakeholders, peers, partners, suppliers and direct reports.</li><li>Manages, develops and motivates employees.</li><li>Lead risk management, quality control/assurance efforts, nonconformance management and root cause analysis</li><li>Ensure adherence to the documented processes and procedures</li></ul>Basic Qualifications (Required Skills/Experience):<ul><li>Bachelor’s degree or higher is required</li><li>5+ years of experience in quality</li><li>Demonstrated knowledge of Quality Management Systems (QMS) and experience executing compliance audits, corrective action systems, and KPI-based risk monitoring</li><li>Experience with root-cause problem solving, corrective/preventive action processes, and tools for tracking closure (e.g., audit systems, PASA or equivalent)</li><li>Strong leadership, cross-functional collaboration, and communication skills with proven ability to develop talent, drive accountability, and report status to stakeholders and executives</li></ul>Preferred Qualifications:<ul><li>AS9100 experience</li><li>Skilled at interpreting and deriving insights from data</li><li>Experience in aerospace/regulated environments (FAA/airworthiness processes) or prior authorization to make airworthiness determinations</li><li>Formal training and practical experience with continuous improvement methods (Lean, Six Sigma) and deploying quality systems for new product / MBU introduction</li></ul>Typical Education &amp; Experience:Bachelor’s degree or higher with 13+ years of related work experience OR Masters of Engineering and 12+ years of related experience.Relocation:This position offers relocation based on candidate eligibility.Visa Sponsorship:Employer will not sponsor applicants for employment visa status.Language Requirements:Not ApplicableEducation:Bachelor's Degree or EquivalentRelocation:This position offers relocation based on candidate eligibility.Security Clearance:This position does not require a Security Clearance.Visa Sponsorship:Employer will not sponsor applicants for employment visa status.Contingent Upon Award ProgramThis position is not contingent upon program awardShift:Not a Shift Worker (India)<h4>Experience Level</h4>Mid Level

Boeing India Pvt Ltd

Team Lead, Quality AssuranceWe are looking for a Team Lead Quality Assurance Engineer to join our team in India. This is an amazing opportunity to work on different projects with our QA team, which has various competencies to compete and learn together. We have a great skill set in the team related to Manual Testing, Test Automation, Performance Testing, DevOps, Accessibility Testing, and Security Testing. We need someone experienced in both Automation and Manual testing, covering Application UI, Services, and Data. Ideally, you should have a strong background in writing Automation tests using Java and TypeScript.About You – experience, education, skills, and accomplishments:<ul><li>Bachelor’s degree in engineering or master’s degree (BE, ME, B Tech, MTech, MCA, MS)</li><li>At least 8 years of demonstrable experience in Test Automation, UI, API automation, Performance Engineering, and Accessibility Testing</li><li>At least 5 years for experience in Test Automation: Strong coding &amp; debugging skills in tools and technologies like Java, Selenium, Cucumber, TestNG, JUnit, Rest Assured, Robot Framework, etc. Preferable experience in JavaScript-based tools, Playwright</li><li>At least 5 years for experience in Performance Engineering: Strong experience in performance engineering, including hands-on with at least one tool (Netload, JMeter, or LoadRunner) along with a very good understanding of browser-side performance testing tools and analyzing skills</li><li>Accessibility Testing: Good to have skills for accessibility engineering of enterprise products, including WCAG and 508 guidelines. Have worked on any one of the tools like WAVE, AXE, SiteImprove, AChecker, etc., and can automate other open-source tools for accessibility</li><li>Clear understanding of the testing pyramid, understanding of functional and non-functional aspects of testing</li><li>Designing the architecture of test automation frameworks and implementing the framework in new projects after analyzing the best test automation tool and technology</li><li>Have worked and significantly contributed to automation using CI/CD pipeline using Jenkins</li><li>Demonstrable work done in product development &amp; dev in test with teams spread across different locations worldwide</li><li>Good working experience with GIT, Jenkins, Bitbucket, JIRA, etc.</li><li>Working familiarity with cloud platforms like AWS</li><li>Should be able to mentor and assist junior team members &amp; ramp-up new joiners</li><li>Clear understanding of Agile &amp; Kanban development approaches</li><li>Familiarity with working with test and defect management tools like Zephyr, Testrail</li><li>Demonstrable work done in product development &amp; quality with teams spread across different locations worldwide</li></ul>It would be great if you also had:<ul><li>Experience in an Agile environment</li><li>A proactive approach to learning new skills</li><li>Experience with Browser Developer tools</li><li>Familiarity with Elasticsearch/MongoDB/NoSQL querying</li></ul>What will you be doing in this role?<ul><li>This is an 80% coding and 20% people management role</li><li>Design, implement, and execute automated tests</li><li>Debug, fix, and optimize existing automated tests</li><li>Maintain manual test scripts as needed using the Zephyr tool in JIRA</li><li>Utilize bug tracking and report generating tools</li><li>Communicate test progress, results, and other relevant information to leadership and stakeholders</li><li>Configure regression frameworks to run against different instances</li><li>Collaborate closely with Software Engineers, Product, and Project Management</li></ul>Hours of Work<ul><li>Regular working hours in India</li></ul>At 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 Associate

Senior Quality Engineer - IntermediateEquifax is where you can power your possible. If you want to achieve your true potential, chart new paths, develop new skills, collaborate with bright minds,  and make a meaningful impact, we want to hear from you.You are passionate about quality and how customers experience the products you test. You have the ability to create, maintain and execute test plans in order to verify requirements. As a Quality Engineer at Equifax, you will be a catalyst in both the development and the testing of high priority initiatives. You will develop and test new products to support technology operations while maintaining exemplary standards. As a collaborative member of the team, you will deliver QA services (code quality, testing services, performance engineering, development collaboration and continuous integration). You will conduct quality control tests in order to ensure full compliance with specified standards and end user requirements. You will execute tests using established plans and scripts; documents problems in an issues log and retest to ensure problems are resolved. You will create test files to thoroughly test program logic and verify system flow. You will identify, recommend and implement changes to enhance effectiveness of QA strategies. What you will do<ul><li>With limited oversight, use your experience and knowledge of testing and testability to influence better software design, promote proper engineering practice, bug prevention strategies, testability, accessibility, privacy, and other advanced quality concepts across solutions. </li><li>Develop test strategies, automate tests using test frameworks and write moderately complex code/scripts to test solutions, products and systems. </li><li>Monitor product development and usage at all levels with an eye for product quality. </li><li>Create test harnesses and infrastructure as necessary.</li><li>Demonstrate an understanding of test methodologies, writing test plans, creating test cases and debugging.</li></ul> What experience you need<ul><li>Bachelor's degree in a STEM major </li><li>Webservices testing, UI application testing, and automation.</li><li>2-5 years of software testing experience</li><li>Able to create automated test based on functional and non-functional requirements</li><li>Self-starter that identifies/responds to priority shifts with minimal supervision.</li><li>Experience in Webservices testing and Web application Testing</li><li>Good to have experience working with Salesforce applications.</li><li>Software testing tools like Cucumber, Selenium, Java, Python</li><li>Software testing, performance, and quality engineering techniques and strategies</li><li>Testing technologies: JIRA, Confluence</li><li>Cloud technology: Any cloud exposure (GCP Preferred)</li></ul> What could set you apartYou should also have the ability to demonstrate performance of our Success Profile skills, including: <ul><li>Attention to Detail - Create thorough and accurate documentation of all work including status updates to summarize project highlights; validating that processes operate properly and conform to standards; Organizes own work, following established standards and processes.</li><li>Automation - Automate defined test cases and test suites per project and plan; Develop test automation using automation frameworks</li><li>Collaboration - Collaborate with peers, Product Owners and Test Lead to understand product functionality and specifications to create effective test cases and test automation</li><li>Execution - Define methods of bug prevention, testability strategies and other advanced testing concepts; Define test cases and create scripts based on assessment and understanding of product specifications and test plan; Create automation test plans; Execute test cases that validate product functionality per the test plan; Record testing results and defects with details to reproduce the issue in JIRA and Zephyr</li><li>Quality Control - Create defects as a result of test execution with correct severity and priority; Analyzes discrete sets of information from functional and non-functional test execution; Assist in integrating test automation in the CI environment; Performance / Resilience: Understanding application and network architecture as inputs to create performance and resilience test strategies and plans for each product and platform. Conducting the performance and resilience testing to ensure the products meet SLAs / SLOs</li><li>Quality Focus - Ensure communications are thorough and accurate for all work documentation including status updates; Peer review created test automation with other SDETs; Monitor product development by using JIRA stats to measure product quality; Review all requirements/acceptance criteria to assure completeness and coverage</li><li>Risk Mitigation - Work with team leads to track and determine prioritization of defects fixes</li></ul>We offer a hybrid work setting, comprehensive compensation and healthcare packages, attractive paid time off, and organizational growth potential through our online learning platform with guided career tracks.Are you ready to power your possible?  Apply today, and get started on a path toward an exciting new career at Equifax, where you can make a difference!Primary Location: IND-Trivandrum-Equifax Analytics-PECIND-Pune-Equifax Analytics-PECFunction: Function - Tech Dev and Client ServicesSchedule: Full time<h4>Experience Level</h4>Mid Level

Equifax Credit Information Services Pvt Ltd

Quality Engineer

Senior Engineer - Testing<h4>About SLK</h4>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. 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.<h4>BASIC INFORMATION ON THE POSITION</h4> Position Name: Senior Engineer - Testing <h4>Mandatory/Required Skills &amp; Location</h4>Location:Mandatory/Required Skills : <h4>PURPOSE OF THE ROLE</h4> This role is responsible for reviewing Software Requirements, identify test scenarios, design &amp; execute Test cases, create automated test scripts, Defect Management &amp; ensure high quality test deliverables to customer as per project timelines. Assist Test Engineers &amp; Trainees on test scenario, test design &amp; provide inputs to Test Leads on Test estimations, Strategy &amp; planning. <h4>KEY RESPONSIBILITIES AND ACCOUNTABILITIES</h4> <ul><li>Analyse the project test requirements &amp; document test scenarios. Raise clarifications &amp; get it clarified from BAs/Customers</li><li>Derieve Test Scenarios, Develop Test cases, Execute Test cases, review test cases prepared by junior and peers, report Testing status and also create &amp; execute automated scripts.</li><li>Assist Test Leads on Test Estimates, Strategy &amp; Planning, monitoring progress and timely delivery</li><li>Participate in DRB meetings, team meetings and  customer calls to provide clarifications or issue resolutions</li><li>Ideas for automation, process improvement (Project/Unit/Org), productivity improvement or develop accelerator/tools/macros</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 initiatives of 6 days training minimum per year.</li><li>Mentor &amp; Coach Test Engineer &amp; Juniors in the team.</li><li>Ensure cost savings for the firm by ensuring high utilisation of one's own time and implementation of newer ideas</li></ul><h4>EDUCATION QUALIFICATION</h4> <ol><li>BE/B.Tech/ME/M.Tech/MCA/MSc</li><li>Certification: ISTQB</li></ol><h4>MINIMUM EXPERIENCE REQUIRED</h4> <ol><li>4+ years of testing experience</li></ol><h4>DOMAIN/ FUNCTIONAL SKILLS</h4> <ul><li>Testing Concepts/Principles, Test Design, Test Execution techniques, Tools - HPQC or any equivalent Test Management tools, Peer Reviews, Understanding of test planning and automation</li><li>BFSI/M&amp;SC domain experience</li><li>Analytical skills, Logical Reasoning</li></ul><h4>Experience Level</h4>Senior Level

SLK Software Private Limited

Junior Test Engineer

Associate Quality Compliance<h4>Career Category</h4>Quality<h4>Job Description</h4>Role Name: Associate Quality ComplianceDepartment Name: R&amp;D QualityRole GCF: 3ABOUT AMGENAmgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. ABOUT THE ROLERole Description:The Controlled Documentation Associate plays a critical role in supporting Amgen’s R&amp;D Quality Management System through the execution and maintenance of controlled document workflows. This role ensures that R&amp;D controlled documents, such as SOPs and work instructions, are developed, maintained, and retired in compliance with global standards and GCP regulations. The associate will collaborate across functions to facilitate document approval processes, conduct quality checks, and support inspection readiness activities.Roles &amp; Responsibilities:<ul><li>Execute and track workflows for creation, revision, and obsoletion of documents with the controlled document management system (CDOCS).</li><li>Perform controlled document impact analysis in support of business requests and initiatives.</li><li>Maintain document metadata in CDOCS.</li><li>Conduct quality checks, editing, and proofreading of documents for consistency and compliance.</li><li>Monitor document workflows, notify stakeholders of pending tasks, and follow up to ensure timely completion.</li><li>Support inspections and audits by retrieving and compiling requested documents.</li></ul>Basic Qualifications and Experience:<ul><li>Masters Degree in Sciences or related field with 2-6 years exp in Pharmaceutical/Biotechnology/Clinical research</li></ul>Functional Skills:Must-Have Skills:<ul><li>Strong attention to detail with proven ability to perform quality reviews.</li><li>Working knowledge of document control tools and best practices.</li><li>Excellent verbal and written communication skills.</li><li>Ability to manage document workflows and prioritize tasks.</li></ul>Good-to-Have Skills:<ul><li>Experience working in a multinational environment with global teams.</li><li>Experience using CDOCS or equivalent electronic document management system.</li></ul>Soft Skills:<ul><li>Strong problem-solving abilities and adaptability to changing priorities.</li><li>Strong attention to detail and accuracy.</li><li>Excellent organization and coordination skills.</li><li>Clear and concise communication abilities.</li><li>Team-oriented and proactive approach.</li></ul>EQUAL OPPORTUNITY STATEMENTAmgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation..<h4>Experience Level</h4>Mid Level

Senior Executive, QA Validation & Engineering
About Apotex Inc.Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.For more information visit: <a href="http://www.apotex.com/">www.apotex.com</a>. <h4>Job Summary</h4>Shall involve actively in the execution and act as a reviewer of validation and qualification documents in the validation section. Be a subject matter expert in the validation section and shall ensure compliance in all the activities performed.<h4>Job Responsibilities</h4><ul><li>General </li><li>Preparation of Validation Master Plan (VMP) and SOP’s related to validations section</li><li>Co-ordination, assessment and review of change control, notification, deviation in the quality management system related to validation activities.</li><li>Coordinate and participate in the quality risk management (QRM) exercise related to facility, utility, equipment and process carried out in the facility.</li><li>Shall carryout gap assessment against global procedures/regulatory requirements and address gaps ensuring compliance.</li><li>Act as coordinator for periodic self-inspection of validation section for evaluation of the effectiveness of the quality systems.</li><li>Maitaining adherence to regulatory requirements and ensure the validation section is ready for audit anytime.</li><li>Create a culture which values trust and provides the opportunity for Employee development and growth in pursuit of our purpose and demonstrating our core Values – Collaboration, Courage, Perseverance and Passion.</li><li>All other duties as assigned. </li></ul><ul><li>Qualification</li><li>Act as Subject matter expert (SME) for qualification and validation protocols related to equipments, utilities</li><li>Review/approval of periodic requalification documents pertaining to equipment / system / utilities and instrument of various departments across ARPL.</li><li>Review/approval of annual schedules for calibration, qualification status review, qualification, AMC, cleaning &amp; sanitization, preventive maintenance and filter replacement etc.</li><li>Approval of layouts, yearly &amp; monthly schedules, to be added planners, New logbook request etc.</li><li>Cleaning Validation</li><li>Act as Subject matter expert (SME) for cleaning validation</li><li>Responsible for evaluation of products for cleaning validation, preparation of cleaning validation matrix, performing MACO calculation, preparation of Equipment Cleaning Process Design Document (ECPDD), .cleaning validation protocols and reports, Quarterly/Annual monitoring reports for cleaning validation</li><li>Responsible to carryout cleaning validation activities in eResidue Pro software application</li><li>Process Validation</li><li>Act as Subject matter expert (SME) for process validation</li><li>Responsible for review/approval of documents related to process validation for demonstration batch, Optimization batch, Technical Risk Assessment, Process Performance Qualification, packaging validation protocols and reports, Continuous process verification and hold time study protocols and reports.</li></ul> <h4>Job Requirements</h4><ul><li>Education :
<ul><li>Master degree in Pharmacy/ Science or any equivalent degree.</li></ul></li><li>Knowledge, Skills and Abilities
<ul><li>Possess sound knowledge in Qualification of Equipment, facility and utilities.</li><li>Maintains good Interpersonal skills and communication skills.</li><li>Strives to drive projects related to Qualification effectively</li></ul></li><li>Experience
<ul><li>Minimum 6 years of experience in GMP Regulated pharmaceutical industry</li></ul></li></ul>At Apotex, we are committed to fostering a welcoming and accessible work environment, where all everyone feels valued, respected, and supported to succeed. We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation. <h4>Experience Level</h4>Senior Level

Senior Process and Compliance ManagerJob Description SummaryResponsible for ensuring operational excellence related to clinical trial activities within Translational Clinical Oncology (TCO). Track progress to key quality indicators (KQIs), Quality Plan and overall compliance to applicable processes and regulations. Lead and assist in the development and implementation of process improvement initiatives within the function; ensure changes are adequately communicated and managed. Work collaboratively with clinical QA (CQA) and appropriate line functions to ensure that TCO upholds high quality standards. Job Description Major accountabilities: <ul><li>Accurate and timely execution of process improvement and quality initiatives as measured by meeting key milestones effectively.</li><li>Successful implementation of process improvements as measured by sustainable changes and improved efficiency.</li><li>Increased compliance with relevant processes.</li><li>Establish business partnerships with all relevant TCO functional groups, CQA, training and other LFs as required.</li><li>Training programs implemented in a timely fashion, and tracked to ensure compliance and maintenance</li></ul><h4> Impact on the Organization: </h4><ul><li>Improved quality of outputs</li><li>Increased compliance with SOP, GCP and training</li><li>Decreased audit/inspection findings</li><li>Efficient use of resources through operational effectiveness</li></ul><h4>Additional Details</h4><ul><li>KQIs - Responsible to track, report and reinforce adherence to applicable performance measures. Support in recommending corrective actions based upon report outputs and root cause analysis; and support implementing training/communication as applicable to ensure remediation (preventative actions). Support Clinical Trial Quality Risk Management (CTQRM) review by evaluating studies to ensure adherence to CTQRM SOP and follow-up with respective study leads.</li><li>SOPs - provide input into new SOPs/WPs on behalf of TCO as applicable, may serve as subject matter expert. Contribute to identifying training opportunities and ensuring compliance with new SOPs and Working Practices. Track quality issues and ensure their documentation within the quality event management system and implementation of corrective actions. Support the implementation and tracking of compliance to the clinical trial processes.</li><li>Quality Plan - Ensure that actions required of TCO are appropriately tracked.  Support the conduct of self-assessments for TCO in conjunction with CQA. Proactively ensure procedural deficiencies within TCO are corrected and prevented. Liaise with BR TM and CS&amp;I and appropriate Development LFs to ensure quality outcomes.</li><li>Process Expertise – identify or support the identification of procedural gaps and their correction with process improvements where applicable. Represent TCO/BR in cross-functional initiatives aiming for continual process improvement and ensuring a compliance focused environment either by direct involvement or by ensuring appropriate TCO/BR representation. May serve as Managed Access Program Champion.</li><li>Training -Support training/communications to assure understanding of new processes or findings.  Assure remediation. Identify gaps and assign action where needed to promptly gain compliance. Assist with change management activities related to new processes or organizational changes. Support/organize timely Lessons Learned sessions.</li><li>Compliance – As applicable based on assignment, ensure Corrective Actions Preventative Actions (CAPA) commitments are adequate, submitted and completed in a timely manner. Initiate and document root cause investigations of critical issues. Support inspection preparation and inspection readiness.  Ensure the timely submission and completion of adequate Corrective Actions Preventative Actions (CAPA). Ensure audit and inspection outcomes requiring corrective action are managed.</li><li>Act as TCO Protocol Review Committee Manager, as assigned: run PRC Office independently (meetings and agenda planning, uploading of documents in review system), maintain the PRC SharePoint site, system owner of the TCO PRC submission tracker, providing training and access and working with IT on system updates; maintain revisions to the PRC charter.</li><li>Act as BR-DOC Manager, as assigned – manage end-to-end document QC function with BR Translational Medicine – BR Doc function. Provide vendor management, track submissions and provide guidance to TCO teams.</li><li>As assigned, participate as a reviewer on the TCO Protocol Review Committee or assist with quality checks of documents (protocols, ICFs, etc) as appropriate per TCO process.</li><li>Escalate issues to TCO management and CQA in a timely manner.</li></ul> Minimum Requirements: Work Experience: <ul><li>A minimum of 5 years of relevant pharmaceutical clinical development experience</li><li>Extensive knowledge of clinical development process, GCP and clinical quality management; including strong understanding of regulation and guidance for clinical studies</li><li>Proficiency/Fluency in English</li><li>Experience working in matrix environment and in global teams.</li><li>Excellent interpersonal, problem-solving, negotiation and conflict resolution skills</li><li>Excellent organizational skills, as well as predisposition to quality management and process improvement</li><li>Excellent communicator and presenter (oral and written).</li></ul> Education: <ul><li>Bachelor of Science (BS) or advanced degree in scientific discipline or equivalent education in life science/healthcare required</li></ul> Languages :<ul><li>English.</li></ul> Skills DesiredAnalysis, Databases, Decision Making Skills, Operations, Problem Solving Skills, Reporting, Team Management, Waterfall Model<h4>Experience Level</h4>Senior Level

Novartis India

Process Manager

Quality Manager, VPJoin us as a Quality Manager<ul><li>We’ll look to you to provide direction and leadership on all quality matters across the platform or domain including adoption and compliance with the bank's standards and policies</li><li>This is an opportunity to act as a key contributor in making sure that work packages transition seamlessly from development into live environments</li><li>Hone your knowledge of quality best practices and collaboration and stakeholder management skills</li><li>We're offering this role at vice president level</li></ul><h4>What you'll do</h4>In this key role, you’ll be making sure that only well designed and built work packages get through quality testing. You’ll aim to get it right first time for our customers through innovative service and solutions, using automation as an accelerator and working closely with stakeholders in an Agile and collaborative environment. We’ll also look to you to produce comprehensive and robust quality strategies and detailed quality test plans, enabling the continual flow of work packages across the domain, platform value stream or programme.Additionally, you’ll be:<ul><li>Taking accountability for all aspects of quality across both run and change and business as usual activity within the assigned platform or domain</li><li>Overseeing the output quality from all testing phases owned and making sure it meets the requirements of each quality test strategy</li><li>Making sure defects are detected and prioritised, based on impact, and resolved at the earliest possible moment and before the last responsible moment</li><li>Undertaking end-to-end test management including planning, risk, issue, dependency management, lessons learnt and governance</li><li>Reviewing all key collateral relating to delivery and making sure it is of sufficient quality and with no gaps or duplication</li></ul><h4>The skills you'll need</h4>We’re looking for someone with strong knowledge and understanding of quality standards, quality best practices, and our risk and controls framework. You’ll also need high levels of knowledge and demonstrable application of modern testing and quality practices and techniques used with Agile methodologies.Additionally, we’ll be looking for:<ul><li>Expertise in JIRA, Zephyr, Confluence, creating reports and dashboard</li><li>Experience in functional and non-functional testing such as system, system integration, user, load, volume, stress, security, accessibility, compatibility, penetration and back-out</li><li>The ability to relate everyday work to the strategic vision of the feature, platform, domain and enterprise teams, with a strong focus on business outcomes</li><li>The ability to communicate complex technical concepts clearly to peers and management</li><li>Good collaboration and stakeholder management skills</li></ul>Hours45Job Posting Closing Date:31/10/2025<h4>Experience Level</h4>Executive Level

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Quality Assurance Jobs In Hassan - 358 Verified Vacancies

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Quality Assurance Associate

Process Manager

Quality Manager