14,173 Associate Qa jobs in India

Gurgaon
- 3
- 2 to 5 years
- Full Time

**Job Description**:
**Responsibilities**:

- Review and analyze system specifications to understand requirements and design comprehensive test plans.
- Identify, document, and track software defects and inconsistencies, providing detailed reports to the development team.
- Collaborate closely with developers and other stakeholders to understand software functionalities and ensure comprehensive test coverage.
- Conduct regression testing to verify that existing functionalities work as intended after code changes.
- Participate in requirement reviews, design reviews, and other quality assurance activities to provide input from a testing perspective.
- Ensure that deliverables meet quality standards and project timelines.
- Assist in the preparation of test reports and documentation for stakeholders.
- Stay updated with the latest industry trends and best practices in software testing.

**Requirements**:

- Bachelor’s degree in Computer Science, Information Technology, or a related field.
- 2-5 years of experience in manual software testing.
- Proficiency in test management software and tools.
- Strong understanding of software development life cycle (SDLC) and software testing life cycle (STLC).
- Familiarity with Agile frameworks and regression testing.
- Excellent analytical and problem-solving skills.
- Strong attention to detail and ability to work in a fast-paced environment.
- Effective communication skills, both written and verbal.
- Ability to work collaboratively in a team setting.

**Job Description Summary**
We are seeking a meticulous and detail-oriented Documentation cum Analytical Specialist . This role involves managing documentation processes and performing analytical tasks to ensure compliance with industry regulations and maintain high-quality standards.
**Job Description**
+ QMS handling like change control, deviation, OOS, Investigation, CAPA, etc.,
+ QMS trending.
+ Handling site QA documentation
+ Issuance, distribution and archival of documents.
+ Document storage management.
+ Handling compliance wire, document management system software, track wise, SAP etc.
+ Collaboration with cross functional team.
+ Providing training
+ Preparation of SOP, protocol, reports etc.
+ Knowledge in overall API QA function.
+ Internal audit experience will be added advantage.
+ Participated in USFDA regulatory inspection and arrange necessary documents as needed on timely manner.
+ Experience with electronic documentation management systems (EDMS).
+ Familiarity with quality management systems (QMS).
Soft skill:
+ Good oral and written communication.
+ Should be active and take own responsibilities.
+ Collaboration with CFT.
+ Meeting committed timeline.
+ Good knowledge in computer operation and typewriting.
Others:
+ 8 Years experience which should include min 5 years in QA
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

**Join Amgen's Mission of Serving Patients**
**At 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.**
**Position Summary:**
The AIN Sr Associate QA plays a critical role in supporting disposition related tasks across the Amgen Quality Operations Network. The Senior Associate QA will leverage industry, technical, and quality systems knowledge to provide support of business performance and GMP disposition supporting processes across the network. The position will be responsible for tasks including the key responsibilities documented below and other disposition related job functions.
This candidate will primarily work during regular working hours (9 am - 6 PM local time) to enable the business in delivering Amgen's mission to serve patients and may lead a shift-based team that provides coverage in support of the Amgen network across multiple time zones. The candidate may need to work outside of his/her routine workday to support business needs and will be responsible for determining the same for their staff. The individual will be required to work from our office located in Hyderabad India (Amgen India-AIN). The candidate will also lead the remote support from AIN to Amgen sites across multiple time zones which will include the following locations: US - California, Puerto Rico, North Carolina, Ohio, Rhode Island, Ireland - Dun Laoghaire, and Singapore.
**Key Responsibilities**
**Business Performance**
- Facilitation of Amgen disposition network meeting including meeting planning, preparation, communication of meeting notes, and action item tracking.
- Create, maintain, and report monthly disposition metrics in support of all Amgen sites.
- Create and sustain a visualization tool that displays the progress of each disposition element required for the disposition of a material and product batch.
- Monitoring of material and product batches to confirm readiness for disposition. Communicate to plants/sites when there is a material or product batch priority.
**Technical Writing and Document Management**
- Maintenance, periodic review, and revision of GMP procedures supporting global and site level disposition processes.
- Generate Production and Disposition summary to support the Annual Product Review (APR). Perform data verification, review/approval.
**Quality Systems and Clinical Disposition Process Support**
- Management and periodic review of badge access to controlled GMP areas.
- Periodic SAP security audits and access review for Amgen sites.
-Execution of GMP process for adding countries, branches, or studies to a clinical drug Product (FDP) batch in the ERP system as regulatory approvals are received.
**Inspection Request Form (IRF) pre-request support**
- Support readiness for internal and external audits and inspections including the provision of pre-inspection request documents such as disposition document lists and disposition lot lists.
-Support of information requests and response preparation during audits and inspections execution through the provision of disposition related information and data.
**Preferred Qualifications**
- Experience in project management and related systems
- Proficiency in technical writing and data visualization tools; experience with Smartsheet, Tableau, or equivalent platforms preferred.
- Strong analytical skills with the ability to interpret data and draw conclusions
- Excellent verbal and written communication skills
- Proven ability to lead and collaborate within cross-functional teams in a dynamic, fast-paced setting.
**Core Competencies**
- Organizational Agility
- Business Operations and Project Support
- Experience working in a regulated environment with knowledge of Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) requirements.
- Experience working with Quality Systems that may include enterprise resource planning (ERP/SAP), regulatory information management (RIM), controlled document management (CDOCs), change control (CCMS), deviation, and/or quality control laboratory information management systems (LIMS).
- Technical Document Drafting and Workflow Ownership
- Data Visualization, Interpretation and Analytics
**Basic Qualifications and Experience:**
- Master's degree with 5-8 years of Pharma and Biotech commercial or clinical manufacturing Quality experience.

Description

QMS handling like change control, deviation, OOS, Investigation, CAPA, etc.,

QMS trending.

Handling site QA documentation

Issuance, distribution and archival of documents.

Document storage management.

Handling compliance wire, document management system software, track wise, SAP etc.

Collaboration with cross functional team.

Providing training

Preparation of SOP, protocol, reports etc.

Knowledge in overall API QA function.

Internal audit experience will be added advantage.

Participated in USFDA regulatory inspection and arrange necessary documents as needed on timely manner.

Experience with electronic documentation management systems (EDMS).

Familiarity with quality management systems (QMS).

Soft skill:

Good oral and written communication.

Should be active and take own responsibilities.

Collaboration with CFT.

Meeting committed timeline.

Good knowledge in computer operation and typewriting.

Others:

8 Years experience which should include min 5 years in QA

Job Description

THE XACTLY STORY:

Xactly is a leading provider of enterprise-class, cloud-based, incentive compensation solutions for employee and sales performance management. We address a critical business need: to incentivize employees and align their behaviors with company goals. Our solutions allow organizations to make better strategic decisions, optimize behaviors, increase sales and employee performance, improve margins, increase operational efficiencies, mitigate risk, design better incentive compensation plans, and reduce error rates in incentive compensation calculations.

We were the first 100% cloud-based, multi-tenant provider focusing solely on the incentive compensation and employee and sales performance management market, and we achieved our leadership position through domain expertise and innovative technology. We deliver our solutions through a Software-as-a-Service (SaaS) business model.

Xactly is proud to be an Equal Opportunity Employer. Xactly provides equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, pregnancy, sexual orientation, or any other characteristic protected by law. This means we believe in celebrating diversity and creating an inclusive workplace environment, where everyone feels valued, heard, and has a sense of belonging. By doing this, everyone in the Xactly family has the power to make a difference and unleash their full potential.

THE OPPORTUNITY

As an Associate Quality Engineer at Xactly, you will be responsible for quality assurance related activities and following the complete end-to-end testing lifecycle including testing the products existing and new features, automating test cases, reporting bugs, etc. You will be trained well on all aspects i.e. Products training, Automation tools & infrastructure, CI/CD etc. ensuring their success in scrum teams. Xactly QE team members work with the cutting edge tools & technologies like Selenium Webdriver, Java, TestNG, Maven, RestAssure, Nightwatch, VMWare, Jenkins, Docker, OpenNebula, Jmeter to name a few.

THE TEAM

Xactly's QE team is a rapidly growing & very well diversified team with very strong focus on cutting-edge test automation tools & technologies. We are a very strong team comprising of 35+ members spread across our engineering centers in San Jose, Denver and Bangalore (India). All engineers in QE team are encouraged to operate independently and with highest levels of accountability. Each QE engineer works with tight-knit team of back-end developers, front-end developers, Product Managers in the scrum teams with laser focus on producing high quality code & products for our customers.

THE SKILL SET

• Bachelor&aposs degree in Computer Science or related field is preferred
• 0-2 years of experience in a QA or testing environment
• Ability to develop test strategy, design test plans and test cases
• Experience in an Agile Scrum methodology
• Programming experience in one OOP language such as Java
• Strong SQL query knowledge
  
  

Within One Month, You'll

• Attend New Hire Training
• Learn the Dev and QE processes
• Gain exposure to Xactly QE tools & technologies
• Participate in scrum development process
• Get to know your team
  
  

Within Three Months, You'll

• Learn Xactly's SaaS technology stack
• Learn the Xactly product & feature suite
• Learn Xactly QE automation frameworks, tools & technologies
• Participate in QE activities like test planning & automations in scrum teams
  
  

Within Six Months, You'll

• Ensure best QE practices are being used
• Ensure that we are releasing high quality releases
• Participate & contribute towards Product & feature releases
• Perform RCA's on Production Escapes and ensure corrective actions are implemented.
  
  

Within Twelve Months, You'll

• Gain expertise in Xactly product you are working on
• Take full ownership of features/modules you are responsible for testing.
• Work closely with your scrum teams is sprint planning & feature design discussions
• Continuously work on process improvements in your team to minimize production defect escapes
  
  

Benefits & Perks

• Paid Time Off (PTO)
• Comprehensive Health and Accidental Insurance Coverage
• Tuition Reimbursement
• XactlyFit Gym/Fitness Program Reimbursement
• Free snacks onsite(if you work in office)
• Generous Employee Referral Program
• Free Parking and Subsidized Bus Pass (a go-green initiative!)
• Wellness program
  
  

OUR VISION

Unleashing human potential to maximize company performance. We address a critical business need: to incentivize employees and align their behaviors with company goals.

OUR CORE VALUES

Customer Focus | Accountability | Respect | Excellence (CARE) are the keys to our success, and each day we're committed to upholding them by delivering the best we can to our customers.

Xactly is proud to be an Equal Opportunity Employer. Xactly provides equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, pregnancy, sexual orientation, or any other characteristic protected by law. This means we believe in celebrating diversity and creating an inclusive workplace environment, where everyone feels valued, heard, and has a sense of belonging. By doing this, everyone in the Xactly family has the power to make a difference and unleash their full potential.

Skills Required
Java, Maven, Sql, TestNG, Jenkins, VMware, Docker, Jmeter, Selenium Webdriver

**Join Amgen's Mission of Serving Patients**
At 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.
Project Management Coordinator-Documentation Management
**What you will do**
Let's do this. Let's change the world. In this vital role you will the Project Management Coordinator will play a key role for the management of Research & Documents controlled documents through helping to strengthen and advance Amgen's R&D Quality Management System. This role contributes to implementing strategies and to ensure excellence in R&D controlled document management.
**Roles & Responsibilities:**
As an integral team member working globally with R&D Quality team members and R&D Business Process Owners to ensure compliance with GCP regulations and other requirements:
+ Provide technical writing and editing expertise to support the generation of robust, well-written R&D controlled documents.
+ Coordinate workflows for R&D documents (e.g., SOPs) in controlled document management system.
+ Oversee workflow completion, updates, tracking status, and follow-up activities.
+ Perform Quality Checks and editing against R&D templates.
+ Assist PM/Quality Lead with writing support during project meetings.
+ Follow step-by-step instructions and perform repetitive tasks accurately
+ Communicate and educate clients on R&D document processes, troubleshooting issues, and resolving complaints
+ Supports Amgen's procedural framework so that all procedures maintain compliance to relevant laws, regulations, and internal quality standards; works to ensure that procedures maintain the ethical and safe treatment of all research subjects and that all data has integrity.
+ Coordinate workflows for R&D documents (e.g., SOPs) in controlled document management system
+ Ensures that all procedures are written clearly for the execution of Amgen's GCP/GPvP/GLP research regulations within a diverse, complex, and cross-functional team of researchers.
+ Supports the change control of business procedures in a timely manner with a focus on detail and the output of concisely written documentation.
+ Supports incoming procedural change requests, including the assessment of changes (impact to the QMS, including traceability of changes across other document sets.
+ Applies industry standard methodologies for optimal (standardized and lean) procedural documentation, and the use of technology to drive an efficient and effective GCP/GPvP/GLP quality management system
**What we expect of you**
**Basic Qualifications and Experience:**
+ Master's degree and 1-3 years in Pharma and Biotechnology R&D Quality OR
+ Bachelor's degree and 3-5 years in Pharma and Biotechnology R&D Quality.
**Functional Skills:**
**Must-Have Skills:**
+ Exceptional attention to detail and accuracy in all deliverables.
+ Ability to work independently and proactively in a fast-paced environment.
+ Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and virtual collaboration tools (e.g., Teams, WebEx)
+ Solid understanding of SOP/Standards management, and methods/ technology used to drive knowledge management across a diverse R&D environment.
+ Complex document management in the R&D space with experience in GCP regulations.
+ Effective communication, critical thinking and problem-solving
**Good-to-Have Skills:**
+ Familiarity with project management tools and methodologies.
+ Knowledge of GCP, GLP and/or GPvP.
+ Experience working in a multinational environment with global teams.
+ Experience within Biotech/pharmaceutical Research, including the application of Global Regulations.
+ Direct experience working with standard procedural documentation, including their creation, change control (requests for change and the execution of changes.
+ Independent and team work capabilities
+ Operational and compliance-critical administrative support
**Soft Skills:**
+ Excellent verbal and written communication skills.
+ High degree of professionalism and interpersonal skills.
+ Strong problem-solving abilities and adaptability to changing priorities.
+ Collaborative attitude and ability to build positive relationships across diverse teams.
+ Resilience, discretion, and the ability to thrive under pressure
**Equal opportunity statement**
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.
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.
**What you can expect of us**
As 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.
In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.
**Apply now and make a lasting impact with the Amgen team.**
**careers.amgen.com**
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.

• Having quick turnaround and increased test coverage is the need of the hour; hence the increased emphasis on automation testing across projects. Publicis Sapient is looking for automation experts who in addition to the expertise in the tools and techniques also have the knack to understand the business needs, ROI and accordingly create the automation strategy.
• Assures consistent quality of Software Applications production by developing and enforcing robust Automated Software QE strategy, practices, and processes, providing documentation and managing people. They collaborate the with the project, business and (QE) teams, to develop detailed automated scripts, test frameworks to make the overall system more effective and efficient for our clients.
• Responsible for the overall quality of the project through effective QE leadership and management to ensure that all deliverables in terms of time, price and quality are met. This individual must have a proven track record of success building, leading, and managing a functional and technical QE team with a strong sense of quality ownership.
• This is a hands-on job that requires strategic thinking and planning to provide leadership and expertise throughout the entire QA lifecycle, ensuring the success of the team s manual and automation efforts in an agile working environment
• Able to estimate for low and medium complexity applications and have used at least one of the estimation techniques. Able to handle/oversight a small team ranging from 2 -5 people and can guide them during the complete SDLC cycle starting from test case creation till test closure activities
• Well-versed with most of the activities in defect management process, can define/enhance the defect documentation and TAR lifecycle process independently
• Have expertise to enforce/adhere defect or other processes in the team Preferred (Mostly for people being hired at the Senior Associate Career Stage)
• Mentored or coached at least one person. Can define Automation Test strategy and test plan for low and medium complexity applications taking into account the business needs, ROI etc.
• Able to maintain and report test coverage matrix • Able to identify device coverage for the application in question. Can devise regression testing approach

Qualifications

• 6-9 years of experience with QE for distributed, highly scalable systems.
• Good understanding of OOPS concepts and strong programming skills in Java, Groovy, or JavaScript
• Hands-on experience in working with at least one GUI-based test automation tool for desktop and/or mobile automation. Experience with multiple tools will be added advantage
• Proficient in writing SQL queries & familiarity with the process of test automation tool selection & test approach. Experience in designing and developing automation frameworks and creation of scripts using best industry practices such as Page object model
• Integrate test suites into the test management system and custom test harness. Familiar with the implementation of design patterns, modularization, and user libraries for framework creation
• Can mentor team as well as has short learning curve for new technology, Understands all aspects of Quality Engineering. Understanding of SOAP and REST principles
• Thorough understanding of microservices architecture. In-depth hands-on experience of working with at least one API testing tool like RestAssured, SOAP UI, NodeJS
• Hands-on experience working with Postman or similar tool & parsing complex JSON & XML and data validation using serialization techniques like POJO classes or similar
• Hands-on experience in performing Request and Response Schema validation, Response codes, and exceptions. Good Understanding of BDD, TDD methodologies, and tools like Cucumber, TestNG, Junit, or similar.
• Experience in defining API E2E testing strategy, designing and developing API automation framework. Working experience on building tools Maven / Gradle, Git, etc.
• Experience in creating test pipeline – CI/CD, possess domain knowledge to identify issues across those domains, understand their impact, and drive resolution ((familiar/expert in domains like retail banking, automobile, insurance, betting, food markets, hotel industry, healthcare)
• Used /Exposure to automation tool for automating mobile applications & non-functional testing
• To set up test environment for execution on cloud environments such as Sauce Labs, browser stack. Knowledge of new tools (open source & licensed) in the automation world and have the knack to explore them and keep abreast with the latest tools in the market
• Expertise in creating test automation frameworks, implementing and maintaining them on a project Experience in the modern agile practices such as BDD/Cucumber, DevOps
• Knowledge and experience in service virtualization and tools like CA Lisa. Hands-on knowledge of setting up PACT Broker and writing PACT tests is desirable
• Experience in test management tools like Xray & Zephyr and integration of test framework with these tools. Understanding of commonly used software design patterns like Builder, Factory, Singleton and Façade
• Possess excellent Communication skills (written, verbal both formal & informal). Helps to create a positive, collaborative working environment for the team.
• Quick grasping and flexibility to adapt to new technologies/processes & Ability to multi-task under pressure and work independently with minimal supervision. i.e. Ability to prioritize when under pressure
• Efficiently makes tough decisions and communicates them effectively & independently manages operational level client meetings. Develops strong relationships with appropriate client stakeholders. Acts as the primary POC/facilitator for planned (regular) client meetings. Manages peer-level client relationships (expectations, communications, negotiations, escalation, feedback, etc.)

Education: Full time Bachelor's/Master's engineering degree

Additional Information

Additional information:

• Gender-Neutral Policy
• 18 paid holidays throughout the year 
• Generous parental leave and new parent transition program
• Flexible work arrangements

Employee Assistance Programs to help you in wellness and well being

Company Description

Publicis Sapient is a digital transformation partner helping established organizations get to their future, digitally enabled state, both in the way they work and the way they serve their customers. We help unlock value through a start-up mindset and modern methods, fusing strategy, consulting and customer experience with agile engineering and problem-solving creativity. United by our core values and our purpose of helping people thrive in the brave pursuit of next, our 20,000+ people in 53 offices around the world combine experience across truly value.

Skills Required
Java, Javascript, Groovy

Gaming:

Welcome to the world of land-based gaming. At Light & Wonder, it's all about the games, and our Gaming team builds cutting-edge technology, products, and content for the most iconic casinos and operators across the globe.

Position Summary

JOB DESCRIPTION

Essential Job Functions:

• Ensure that all software is working as intended through rigorous, detailed testing.
• Be the first line of defense in discovering and identifying functionality issues in the game.
• Responsible and accountable for QA sign offs to production.
• Use familiarity with standard QA processes to review bugs, test cases, and create documentation.
• Develop, maintain, and execute test plans and test scripts for existing game themes and features.
• Document, maintain, and track the status of all issues in the bug tracking database (JIRA) until issues are resolved.
• Verify the accuracy of Live Game events, to ensure they match design and have proper functionality.
• Utilize debug, admin, and external software tools to diagnose, reproduce and identify issues.
• Reproduce issues, when necessary, in order to assist software development in resolving issues.
• Generate status reports, documentation, and other low-level reports for supervisors.
• Quickly switch priority, with little downtime.
  
  

Qualifications

Required Qualifications

Education:

• Degree in Computer Science or related field or equivalent relevant experience

Skills Required
Test Plans, Test Scripts, Qa Processes, Jira