Explore exciting QA Manager jobs in 325 Qa Manager jobs in Hyderabad
QA Manager
Posted 17 days ago
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Job Description
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.
Amgen 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.
**QA Manager**
**What you will do**
**Role Description:**
In this role you will be serving patients through internal collaboration with Amgen's global quality teams, manufacturing sites and external engagement with contract manufacturing organizations. You will make key contributions to fulfill Amgen's missions of serving patients by ensuring supply of high-quality product produced at contract manufacturers to patients.
The QA Manager will support implementation and management of quality assurance activities at the Amgen Technology and Innovation Center, supporting oversight and maintenance of external suppliers and contract manufacturers. You will be responsible for leading a team of quality professionals who will be maintaining and approving various quality documents including but not limited to: supplier documentation, analytical results investigations, CAPA and audit records. This role will involve collaboration with various Amgen teams to ensure seamless handoffs between teams
**Roles & Responsibilities:**
+ Oversee a team of approx. 6 staff, ensuring their activities and priorities are managed in a compliant and structured manner.
+ Ensure team members are appropriately qualified and trained to perform needed activities per company procedures.
+ Conduct goal setting, performance reviews, and compensation planning to align with organizational goals.
+ Develop, implement, and maintain quality records in compliance with industry standards, GMP practices, and regulatory requirements.
+ Continuously improve processes to enhance efficiency and quality, by applying lean principles and automation.
+ Develop, monitor and report metrics to senior management to assess the health of the team's performance.
+ Develop solutions that are thorough, practical, and consistent with functional objectives.
+ Work cross functionally with various Amgen teams and stakeholders to ensure seamless transition of tasks and continuity across groups.
+ Prepare, review and approve SOPs and other GMP/GDP documentation in compliance with corporate and regulatory requirements, to ensure alignment with procedures, current Good Manufacturing Practices (cGMP), Good Distribution Practices (GDP) and other applicable regulations.
This role may require working in shifts or extended hours within the same shift to support global time zones.
**What we expect of you**
**Basic Qualifications and Experience:**
+ Doctorate degree OR
+ Master's degree with 4 to 6 years of experience in quality management systems or a related field OR
+ Bachelor's degree with 6 to 8 years of experience in quality management systems or a related field OR
+ Diploma with 10 to 12 years of experience in quality management systems or a related field.
+ Experience managing staff in a GXP environment
**Functional Skills:**
**Must-Have Skills:**
+ Working foundation in quality assurance roles and proven team leader.
+ Minimum of 6 years working in a cGMP manufacturing environment with a strong understanding of regulatory requirements and expectations.
+ Ability to have a positive impact on others; the ability to affect the behaviors of others by connecting with and inspiring them
**Good-to-Have Skills:**
+ Experience in investigations, project management and trending and analysis
+ Relevant experience in Supplier Management, raw materials, packaging components, and/or device manufacturing.
+ Understanding of the applicable manufacturing/testing processes (i.e. API, Drug Substance, Drug Product, Packaging, Device manufacturing processes).
+ Proven experience in designing and/or improving processes at conceptual level
+ Desire to partner with internal and external stakeholders across teams
+ Understanding of industry requirements/expectations of a robust Quality Management System and documentation.
**Soft Skills:**
+ Excellent analytical and troubleshooting skills.
+ Strong verbal and written communication skills
+ Ability to work effectively with global, virtual teams
+ High degree of initiative and self-motivation.
+ Ability to manage multiple priorities successfully.
+ Team-oriented, with a focus on achieving team goals
+ Strong presentation and public speaking skills.
**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.
**Apply now**
for a career that defies imagination
Objects in your future are closer than they appear. Join us.
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.
QA Manager
Posted today
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Job Description
QA Manager
Description:
Zeta Global is looking for a QA Manager who is self-motivated, creative, with an outgoing and proactive approach to management. You will work with our business partners to establish viable and reusable use cases as we onboard and maintain clients on the Zeta Marketing Platform.
The selected candidate will excel in a fast-paced environment, being able to manage multiple priorities and deliverables in a given day. You will provide hands-on support and expertise in learning and understanding our products and their domains.
You will work closely with various stakeholders throughout the development lifecycle, executing automated test cases, tracking, and reporting test results, troubleshooting and coordinating bug fixes. You will have a strong understanding of testing methodologies and have the ability to implement best practices.
Responsibilities:
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Lead and manage a team of QA professionals across the globe, including manual testers and automation engineers.
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Actively collaborate with cross functional teams including Business System Analysts, Developers, Project/Deliver Mgmt. Teams, and Product Managers to ensure quality throughout the development lifecycle.
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Embed the QA team early on in projects where we can work hand in hand with the BSA team during the data discovery process to build out well executed use cases.
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Provide feedback to the team on product quality, call out risks/issues, and balance quality with time bound delivery with a release perspective.
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Document and maintain manual as well as automated test result.
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Understand the product domain, understand the vision, roadmap, and team goals of the product.
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Identify opportunities for process improvement and implement solutions to enhance product quality and team efficiency.
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Design and develop robust automation frameworks and manage the execution of automated and manual tests.
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Establish and evolve formal QA processes, ensuring that the team is using best practices.
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Maintain detailed testing documentation related to the software or system.
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Leverage new technologies (AI) to expand testing accuracy and velocity on projects.
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Implementation, monitoring, and reporting on QA KPIs.
Qualifications:
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Bachelor's degree in computer science, Engineering, or a related field (or equivalent experience).
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Minimum of 5 years of management experience, overseeing at least 5 direct reports.
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Strong experience in coaching and developing team members to support their career growth.
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Proven ability to work collaboratively with cross-functional teams to identify and resolve issues.
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Hands-on experience with manual testing, as well as the design and development of automation frameworks.
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Strong problem-solving and analytical skills.
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Strong written and spoken English communication skills.
Skills and Competencies:
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Proficiency in testing frameworks, such as Robot, Selenium, TestRail, Python with PyCharm IDE.
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ETL – Strong understanding of transforming complex data sets as well as working with various data sets, including delimited, XML, and JSON.
• Database - Hands on experience with the following database Technologies.
Snowflake (Required)
MYSQL/PostgreSQL – Nice to have
iliar with NOSQL DB methodologies (Nice to have)
• Programming Languages – Can demonstrate knowledge of any of the following.
PL Strong Plus
avaScript Strong Plus
ython - Strong Plus
• AWS – Knowledge of the following AWS services:
S3 />•
Experience with MarTech including, email, SMS, CDM (customer data management).
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Experience with AI Agents to assist with data observability and governance is a plus.
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Jira for Bug and Time tracking.
Company Summary:
Zeta Global is a NYSE listed data-powered marketing technology company with a heritage of innovation and industry leadership. Founded in 2007 by entrepreneur David A. Steinberg and John Sculley, former CEO of Apple Inc and Pepsi-Cola, the Company combines the industry’s 3rd largest proprietary data set (2.4B+ identities) with Artificial Intelligence to unlock consumer intent, personalize experiences and help our clients drive business growth. Our technology runs on the Zeta Marketing Platform, which powers ‘end to end’ marketing programs for some of the world’s leading brands. With expertise encompassing all digital marketing channels – Email, Display, Social, Search and Mobile – Zeta orchestrates acquisition and engagement programs that deliver results that are scalable, repeatable and sustainable. Zeta Global is an Equal Opportunity/Affirmative Action employer and does not discriminate on the basis of race, gender, ancestry, color, religion, sex, age, marital status, sexual orientation, gender identity, national origin, medical condition, disability, veterans status, or any other basis protected by law.
Zeta Global Recognized in Enterprise Marketing Software and Cross-Channel Campaign Management Reports by Independent Research Firm
QA Specialist / QA Manager (Clinical Quality Assurance)
Posted today
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Job Description
Commitment: Full-Time Contract (30–40 hours per week)
Location: Based in India, Remote – Eastern Time Zone (preferred) or Mountain Time Zone
Reports To: Clinical QA Lead / Director of Quality
Position Overview
We are seeking an experienced QA Specialist / Manager-level contractor to provide day-to-day clinical quality assurance (QA) support across ongoing clinical trials. This individual will play a key role in guiding study teams, maintaining compliance with Good Clinical Practice (GCP) , and ensuring quality oversight. The ideal candidate brings strong experience with Veeva QMS , is highly tech-savvy, and can support clinical operations teams in a fast-paced, remote environment.
Key Responsibilities
- Serve as the primary QA support resource for clinical study teams, ensuring compliance with GCP and internal quality standards.
- Provide QA expertise during study calls, including:
- Protocol deviation meetings
- Risk-based quality management discussions
- Study operations and trial oversight meetings
- Write, review, update, and format standard operating procedures (SOPs) and other quality documentation.
- Manage and track quality processes within Veeva QMS , including document control, training, and CAPA management.
- Address QA-related questions from study teams in real time, providing clear and actionable guidance.
- Support inspection readiness and contribute to continuous improvement of QA systems and processes.
- Partner with cross-functional stakeholders (Clinical Operations, Data Management, Regulatory, etc.) to align on quality expectations and risk mitigation.
Qualifications
- Education: Bachelor’s degree in life sciences, healthcare, or related discipline (advanced degree preferred).
- Experience:
- 5+ years of Clinical Quality Assurance experience with a strong foundation in GCP.
- Prior experience supporting clinical study teams in a QA capacity.
- Hands-on experience with Veeva QMS .
- Technical Skills:
- Proficient in MS Office (Excel, PowerPoint, Word).
- Skilled in technical writing, SOP drafting, and document formatting.
- Soft Skills:
- Excellent communication and interpersonal skills.
- Strong organizational skills with the ability to work independently.
- Availability: Must be available during Eastern or Mountain Time Zone working hours to attend study calls and provide timely QA support.
Contract Opportunity
This is a full-time contract role offering 30–40 hours per week of consistent work. The contractor will act as a core member of the QA function, providing essential support to ongoing clinical programs and ensuring regulatory compliance.
QA Specialist / QA Manager (Clinical Quality Assurance)
Posted 4 days ago
Job Viewed
Job Description
Commitment: Full-Time Contract (30–40 hours per week)
Location: Based in India, Remote – Eastern Time Zone (preferred) or Mountain Time Zone
Reports To: Clinical QA Lead / Director of Quality
Position Overview
We are seeking an experienced QA Specialist / Manager-level contractor to provide day-to-day clinical quality assurance (QA) support across ongoing clinical trials. This individual will play a key role in guiding study teams, maintaining compliance with Good Clinical Practice (GCP) , and ensuring quality oversight. The ideal candidate brings strong experience with Veeva QMS , is highly tech-savvy, and can support clinical operations teams in a fast-paced, remote environment.
Key Responsibilities
- Serve as the primary QA support resource for clinical study teams, ensuring compliance with GCP and internal quality standards.
- Provide QA expertise during study calls, including:
- Protocol deviation meetings
- Risk-based quality management discussions
- Study operations and trial oversight meetings
- Write, review, update, and format standard operating procedures (SOPs) and other quality documentation.
- Manage and track quality processes within Veeva QMS , including document control, training, and CAPA management.
- Address QA-related questions from study teams in real time, providing clear and actionable guidance.
- Support inspection readiness and contribute to continuous improvement of QA systems and processes.
- Partner with cross-functional stakeholders (Clinical Operations, Data Management, Regulatory, etc.) to align on quality expectations and risk mitigation.
Qualifications
- Education: Bachelor’s degree in life sciences, healthcare, or related discipline (advanced degree preferred).
- Experience:
- 5+ years of Clinical Quality Assurance experience with a strong foundation in GCP.
- Prior experience supporting clinical study teams in a QA capacity.
- Hands-on experience with Veeva QMS .
- Technical Skills:
- Proficient in MS Office (Excel, PowerPoint, Word).
- Skilled in technical writing, SOP drafting, and document formatting.
- Soft Skills:
- Excellent communication and interpersonal skills.
- Strong organizational skills with the ability to work independently.
- Availability: Must be available during Eastern or Mountain Time Zone working hours to attend study calls and provide timely QA support.
Contract Opportunity
This is a full-time contract role offering 30–40 hours per week of consistent work. The contractor will act as a core member of the QA function, providing essential support to ongoing clinical programs and ensuring regulatory compliance.
QA Specialist / QA Manager (Clinical Quality Assurance)
Posted 4 days ago
Job Viewed
Job Description
Commitment: Full-Time Contract (30–40 hours per week)
Location: Based in India, Remote – Eastern Time Zone (preferred) or Mountain Time Zone
Reports To: Clinical QA Lead / Director of Quality
Position Overview
We are seeking an experienced QA Specialist / Manager-level contractor to provide day-to-day clinical quality assurance (QA) support across ongoing clinical trials. This individual will play a key role in guiding study teams, maintaining compliance with Good Clinical Practice (GCP) , and ensuring quality oversight. The ideal candidate brings strong experience with Veeva QMS , is highly tech-savvy, and can support clinical operations teams in a fast-paced, remote environment.
Key Responsibilities
- Serve as the primary QA support resource for clinical study teams, ensuring compliance with GCP and internal quality standards.
- Provide QA expertise during study calls, including:
- Protocol deviation meetings
- Risk-based quality management discussions
- Study operations and trial oversight meetings
- Write, review, update, and format standard operating procedures (SOPs) and other quality documentation.
- Manage and track quality processes within Veeva QMS , including document control, training, and CAPA management.
- Address QA-related questions from study teams in real time, providing clear and actionable guidance.
- Support inspection readiness and contribute to continuous improvement of QA systems and processes.
- Partner with cross-functional stakeholders (Clinical Operations, Data Management, Regulatory, etc.) to align on quality expectations and risk mitigation.
Qualifications
- Education: Bachelor’s degree in life sciences, healthcare, or related discipline (advanced degree preferred).
- Experience:
- 5+ years of Clinical Quality Assurance experience with a strong foundation in GCP.
- Prior experience supporting clinical study teams in a QA capacity.
- Hands-on experience with Veeva QMS .
- Technical Skills:
- Proficient in MS Office (Excel, PowerPoint, Word).
- Skilled in technical writing, SOP drafting, and document formatting.
- Soft Skills:
- Excellent communication and interpersonal skills.
- Strong organizational skills with the ability to work independently.
- Availability: Must be available during Eastern or Mountain Time Zone working hours to attend study calls and provide timely QA support.
Contract Opportunity
This is a full-time contract role offering 30–40 hours per week of consistent work. The contractor will act as a core member of the QA function, providing essential support to ongoing clinical programs and ensuring regulatory compliance.
QA / Release Manager
Posted today
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Job Description
Job Description:
We seek a highly skilled and experienced QA / Release Manager to join our team. The ideal candidate will drive the quality and timely release of our products. This role involves defining testing procedures, implementing test automation, and certifying readiness for release to production.
Key Responsibilities:
- Define and implement comprehensive testing procedures.
- Choose and implement test automation tools and strategies.
- Certify and approve software readiness for production releases.
- Ensure all Jira work items include agreed-upon definitions of done (DoD) to ensure proper text coverage.
- Collaborate with the development and product teams to ensure seamless integration and deployment of software releases.
Qualifications:
- Proven experience in software quality assurance and release management.
- Strong knowledge of test automation tools and methodologies.
- Experience with Jira and other project management tools.
- Excellent communication and collaboration skills.
- Ability to work in a fast-paced, dynamic environment.
Preferred Skills:
- Experience with Agile methodologies.
- Experience with the Atlassian Cloud platform.
- Familiarity with continuous integration and continuous deployment (CI/CD) practices.
- Strong problem-solving skills and attention to detail.
Application Process: Interested candidates should submit their resume and a cover letter detailing their experience and qualifications for the role
Manager - QA
Posted today
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Job Description
Genpact (NYSE: G) is a global professional services and solutions firm delivering outcomes that shape the future. Our 125,000+ people across 30+ countries are driven by our innate curiosity, entrepreneurial agility, and desire to create lasting value for clients. Powered by our purpose – the relentless pursuit of a world that works better for people – we serve and transform leading enterprises, including the Fortune Global 500, with our deep business and industry knowledge, digital operations services, and expertise in data, technology, and AI.
Inviting applications for the role of Quality Manager, Trust & Safety
Responsibilities
• Implement a clear overall quality strategy with scalable processes/tools/systems that allow resource efficient monitoring of decision accuracy and surface overall user experience issues fast and effectively to define appropriate continuous improvement programs.
• Liaison with internal and external stakeholders to ensure quality targets are met
• Passionately tell the story of why Quality matters, build consensus, and inspire others to move fast on fixing problems.
• Effectively manage and mentor a team responsible for diverse workflows, Quality channels, and stakeholders
• Drive accountability with team managers and their teams to meet quality performance goals and ensure program standards are met on a week-over-week basis.
• Assess and prioritize the top-quality issues affecting the teams in your office across all decision-making channels.
• Quantify business cases and drive cross-functional partners to change our systems, processes, and policies to achieve better outcomes.
• Drive investigation of highly sensitive issues affecting your office, working with teams and leaders across Client to understand what happened and why.
• Stay connected with how our support ecosystem is evolving and help head off quality issues before they begin, as Client’s products and communities change and grow.
• Find creative workarounds for quality issues where our tools are the root cause, and a technical solution is not imminent.
• As new Quality Measurement Systems are being developed and prototyped, provide details to local teams around the impact of the new change on the team’s current work and surfaces gaps in knowledge.
Qualifications we seek in you.
Minimum qualifications
· Any graduate /Post Graduate degree or equivalent with a solid academic record
· Relevant experience in the BPM/ Service Industry, with good experience in a Training/Quality, Learning & Development role, communication, and customer experience improvement programs.
Preferred qualifications
• Meaningful work Experience in managing quality control/quality analysis organization or leading cross-functional quality improvement projects and teams in a dynamic environment.
• Proven track record of collaborating with cross-functional groups to produce results.
• Demonstrated ability to perform well in a rapidly changing and extremely global team.
• Strong practical experience with Excel (PivotTable, Charts, Statistical functions) is essential.
• Experience with Tableau/Power BI or other similar tools is a plus.
• Excellent communication skills.
• Strong critical thinking and exceptional problem-solving skills.
• Proven track record of breaking down complex process and identifying key pain points to deliver business improvements at the regional or global level.
• Passion for our mission of ensuring a world class support experience for our community.
• Quality certification (e.g., Lean Six Sigma, TQM, etc.) a plus.
• Project management certification (PMP, Prince2, etc.) is a plus.
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Associate Manager - QA
Posted today
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Job Title: Assistant QA Manager About the Role: We are seeking a dedicated and experienced Assistant QA Manager to support our Engineering team.
The ideal candidate will have a strong background in software quality assurance, with proven experience in assisting with QA team management and driving automation initiatives.
The Assistant QA Manager will help lead a team of 4-5 QA engineers and ensure the highest quality standards for our SaaS products. Key Responsibilities: Support the QA Manager in leading, mentoring, and managing a team of 4-5 QA engineers.
Assist in defining and implementing robust QA processes, test strategies, and automation frameworks.
Collaborate with engineering, product management, and customer support teams to ensure seamless product delivery and high-quality releases.
Assist in overseeing the creation and execution of comprehensive test plans, test cases, and test scripts.
Contribute to test automation efforts to improve test coverage and efficiency.
Monitor and track quality assurance metrics, such as defect densities and open defect counts.
Provide regular feedback and career development guidance to team members.
Participate in sprint planning, daily stand-ups, and retrospectives in an Agile environment.
Identify and help mitigate risks related to software quality, ensuring best practices are followed across the engineering team.
Required Skills & Qualifications: Hands on experience in Katalon Studio is a must Bachelor's degree in Computer Science, Engineering, or a related field.
Experience working with SaaS products, understanding the unique challenges and requirements of SaaS environments.
Strong knowledge of manual and automated testing methodologies.
Proficiency in automation tools (e.g., Selenium, Cypress, Appium) and scripting languages (Python, Java, JavaScript, or Ruby).
Experience with CI/CD tools (e.g., Jenkins, GitLab CI, CircleCI) and cloud environments (AWS, Azure, GCP).
Familiarity with test management tools (e.g., TestRail, Zephyr) and bug tracking systems (e.g., Jira, Bugzilla).
Solid understanding of Agile/Scrum methodologies.
Strong problem-solving, analytical, and decision-making skills.
Excellent communication skills, with the ability to convey technical issues effectively.
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Senior Software QA Lead Engineer and Senior Software QA Manager -Power Systems/Industrial Automation
Posted today
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Job Description
About Company
A leading EPC company specializing in the field of power transmission, distribution and solar energy offers integrated solutions and end-to-end services
Education: Engineering Graduate / Postgraduate | Relevant Exp: 7 9 Years | Designation: Senior Software QA Lead Engineer
Education: Engineering Graduate / Postgraduate | Relevant Exp: 10+ years | Designation: Software QA Manager
Education: Engineering Graduate / Postgraduate | Relevant Exp: 15 - 18 years | Designation: Senior Software QA Manager
Work Location : Chennai / Hyderabad / Indore
Total Relevant Experience: 7 18 yrs.
Relevant Skills
Minimum of 2 3 years of experience in Linux & SQL
Experience in developing Test Plans, Test Cases, Test Scripts, Test Scenarios, Testing logs, reports and documents.
Web- based, Desktop and client-server applications.
Selenium with Java or similar frameworks.
Required Knowledge/Skills, Education, And Experience:
Experience in software testing / quality assurance with web- based applications and client-server applications.
Familiarity with Agile Scrum methodology
Hands-on experience in manual API testing
Experience in automation testing using Selenium or similar frameworks.
Solid knowledge of SQL and scripting
Excellent communication (written, verbal and presentation) skills, and advanced problem-solving orientation and decision-making skills.
Working knowledge of the various types of testing, from functional testing to performance and mobile/browser compatibility.
A passion for technology with demonstrated ability to learn quickly.
Understanding of the web/desktop application development cycle and programming techniques and tools
Excellent project and time management skills.
Ability to work independently or with a group.
Ability to participate in working sessions that result in clear technical requirements and technical design while working with technical, non-technical members.
Ability to write Java code for the purposes of testing solution code (e.g., white-box testing).
Mandatory Skills:
Experience in any SCADA, Controllers, or any industrial automation component like RTU, PLC, IED testing
Experience in testing industrial automation protocols like Modbus, DNP3, IEC 101/104, IEC 61850 etc.,
Experience in developing Test Plans, Test Cases, Test Scripts, Test Scenarios, Testing logs, reports and documents.
Domain experience in Energy, Power, Utilities.
Web- based, Desktop and client-server applications
Selenium or similar frameworks
QA Engineer - Assistant Manager
Posted today
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Job Description
:We are looking for a quality engineer who is experienced in functional and automated testing of software systems in enterprise and cloud infrastructures, understands relational databases/SQL, and has familiarity with Agile development methodologies. The job involves the engineer to work as a member of a Front office Trading team and assist in executing the overall quality plan for components managed the scrum team. The engineer will also be expected to help testing any issues coming from implementation, support, and other development teams within Charles River.
Responsibilities:
Preferred qualifications and education: