288 Quality Assurance Measures jobs in Hyderabad
QA Specialist
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• Bachelor's degree in an IT-related field or equivalent work experience
• Ability to communicate with the company in business language and with developers in technical language and act as a bridge between them.
• In-depth understanding of the Software Development Life Cycle processes with an emphasis on testing methodologies. Must have in-depth Knowledge of system testing techniques.
• Thorough understanding of the end-to-end business process(s) and flows involved in the system capabilities being tested from the system's under test and end to end.
Data QA Specialist
Posted 9 days ago
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About Us:
YipitData is the market-leading data and analytics firm. We analyze billions of data points every day to provide accurate, detailed insights across industries, including consumer brands, technology, software, and healthcare.
Our insights team uses proprietary technology to identify, license, clean, and analyze the data that many of the worlds largest investment funds and corporations depend on. We raised $475M from The Carlyle Group at a valuation over $B, further accelerating our growth and market impact.
We have been recognized multiple times as one of Incs Best Workplaces. As a fast-growing company backed by The Carlyle Group and Norwest Venture Partners, YipitData is driven by a people-first culture rooted in mastery, ownership, and transparency.
With offices in New York, Austin, Miami, Denver, Mountain View, Seattle, Hong Kong, Shanghai, Beijing, Guangzhou, and Singapore, we continue to expand our reach and impact across global markets.
About the Role:
Our newest product offers insights on software companies and is growing rapidly. We are seeking a Financial Analyst (Internal Title: Data QA Specialist) to join our Data Product team in India to manage a large portion of the data cleaning and quality assurance processes for this new product. The Data QA Specialist will be responsible for manually reviewing large datasets of raw financial transaction spend data and helping us transform it into accurate business expense insights. You will verify and make corrections to financial transaction data based on U.S. accounting rules, and youll complete your work primarily using tabular data in our proprietary software. This cleaned data will then be used to build insights products in our fastest-growing initiatives. This position offers the opportunity to meaningfully contribute to the growth of our company. Exceptional employees may have the opportunity to be promoted and manage a team of other Data QA Specialists.
This is a fully remote role based in India.
In general, we expect some overlap with U.S. work hours, and we require greater flexibility (i.e., more overlap) during the first few weeks of training and onboarding. More details on work-hour expectations will be shared during the recruiting process.
We expect hires to start in the position on March 10th, 2025.
As Our Data QA Specialist, You Will:
- Own manually reviewing and updating raw financial transaction spend data and invoices to help transform it into an accurate representation of business expense insights
- Verify and make corrections to financial transaction data following U.S. accounting rules, which will include manually adjusting data by:
- Thoroughly reviewing expense trends over time, across many vendors and different accounting record types
- Deduplicating overlapping transactions such as vendor bill and journal entries and selecting the correct record
- Adjusting amortization dates of expenses
- Inferring amortization dates of expenses, if they are not clear
- Verifying and tagging the correct vendor for each transaction
- Document repeated data issues and work with other Data and Engineering teams to improve our data quality assurance processes
- Primarily complete your work using Google Sheets and our proprietary software
- Collaborate closely with our U.S.-based Data Product team every day
- Have the opportunity to be promoted to manage a team of other Data QA Specialists
You Are Likely to Succeed If:
- You have 0 to 3 years of experience as a data or quality assurance analyst
- You have at least 1 year of full-time work experience as an A/P bookkeeper, junior accountant, Accounts Payables (A/P) clerk, or in a similar position using U.S. accounting practices
- You have experience with Netsuite, Sage, Quickbooks, Xero (or similar ERP software)
- You have exceptional attention to detail
- You have experience working with large datasets
- You have experience managing multiple processes in parallel
- You like to solve problems and puzzles
- You have excellent written and verbal communication skills, with the ability to interact effectively with vendors and internal teams across time zones and cultures
What We Offer:
Our compensation package includes comprehensive benefits, perks, and a competitive salary:
We care about your personal life and we mean it. We offer flexible vacation, parental leave, team events, learning reimbursement, and more!
Your growth at YipitData is determined by the impact that you are making, not by tenure, unnecessary facetime, or office politics. Everyone at YipitData is empowered to learn, self-improve, and master their skills in an environment focused on ownership, respect, and trust.
The annual salary for this position is anticipated to be 10,000 - 15,000 (USD). The final offer may be determined by a number of factors, including, but not limited to, the applicant's experience, knowledge, skills, and abilities, as well as internal team benchmarks.
We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, marital status, disability, gender, gender identity or expression, or veteran status. We are proud to be an equal opportunity employer.
RCM QA Specialist
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We are united in our mission to make a positive impact on healthcare. Join Us!
Who we are:
We Are Modernizing Medicine (WAMM)! We’re a team of bright, passionate, and positive problem-solvers on a mission to place doctors and patients at the center of care through an intelligent, specialty-specific cloud platform. Our vision is a world where the software we build increases medical practice success and improves patient outcomes. Founded in 2010 by Daniel Cane and Dr. Michael Sherling, we have grown to over 3400 combined direct and contingent team members serving eleven specialties, and we are just getting started! ModMed's global headquarters is based in Boca Raton, FL, with a growing office in Hyderabad, India, and a robust remote workforce across the US, Chile, and Germany.
The RCM Quality Assurance (QA) Specialist will be responsible for auditing the work of RCM analysts to ensure the highest standards of services are delivered. They will play a pivotal role in identifying process gaps and work closely with onshore and offshore teams to define SOPs and decision trees that will improve the process.
The Role:
Skills & Requirements:
ModMed Benefits Highlight: At ModMed, we believe it’s important to offer a competitive benefits package designed to meet the diverse needs of our growing workforce. Eligible Modernizers can enroll in a wide range of benefits:
India
United States
PHISHING SCAM WARNING: ModMed is among several companies recently made aware of a phishing scam involving imposters posing as hiring managers recruiting via email, text and social media. The imposters are creating misleading email accounts, conducting remote "interviews," and making fake job offers in order to collect personal and financial information from unsuspecting individuals. Please be aware that no job offers will be made from ModMed without a formal interview process, and valid communications from our hiring team will come from our employees with a ModMed email address (). Please check senders’ email addresses carefully. Additionally, ModMed will not ask you to purchase equipment or supplies as part of your onboarding process. If you are receiving communications as described above, please report them to the FTC website.
QA Specialist - Manual
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Tech Firefly is teaming up with an American multinational tech company that specializes in Internet services and products. This is a great opportunity for motivated candidates to use their Software Quality Assurance skills for one of the biggest companies in the world.
We are looking for someone who will specialize in manually testing the web applications. The main focus will be on providing clear and actionable feedback on UI, UX, and responsive design across a variety of platforms (Email Clients and Web Browsers) and languages. QA Specialist will focus on manually testing existing test cases and creating bugs for content creators.
Hiring Immediately
- Experience: 2 to 3 years only
Requirements
- Bachelor’s degree (technical concentration preferable)
- 1 to 2 years of Manual QA experience
- Experience in operating within and leading cross-functional teams (e.g. engineering, product management, sales, implementation)
- Enjoys working autonomously as well as collaboratively.
Preferred Qualifications:
- Experience in Learning Management systems and Web Accessibility
- Superior problem solving and analytical skills
- Excellent relationship building, collaboration, strong communication, project management and analytical skills required
- Able to succeed despite high levels of ambiguity
- Capable of speaking to both technical and business stakeholders and users
Benefits
- American Work Culture & Project Exposure
- Experience working with one of the best IT companies in the world
Salesforce FSL QA Specialist
Posted today
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Roles & Responsibilities
Qualifications
Experience: 7+ Years
Location: Hyderabad
Working mode: Hybrid, 3 days in a week
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QA Lead Specialist
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We are seeking an experienced Quality Assurance Consultant to oversee quality checks for product batches before export. This role involves close coordination with accredited labs, suppliers and internal teams to ensure compliance with quality standards and regulatory requirements.
Key Responsibilities:
- Coordinate with NABL-accredited laboratories for COA, HPTLC, heavy metals and microbial testing.
- Review supplier GMP compliance, batch manufacturing records and packaging quality.
- Maintain and update QA checklists for each batch.
- Approve and release batches for shipment after quality clearance.
- Provide ongoing support for audits and export documentation as needed.
Requirements:
- Minimum 4+ years of experience in Quality Assurance within pharma, Ayurveda or related industries.
- Strong knowledge of COA interpretation, testing methodologies and lab coordination.
- Familiarity with GMP standards and export QA processes.
- Ability to coordinate remotely with suppliers, labs and regulatory bodies.
Our Ideal Candidate
- The ideal candidate will have a proven track record of ensuring quality standards are met across multiple locations.
- A strong analytical mindset with excellent problem-solving skills is essential for this role.
About the Role
This is a fantastic opportunity for a talented professional looking to make a real impact in our organization. If you are passionate about delivering high-quality products and services, we encourage you to apply.
Specialist QA

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**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 Specialist QA plays a critical role in supporting product disposition related tasks across the Amgen Quality Operations Network. The Specialist QA will leverage industry, technical, and quality systems knowledge to provide support of product expiry management processes, product complaints processes, disposition manager training, and fulfillment of disposition related data requests 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 globally.
**Key Responsibilities**
**DSI/DS/DP material shelf-life extension**
- Executing the GMP process to extend expiration dates for clinical and commercial products produced at Amgen.
- Updating batch product expiration dates in the Amgen SAP inventory management system.
- Evaluating (approve or reject) expiry-SAF forms (expiry stability assessment forms).
**Disposition Support of Partner Requests**
- Support requests made by Amgen partners for data and information related to their partnered product batches manufactured at Amgen sites.
- Data recovery from systems including, but not limited to, manufacturing execution system electronic batch records, the quality control laboratory information system, the regulatory information management system, and the Amgen enterprise resource management system (SAP).
- Uploading and communication of collected data to Amgen partners.
**COA Generation, special requests after disposition**
- Generation and provision of Certificate of Analysis (CofA) records for Amgen drug substance, drug product, or final drug product batches.
- Uploading and communication of collected documentation to requestor (i.e. Amgen partners, regulatory compliance to support RTQs, process development).
**Disposition Manager Training**
- Execution and delivery of quality systems training to new disposition managers across the Amgen network via virtual meetings.
- Training subject matter to include use of quality systems applied to execute the disposition process (i.e. ERP/SAP, MES/EBR, ARRS, LIMS, TW, CDOCS, DQMS, Kneat, etc.)
- Maintenance and revision of training document materials in the controlled documents management system (CDOCs).
**Product Complaints**
- Execution of the drug substance, drug product, and final drug product complaint full batch record review process.
- Assessing electronic batch record (EBRs) documentation in the manufacturing execution system (MES) to identify any potential issues relevant to the complaint.
- Recording the results of the complaints batch record assessment in the Bioconnect quality system.
**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.
- Excellent verbal and written communication skills
- Proven ability to lead and collaborate within cross-functional teams in a dynamic, fast-paced setting.
- Experience in manufacturing environments
**Core Competencies**
- 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 (QMTS), deviation (DQMS), and quality control laboratory information management systems (LIMS).
-Experienced in staff training and development.
- Technical Document Drafting and Workflow Ownership
Basic Qualifications and Experience:
- Master's degree with 8-12 years of Pharma and Biotech commercial or clinical manufacturing Quality experience.
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Quality Control Engineer
Posted 9 days ago
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Key Responsibilities:
- Develop, implement, and maintain quality control plans and procedures.
- Conduct inspections and tests on materials, components, and finished products.
- Analyze quality data and identify trends, defects, and areas for improvement.
- Perform root cause analysis for quality issues and implement effective corrective and preventive actions (CAPA).
- Collaborate with production and engineering teams to resolve quality-related problems.
- Ensure compliance with industry standards, regulatory requirements, and customer specifications.
- Manage supplier quality, including audits and performance evaluations.
- Develop and maintain quality documentation, including test reports and quality manuals.
- Participate in internal and external audits of the quality management system.
- Promote a culture of quality and continuous improvement throughout the organization.
Qualifications:
- Bachelor's degree in Engineering (Mechanical, Electrical, or related field) or a relevant technical discipline.
- 3-5 years of experience in quality control or quality assurance within a manufacturing environment.
- Strong knowledge of quality management systems (e.g., ISO 9001) and statistical process control (SPC).
- Experience with root cause analysis tools and techniques (e.g., 5 Whys, Fishbone diagrams).
- Proficiency in interpreting technical drawings, specifications, and test methods.
- Excellent analytical, problem-solving, and organizational skills.
- Strong communication and interpersonal skills to effectively collaborate with teams.
- Detail-oriented with a commitment to accuracy.
- Experience with metrology and calibration procedures is a plus.
Senior Manager Quality Control

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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.
**ABOUT THE ROLE**
**Role Description:**
In this vital role, you will lead the Amgen India, Quality Control Technical Resources Team. This is a unique opportunity to support the global Quality Control network and to learn about the testing of Amgen products through various stages of the product lifecycle. In addition, as this is a newly formed team, the Senior Manager will have the opportunity to develop new business processes and to strategically develop the team structure.
The QC Technical Resources team will primarily provide centralized document management support for the global QC Network. This will include the creation and/or revision of controlled documents within Amgen's enterprise document management system for a variety of QC processes. The Senior Manager Quality Control will provide management oversight of this team while fostering a culture of innovation, quality and collaboration. The Senior Manager will report directly to Amgen India Quality Leadership.
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 globally.
**Roles & Responsibilities:**
The Senior Manager Quality Control will be accountable for the following activities:
- Daily management of the Quality Control Technical Resources team
- Responsible for organizing team resources to ensure that agreed upon due dates are met for QC Network requests
- Responsible for creating and maintaining business processes and tools that will facilitate the management and visibility of QC network requests
- Responsible for ensuring that the Technical Resources team has access to the required laboratory information management and enterprise systems needed to carry out document management tasks (for example, LIMS, electronic laboratory notebook).
- Responsible for leading issue resolution and problem-solving exercises within the team and cross-functionally, as needed
- Support staff training, career development and performance management
- Responsible for ensuring compliance with safety guidelines, cGMPs and other applicable regulatory requirements.
**Additional Responsibilities:**
- Participate in Amgen global network teams
- Establish and enable LEAN principles across area of responsibility
- Establish and enable department goals, strategies and KPIs
- Champion site and QC global process improvements
- Interfaces with management on significant matters, often requiring the coordination of activity across organizational units
- Plans and organizes project assignments of substantial variety and complexity
- Translates complex data into actionable information and applies strong technical knowledge to meet business objectives
- Identifies process gaps, introduces innovative solutions, and leads operational excellence projects to improve efficiency and productivity, while decreasing expense/operating costs.
- Leads root cause analysis discussions for more complex problems to develop and efficiently implement effective permanent solutions.
**Basic Qualifications and Experience:**
+ Master's degree with 12-16 years of Pharma and Biotech commercial or clinical manufacturing Quality Control experience
AND
+ 5 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources
**Functional Skills:**
**Must-Have Skills:**
+ Experience working and leading teams in a cGMP laboratory environment.
+ Strong technical writing skills within a highly regulated environment.
+ Working knowledge of cGMP regulations, practices, and trends pertaining to Quality Control.
+ Experience managing staff and/or leading teams, projects, programs or directing the allocation of resources.
**Good-to-Have Skills:**
+ Track record of building or participating as a member of high performing team.
+ Experience with various laboratory computer systems and applications.
+ Strong leadership and negotiation skills with a demonstrated ability to influence different styles.
+ Demonstrated innovative thinking and ability to transform work organizations.
+ Exposure to Operational Excellence initiatives.
+ Understanding of quality management systems and quality control processes related to drug substance and drug product for clinical and commercial operations.
+ Demonstrated ability to navigate through ambiguity and provide structured problem solving.
+ Demonstrated ability to coordinate multi-functional project teams and deliver on schedule.
+ Demonstrated ability to coordinate and lead cross-functional teams.
+ Demonstrated ability to find opportunities and implement new technologies and services to transform the business into a more agile, efficient and effective organization.
+ Demonstrated skills in staff motivation, coaching/mentoring and professional development.
+ Great teammate who can collaborate and provide leadership through influence to achieve the required results.
**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.