7,097 Qa Roles jobs in India
Quality Assurance
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Job Description
Qualification:
Bachelors or Masters in Biomedical Engineering and at least 2 years of experience in quality management system for medical device (ISO
Experience and skills
A candidate should have hands on experience on implementing quality
management system ISO 13485.
Candidates must provide details of QMS projects handled.
nowledge of ISO and IEC standards such as ISO 13485, IEC 60601 standards
ualified internal auditor for ISO 13485
nowledge of Indian Medical device rule,2017.
undamental understanding of product development process (for new
product development) which includes knowledge of hardware, software,
mechanical and regulatory development activities amongst others
Roles and responsibilities
anage quality assurance procedure and records.
lan and guide various labs test for innovative medical device.
repare and submit device dossiers to regulatory bodies as per client needs.
lan and conduct internal audits. Participate in the corrective and preventive
action process.
mparting QMS training to new joinee.
dentifying regulatory design input for design team.
dentifying device related risk as per applicable regulatory requirements.
nsuring medical standard compliance - Studying the applicable product
standards for medical devices, analysis of all applicable sections,
documenting the requirements and design aspects based on the study.
Helping and tracking the implementation.
nsure design and test methodologies meets internal and external regulatory
requirements
xcellent understanding of product risk analysis and FMEA processes w.r.t
corresponding medical standards (IEC ,IEC , ISO 14971 etc).
etailed analysis of Software related risks and processes according to IEC
62304
etailed analysis of usability aspects of medical devices according to HFE 75,
IEC 62366, IEC , data security standards etc.
lan clinical trials for innovative medical device and corresponding regulatory
submission related processes and documentation
orking with cross functional teams to ensure compliance to medical
standards and applicable regulatory rules to ensure good quality project
deliverables.
onducting clinical literature search using databases such as PubMed,
and other internet sources to obtain relevant research
papers for the given medical device.
taying updated on recent trends, developments and advances in medical
device standards.
Add on skills
nowhow of FDA, CE and corresponding compliance requirements
xperience in IVD device, combinational medical device
nderstanding the requirements the quality system requirements of
Regulation MDR 2017/745 and IVDR 2017/746
Other skills
trong analytical skills
etail oriented approach to problems
trong reviewing skills
ood communication and presentation skills
ocus on achieving goals and delivering results
ollaborate and create alignment in a team environment
Quality Assurance
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Job Description
- Assist in preparing validation protocols and reports (SAT, FAT, DQ, IQ, OQ, PQ) for equipment/machine and participates in process, test method validation activities.
- Support execution of validation studies in coordination with Quality Control, Production, Purchase team, Engineering teams.
- Assist in revalidation activities during product or process changes.
- Assist in performing QC testing of medical devices including Functional test and Packaging test and Document QC test results
- Assist in preparing and updating the Risk Management File (RMF) in accordance with ISO 14971.
- Support design activities including the preparation of design inputs, design outputs, design verification and validation.
- Contribute to the creation and maintenance of the Design History File (DHF).
Qualification
Bachelor's degree in Engineering, Biomedical Engineering, Life Sciences or related field.
Job Types: Full-time, Permanent, Fresher
Pay: ₹300, ₹350,000.00 per year
Benefits:
- Food provided
- Health insurance
- Leave encashment
- Life insurance
- Paid sick time
- Provident Fund
Work Location: In person
Quality Assurance
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Quality Assurance (QA) Analyst
Location:
Mumbai Metropolitan Region
Department:
Engineering
Employment Type:
Full Time (Remote)
PeopleGrove is seeking a Quality Assurance Analyst to support an agile product development team. This role will collaborate with product managers and engineers to test, iterate, and approve feature releases in a fast-paced and innovative environment. Candidates should have a strong interest in software development, technology, and the testing process as well as exceptional attention to detail and communication skills.
The Quality Assurance Analyst will report into the Product team and work alongside Product, Engineering, and Customer Success to develop innovative products in a fast-paced environment. This position presents the opportunity to work in a cross-functional and business-critical role in a rapidly growing industry.
Application Form:
Click here to apply
Responsibilities
- Testing new features and providing feedback to the product/engineering team.
- Writing and maintaining efficient, thorough test cases.
- Coordinating and managing feature releases with product/engineering.
- Regression and stability testing on the live environment.
- Performing functional, regression, integration, performance, and security testing.
- Assisting the Customer Success team in reproducing and debugging customer-reported issues.
- Learning and mastering the inner workings of a full enterprise product suite.
- Tracking, logging, and verifying defects in bug-tracking systems (e.g., JIRA, Azure DevOps).
- Contributing to test documentation: test plans, strategies, and reports.
- Ensuring compliance with quality standards and best practices.
- Actively participating in regular knowledge transfer sessions to ensure continuous learning and team alignment.
Desired Skills & Experience
- Total years of experience: 2 to 5 years.
- Extremely detail-oriented, logical, and patient.
- Able to think through and map complex systems and translate them into clear test cases.
- Understanding of test design techniques, SDLC, STLC, and Agile methodologies.
- Perform accessibility testing using keyboard-only navigation, screen readers like NVDA, axe, WAVE to identify and address compliance issues.
- Understanding of WCAG guidelines and accessibility best practices.
- A clear and concise communicator, able to work well with a small and cohesive team.
- A technology enthusiast. Excited to work in a fast-paced development environment and eager to work with new technologies.
- Motivated to learn and grow. This position exposes the candidate to all aspects of a successful product, from development through end-user adoption.
- Interested in entrepreneurship and comfortable with risk. Any small, early-stage business faces big challenges and candidates should be prepared to problem-solve on the fly.
- Hands-on experience on Mixpanel to validate user behavior tracking, event accuracy, and data-driven QA insights.
- Hands-on experience in API manual testing (Postman, Swagger, or similar) including functional, boundary, and negative test scenarios.
Exposure to AI-driven QA tools like:
Testim
- Applitools Eyes (visual testing)
- Katalon with AI
- KaneAI
- QASE
ChatGPT/Rovo (assisted test case generation).
Ability to use AI for test case optimization, defect prediction, and self-healing automation scripts.
Nice-to-Have Skills
- Knowledge of performance testing (JMeter).
- Familiarity with security testing basics (OWASP).
- Cloud testing exposure (AWS Device Farm, BrowserStack, Sauce Labs, LambdaTest).
Salary:
2 - 5 a month
At PeopleGrove, we dont just accept difference we celebrate it, we support it, and we thrive on it for the benefit of our employees, our products, and our community. PeopleGrove is proud to be an equal opportunity workplace.
If you need assistance or an accommodation due to a disability, you may contact us at or you may call us
Quality Assurance
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Role & responsibilities
RESPONSIBILITIES: -
To follow the cGMP Rules and regulation.
Documentation Control: maintenance, updation and issuance of documents in compliance with regulatory requirements and implementation of Good Documentation Practices.
Review and approval of all Master documents like SOP, Batch Manufacturing record, Batch packing record, Calibration schedule, Preventive maintenance Schedule and other quality related documents
Responsible for preparation and review of protocol and report for Process validation, Cleaning validation as per the schedule and validation master plan.
Handling of documents like SOPs, formats / Annexures, Log Books, BMR / BPR & all other GMP Documents like Change control, deviation, incident, CAPA, breakdown slips etc
Responsible for preparation, review and approval of DQ, IQ, OQ and PQ documents for new equipment or existing equipment
Responsible for handling of change controls & implementation of changes.
Responsible for review of all batch related documentation, to support Quality Head to release the product, to support and maintain Environmental Health and Safety requirements as applicable.
To perform & review of risk assessments.
Review & signing of Finished Product data & Certificate of Analysis & product release certificate.
Responsible for review & signing of product stability data
Responsible for preparation/execution of Self Inspection.
Responsible for Annual product quality review reports.
Responsible for handling & maintenance of control / retain samples.
Responsible for review & updation of Batch Manufacturing / Packing records & its issuance.
Responsible for review, updation & maintenance of Master Formula Records.
To plan and execute employees training about departmental SOPs.
Responsible for review the SOPs of Quality Assurance department.
To review of product stability data, Control and retain sample evaluation record
To review & approve all the specifications & standard testing procedure
Responsible for Implementation & to check effectiveness of all regulatory requirements.
To support regulatory department related to documentation & dossier submission activities and to resolve the received technical queries.
Responsible for review & approval of artworks
To review & approve shade cards.
Responsible for review & approval of Bill of Materials.
Execution and review of Aseptic process simulation study
To support IPQA head / team as and when required
To support Validation / Qualification head / team as and when required
To check the effectiveness of GEP (Good engineering practices) at service floor, HVAC system, water system, Nitrogen system and Compressed air system.
Review of APQR
Responsible to inform any Non- Conformity observed in area to Head of the Department
Approve or rejecting starting materials, packing materials, intermediate and bulk roducts in relation to their specifications & batch release.
To prepare/approve risk assessment documents.
To participate in external audit.
Handling of recall.
To approve and monitor analyses carried out under contract.
To ensure maintenance of department, premises and equipment.
To ensure appropriate validations including those of analytical procedures and calibrations of control equipment are carried out.
To ensure training of personnel is carried out.
To approve/authorize personnel of all department.
To approve gowning qualification of personnel.
To ensure/ maintain archival system of documents.
Any assignment other than above responsibility given by reporting authority.
Maintenance of Job responsibilities, Organograms & Specimen signature logs
Preferred candidate profile
Majorly who Have experience in Injectable and Team Handling
Quality Assurance
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Job Title: Quality Assurance Executive Essential Oils
Company: Aromaaz International Pvt. Ltd.
Location: (Ghaziabad)
Job Type: Full-time
Key Responsibilities:
1-Ensure quality of essential oils, absolutes, carrier oils, and related natural products in compliance with international standards.
2-Conduct physical, chemical, and sensory evaluation of raw materials and finished goods.
3-Maintain GC-MS (Gas Chromatography-Mass Spectrometry) and other analytical reports for quality verification.
4-Develop, implement, and monitor SOPs for quality control and assurance across production and packaging units.
5-Coordinate with suppliers and vendors to ensure raw material quality.
6-Ensure adherence to export regulations, safety standards, and certifications (ISO, GMP, HACCP, FSSAI, etc.).
7-Handle documentation, quality reports, COA (Certificate of Analysis), and batch records.
Support R&D and production teams in resolving quality-related issues.
Requirements:
1-Bachelors/Master's degree in Chemistry, Food Technology, Essential Oils, or related field.
2- 1–3 years of experience in Quality Assurance/Quality Control, preferably in essential oils, fragrances, or FMCG export industry.
3-Strong knowledge of analytical instruments like GC-MS, HPLC, and related testing methods.
4-Good understanding of international quality standards and export documentation.
5-Excellent attention to detail, problem-solving, and reporting skills.
Quality Assurance
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Back
Key Responsibilities
Good hands on with writing Test cases/Test Scenarios.
Hands on Testing skills with Functional, Regressions, Sanity tests
Should be good with Integration and E2E testing
Very good testing analogy w.r.t Web UI, Mobile Application, Mobile Web
Should be able to understand the functional aspects
Candidate should be able to upskill the Business E2E knowledge
Exposure to API Testing
Basic Knowledge on DB
Experience with one of the Test Management tools like JIRA
Good understanding of Defect lifecycle
Able to communicate with North American clients
Good with Test Reporting
Required Qualifications To Be Successful In This Role
Very good exposure to Deployment Validation Testing
Review and analyze system specifications and requirements.
Collaborate with QA engineers and developers to develop effective test strategies and test cases.
Conduct post-release/post-implementation testing.
Work with cross-functional teams to ensure quality throughout the software development lifecycle.
Excellent written and oral communication skills since they will be working with the Canada team closely.
Must have attention to details and solutionist mindset
Additional Information
Job Type: Permanent Full Time
Work Profile: Hybrid (Work from Office/ Hybrid)
Years of Experience: 5-8 Years
Location: Bangalore
What We Offer
Competitive salaries and comprehensive health benefits
Flexible work hours and remote work options.
Professional development and training opportunities.
A supportive and inclusive work environment.
Quality Assurance
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About The Role
Create and maintain Quality Assurance Plans for development projects based on ASPICE CL2 compliant QA Process
Execute QA activities based on QA Plans
Report status and progress of QA Plan execution of projects.
Recommend process improvements based on QA metrics and KPIs of projects.
Regularly meet with project stakeholders and ASD QA organization.
Skills:- 1. Creating QA Plans for projects
Finding non-conformances by reviewing work products and auditing processes execution
Identifying project risks
Communicating with project stakeholders
Understanding processes, templates, and methods
Using widely used application tools for documentation, task and issue tracking, configuration management, requirements management, presentation, reporting and communication.
About The Role - Grade Specific
Focus on Electrical, Electronics and Semiconductor. Develops competency in own area of expertise. Shares expertise and provides guidance and support to others. Interprets clients needs. Completes own role independently or with minimum supervision. Identifies problems and relevant issues in straight forward situations and generates solutions. Contributes in teamwork and interacts with customers.
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Quality Assurance
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WE ARE HIRING
Department: QA-IPQA DS Activities
Note: Only for Biological Companies
Only Male candidates
Experience: 3 to 6 years
Qualification: MSC /M Pharmacy/B Pharmacy
Job Responsibilities:
- Line clearance and Monitoring of batches manufactured at multiple stages / Activities in Production DS
- Experience in Downstream process with respect to Handling of AKTA Chromatography Systems, Column Packing and unpacking, TFF system
- Review and monitoring of In-Process quality checks in manufacturing area
Additional Responsibilities:
Involvement in review of Deviations, CAPAs, Risk Assessments, Market Complaints and Product Recalls
Any job assigned by the head of the department and immediate supervisor
Preparation of APQR (Annual Product Quality Review) reports for all the commercial products
Other Duties:
Perform and monitor IPQA activities at shop floor level in each and every stage at.
NOTE : Interested candidates please attach your CV - or whatsapp venkat / Manasa
Quality Assurance
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We're Hiring: QA Intern – Medical Software (Web & Mobile)
Pune | Full-Time | 6-Month Internship | Stipend: ₹15,000/month
Passionate about
tech + healthcare
? Ready to kickstart your QA career with real-world medical software projects? Join
and help build smarter, safer healthcare solutions.
About
We're building the next-gen
AI-powered intelligence stack
for the pharmaceutical industry—equipping global pharma teams with
real-time analytics
,
predictive insights
, and
intelligent agents
. Quality assurance ensures we deliver safe, high-impact products.
Your Role – What You'll Do
- Test web & mobile healthcare applications
- Write & execute manual test cases
- Report bugs via Jira/Trello
- Perform cross-browser/device testing
- Support UAT and validation documentation
What We're Looking For
- Pursuing/completed degree in CS, IT, Biomed, or related
- Understanding of QA, SDLC, STLC
- Manual testing experience (automation is a plus)
- Detail-oriented, analytical, good communication
- Bonus: Jira, Postman, Selenium, JMeter, TestRail
What You'll Gain
Real-world QA experience in regulated medtech
Agile/Scrum environment exposure
6-month paid internship (₹15,000/month)
Internship certificate + full-time offer potential
Apply Now:
Send your resume to
Quality Assurance
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Job Description
Job Title: Head Quality Assurance & Quality Control (QA/QC)
Department: Quality
Location: Tronica City, Ghaziabad (Corporate Office / Manufacturing Unit)
Company: Preet Brothers Ltd. (A Preet Enterprise)
Industry: Heavy Steel Fabrication | EOT Cranes | Material Handling Equipment
Experience: Minimum 10 years in QA/QC leadership, preferably in heavy engineering or fabrication industry
Job Summary
We are hiring a dynamic and experienced Head – Quality Assurance & Quality Control to lead the end-to-end quality operations of our heavy fabrication and crane manufacturing units. The role is responsible for ensuring strict compliance with quality standards from raw material inspection to final product delivery and customer satisfaction.
Key Responsibilities
- Lead the entire Quality function including QA, QC, Vendor Quality, In-Process Inspection, and Final Product Quality.
- Establish and implement Quality Management Systems (QMS) in line with ISO 9001:2015.
- Ensure quality adherence in fabrication, machining, welding, and assembly processes of EOT Cranes and MHE.
- Drive zero-defect culture through process control, defect analysis, and training.
- Define and monitor KPIs (Rejection %, Rework %, Supplier Quality, etc.).
- Conduct internal audits, supplier audits, and ensure closure of Corrective & Preventive Actions (CAPA).
- Ensure compliance with BIS, ISO, statutory norms, and customer specifications.
- Lead customer interactions for FATs (Factory Acceptance Tests), approvals, and resolve quality complaints.
- Promote continuous improvement through RCA, Kaizen, 5S, and Lean practices.
- Drive use of quality tools such as FMEA, SPC, Control Plans, and Six Sigma.
- Develop SOPs and Inspection Checklists for incoming, in-process, and final quality.
- Lead and mentor a high-performing quality team, fostering a culture of excellence and accountability.
Key Skills & Competencies
- Strong understanding of steel fabrication, welding standards (WPS/PQR), machining, and surface treatments.
- Hands-on experience with EOT crane components, heavy fabrication, and large assemblies.
- Proficiency in NDT (UT, RT, MPI, DPT) and dealing with third-party inspections.
- Familiarity with ISO 9001, BIS, ASME, and industry-specific quality norms.
- Effective leadership, communication, and cross-functional collaboration abilities.
Qualifications
- B.Tech / B.E. – Mechanical Engineering (Mandatory)
- Diploma in Mechanical Engineering (Preferred for hands-on experience)
- ISO 9001 Lead Auditor Certification, NDT Level II / III, Six Sigma (Preferred)
Preferred Industry Background
Heavy Engineering | EOT Cranes | Structural Fabrication | Material Handling Systems | Capital Goods Manufacturing
Email for Application
Interested candidates can send their resume to