160 Qa Manager jobs in Kochi

   Bachelors/Masters in Science or Diploma /B. Tech In Polymer Technology or any other Subjects.

   Specialization in Biomedical or Quality preferred

   - Strong knowledge of CDSCO(IMDR),ISO 13485:2016, ISO 14971, ISO 11135, GMP

   - Experience in CE MDR compliance, audits, and regulatory submissions

   - Capable of leading QMS, CAPA, and cross-functional quality teams

   Knowledge of regulatory submissions and audits related to GCC countries (e.g., Saudi FDA, UAE MOHAP, SFDA, etc.), US FDA, and other European and African markets.

   Strong understanding of SEDEX platform and ethical audit compliance (SMETA 4-pillar)

   Experience in implementing Lean Manufacturing principles to enhance operational efficiency

   Proficient in tools such as 5S, Kaizen, and Root Cause Analysis to support continuous improvement

   Internal Audits & Management Reviews

   Document & Record Control

   Customer Complaint & CAPA Handling

   Supplier Quality Management

   Risk Management

   Training & Competency

   Cleanroom & Environmental Monitoring

   Post-Market Surveillance (PMS/PMCF/PSUR As per EU MDR)

   QMS Change Control

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.

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.

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.

Job Description

Work location: Kochi. Only preferring Tamil Nadu candidates. Candidate must fluent in Tamil and English

Inmakes Infotech is one of the growing EdTech, officially launched our program for Software Testing (QA) with most advanced Corporate Training, Professional training and On-the job training. We are looking for passionate people with good teaching skills on software testing (Manual Testing), from the software industry, who can teach software Testing to students according to current industry requirement. Job Brief: We are looking for an expert Trainer Member who is confident in Software Testing, who is an experienced and professional software Engineer with a capability of imparting the knowledge of Manual Testing and Selenium-Java to the students.

Job Description :

Should possess strong knowledge of Software Testing, should stay up-todate with the latest testing techniques in the field. Should be able to prepare candidates to work on live projects. Upgrading the students’ knowledge and prepare them to crack the interviews.

Skills Required :

Skills Should have depth knowledge of Manual Testing, Selenium-Java, Sql, ISTQB, Practical knowledge Candidate should have Good Communication Skills Should be able to handle End to End Training – Course Content Preparation, Material Preparation, Interview Questions, Mock Interviews, Live Projects Explanation etc. Should have experience in giving training through online Platform.

Most Expected Requirements :

• Candidate’s must be more passionate to share their skills to new person, who is passionate of learning. • Candidate’s should have a better knowledge in Java scripting and Automation tools based on it such as Cypress, Web driver IO • Candidate(s) should be aware of practical knowledge in Complete QA and QC Process • Candidate’s should have minimum 2+ years of experience in Manual & Automation Testing (Functional / Non-Functional) • Candidate’s must have better real time project experience (Minimum 2+ years) in Selenium with Java / Python • Candidate’s should have project experience in building Automation Frameworks from Scratch • Candidate’s must have better knowledge in API Postman testing & RESTful API Automation Testing • Candidate’s must be aware of BDD Cucumber framework, POM Framework(s)

Key Responsibilities:

• Lead and manage QA efforts across multiple parallel projects

• Define, implement, and manage comprehensive test strategies and test plans

Design, develop, and maintain automation frameworks using Selenium,TestNG, or Cypress

• Conduct end-to-end API testing using tools like Postman, RestAssured, or Swagger

• Perform performance/load testing using tools such as JMeter or equivalent

• Ensure integration of test suites into CI/CD pipelines (Jenkins, GitHub Actions, etc.)

• Own and manage the defect lifecycle using tools like JIRA or Azure DevOps

• Collaborate closely with developers, product managers, and other stakeholders to resolve issues and align expectations

• Mentor and coach junior QA engineers, ensuring adherence to QA best practices and standards

• Maintain clear documentation of test plans, cases, results, and QA metrics.

Required Skills & Qualifications:

8+ years of experience in QA, including at least 2+ years in a lead role

• Strong knowledge of manual testing, functional, UI, and regression testing

• Proficiency in test automation with frameworks like Selenium, TestNG, or Cypress

• Experience in REST API testing using Postman, Swagger, or scripting with RestAssured

• Hands-on experience with JMeter or equivalent performance testing tools

• Familiar with CI/CD tools and version control systems (e.g., Git, Jenkins, GitHub Actions)

Good understanding of SDLC, STLC, and defect life cycle

• Exposure to Agile/Scrum environments

• Excellent communication, reporting, and team collaboration skills.

Preferred/ Optional Skills:

• Knowledge of Docker, Kubernetes, or cloud platforms (AWS, Azure)

• Experience with test case management tools like TestRail or Zephyr

• Exposure to security testing or accessibility compliance

Company Background:

zenda is a financial technology partner to schools, colleges & nurseries, building products exclusively for the education sector. It helps institutions improve collection efficiency, digitize all payments and offers flexibility to parents.

Launched in 2021, zenda is present in 40% of all UAE K-12 schools and ~600 schools across markets, serving 150,000+ parents across UAE, India and Qatar, and on track to process USD 600M+ in transactions this academic year. We are grateful for the positive traction that we have received, including with premium networks such as Nord Anglia, Cognita, Repton, ISP, etc. We are actively launching across KSA, Bahrain, Singapore and other markets over 2024.

zenda is backed by leading VCs including the $1.5bn Saudi Technology Venture, Global Founders Capital, COTU, Venture Souq etc, and is seamlessly integrated with more than 45 local, regional and global SIS/ERP systems.

We are expanding our teams aggressively across functions in the UAE and India, are looking for talent professionals with an entrepreneurial mindset and the passion to create disruptive businesses.

QA Engineer

Location - Bangalore/Kochi

Responsibilities:

• Perform testing of web and mobile applications, ensuring thorough quality checks before go-live sign-offs.
• Analyze functional specifications and design comprehensive test cases.
• Ensure complete test coverage, minimizing any potential defects or leakage.
• Execute regression testing to ensure system stability after updates.
• Develop and maintain automation scripts to enhance testing efficiency.
• Conduct smoke, sanity, and other functional tests as required.
• Identify, reproduce, and track bugs, verifying fixes to ensure resolutions are effective.
• Recommend improvements to optimize user experience and enhance the quality of web and mobile applications.
• Collaborate closely with developers, product managers, and other stakeholders to identify and resolve issues.
• Apply independent judgment and quickly adapt to new tasks and challenges.

Requirements:

• 2-4 years of proven experience in manual testing.
• At least 1 year of experience in automation testing.
• Proficiency in testing web and mobile applications.
• Strong understanding of software QA methodologies, tools, and processes, including experience with JIRA .
• Expertise in writing detailed test scenarios and test cases.
• Experience working in an agile/scrum development environment.
• Excellent communication skills.
• Experience in performance or security testing is a plus.
• Strong analytical and problem-solving abilities.
• A high level of accountability and commitment to quality assurance.