325 Quality Assurance jobs in Ahmedabad

Company:
Zydus Medtech Pvt Ltd

Reporting:
Zydus Medtech Head

Location:
Ahmedabad

Key Responsibilities

The Lead of Quality Assurance and Regulatory Affairs will be a senior leadership role reporting directly to the BU Head. This position is responsible for the strategic direction, oversight, and execution of all Quality Assurance (QA) and Regulatory Affairs (RA) functions across 3 BUs of Zydus Medtech, ensuring compliance with national and international standards, and supporting innovation and market expansion.

Strategic Leadership & Governance

• Develop and implement QA and RA strategies aligned with business goals
• Lead cross-functional teams to ensure quality and regulatory compliance throughout the product lifecycle
• Represent the company in regulatory and quality discussions with external stakeholders, including regulatory bodies, partners, and auditors
• Provide regular updates and reports to the Leadership and Board on compliance status, risks, and strategic initiatives

Quality Assurance

• Oversee the Quality Management System (QMS) ensuring compliance with ISO 13485, GMP, GDP, GVP, and MDD/MDR standards
• Lead internal and external audits, inspections, and quality improvement initiatives
• Manage CAPA (Corrective and Preventive Actions), non-conformance, and complaint handling processes
• Ensure validation of equipment, processes, and software used in manufacturing and testing
• Supervise final batch release, documentation control, and production line clearance
• Champion continuous improvement initiatives and foster a culture of quality across the organization

Regulatory Affairs

• Develop and execute regulatory strategies for India and international markets (US FDA, EU MDR, etc.)
• Ensure timely regulatory submissions, product registrations, and lifecycle management
• Maintain compliance with MAH requirements and marketing practices
• Lead regulatory due diligence for licensing, acquisitions, and partnerships
• Monitor and communicate changes in regulatory requirements to senior management
• Coordinate Medical Device Reporting (MDR), product recalls, and safety notifications
• Act as primary contact for correspondences, inquiries, inspections with external agencies (e.g. regulatory authorities)

Personnel & Team Management

• Lead and mentor QA and RA teams, defining roles, responsibilities, and KPIs
• Conduct performance appraisals, training plans, and succession planning
• Promote a positive working environment and team collaboration
• Manage departmental budgets and resource allocation efficiently

Operational Excellence

• Oversee supplier qualification, audits, and performance monitoring
• Ensure compliance with customer-specific quality requirements and contract reviews
• Manage change control systems and ensure proper documentation and traceability
• Support R&D and product development teams from concept to launch
• Drive implementation of electronic QMS and digital transformation initiatives
• Manage post market / post launch regulatory and quality activities

Qualifications & Experience:

• Master's degree in Pharmacy, Chemistry, Biotechnology, Biomedical Engineering, or related field
• Minimum 15 years of experience in QA and RA, with at least 5 years in a leadership role in the medical device or pharmaceutical industry
• Proven expertise in ISO 13485, FDA 21 CFR Part 820, EU MDR, GMP, GDP, and GVP
• Experience in hosting and leading audits by regulatory authorities (FDA, CDSCO, EU Notified Bodies)
• Strong project management, analytical, and problem-solving skills
• Excellent communication, interpersonal, and leadership abilities
• Proficiency in Microsoft Office and QMS software tools
• Regulatory Affairs Certification (RAC) or equivalent preferred

Preferred Skills:

• Experience in regulatory submissions for clinical studies
• Certified Internal/External Auditor
• Exposure to Pharmacovigilance (GVP)
• Implementation of electronic QMS platforms
• Strategic planning and risk mitigation capabilities

Roles and Responsibilities

• Ensure compliance with cGMP guidelines during line clearance activities.
• Conduct BMR reviews, BPR reviews, and stability analysis reports.
• Review SOPs, protocols, and reports related to quality assurance.
• Perform material release and batch release tasks.
• Verify documents such as BMR, BPR, Stability Analysis Report, etc.

Job location: Ahmedabad

Experience Required- 1+ years of experience in QA (Clinical Research)

Role & responsibilities

A. Review Protocol and its attachments.

B. Conduct in-process and retrospective audit of clinical phase of the study to ensure compliance to protocol, SOPs and applicable regulatory requirements.

C. Review Clinical report to verify that the data reported in the report, accurately reflects the raw data and to ensure that the report is prepared in compliance with SOP, ICH E3 and applicable regulatory requirements.

D. Conduct system audits as per the system audit plan.

E. Conduct vendor pre-qualification and re-qualification audits as per the vendor audit plan.

F. Preparation, Review, distribution, maintenance, recall and destruction of QMS Documents (SOPs, Policies, WIs, Manuals, forms and Plans . )

G. Review and maintain calibration, validation and Mapping documents and Temperature data / OOS data (Eurotherm data )review.

H. Issuance of logbooks.

I. Review of deviations, event and change control procedures and provide number to respective document.

J. Provide Instrument IDs as per SOP.

K. To maintain/update study/System specific tracker/Index on on-going basis.

L. Assisting Team in charge in Regulatory/Sponsor Audit.

M. Maintain Master Signature Log.

Job Summary

We are seeking a skilled and detail-oriented QA Automation Engineer with 4 to 5 years of experience

to join our quality assurance team. The ideal candidate will have strong experience in test

automation, API testing, and working within modern DevOps environments. You'll collaborate with

cross-functional teams to ensure the delivery of high-quality, scalable, and reliable applications.

Key Responsibilities

• Design, develop, and maintain automated test scripts using Selenium, Cypress, or

Playwright.

• Debug test failures and provide clear, actionable feedback to developers to support rapid

issue resolution.

• Perform comprehensive API testing using tools like Postman and automation frameworks.
• Integrate automated tests within CI/CD pipelines (e.g., Jenkins) to support continuous

testing and delivery.

• Collaborate closely with developers, QA engineers, and product managers to define quality

benchmarks and improve testing practices.

• Apply the Page Object Model (POM) design pattern to enhance test maintainability and

scalability.

• Work with databases and create SQL queries for validation of test scenarios and backend

testing.

• Follow best practices in SDLC and STLC, ensuring quality at every stage of the software development

lifecycle.

• Stay current with the latest tools, trends, and practices in software testing and automation.

Required Qualifications

• Bachelors degree in Computer Science, Engineering, or a related technical field.
• 56 years of experience in software testing, with a strong focus on automation.
• Proficiency with automation tools such as Selenium, Cypress, or Playwright.
• Hands-on experience with API automation, Postman and Rest assure, and Cypress.
• Solid experience with CI/CD tools like Jenkins.
• Proficient in using Git for version control.
• Working knowledge of SQL and databases for test validation.
• Strong analytical and debugging skills with a keen eye for detail.
• Excellent verbal and written communication skills.
• Software Testing Life Cycle (STLC) methodologies.

Nice to Have: Salesforce Testing, hands-on knowledge of ACCELQ Testing

Our Shift timings are 2:00 pm to 11:00 pm - Work From Office - Monday to Friday. We have a Deployment on every alternate Saturday, but for that, we give weekdays off.

As a QA/QC Engineer at HN Safal, you will be responsible for ensuring quality assurance and quality control across all stages of project execution. The role involves preparing and managing quality documentation, conducting audits, monitoring compliance, and coordinating with site teams, vendors, and clients to maintain the highest construction and safety standards.

Job Description

About the Role

• Prepare, update, and supervise the company’s QA/QC manual including all amendments and revisions.
• Control and distribute all company quality documentation.
• Monitor all quality-related activities across assigned projects.
• Perform internal and external audits on behalf of company management.
• Verify contractor quality requirements and review vendor/contractor documentation submittals.
• Attend pre-bid meetings and coordinate project quality requirements with bidders.
• Attend client quality management meetings and represent the company in QA/QC matters.
• Prepare and control project quality system documentation prior to project commencement.
• Review and assess qualifications and training needs of quality inspection personnel.
• Monitor and close out nonconformance reports, ensuring corrective actions are taken.
• Track and improve the effectiveness of the project’s Quality Management System (QMS).
• Coordinate QA/QC activities with site managers, procurement managers, and customer representatives.
• Ensure proper statistical reporting methods are applied where required.
• Address, action, and close all customer complaints related to quality.
• Control and archive all quality documentation upon project completion.

About You

• Minimum Qualification: B.E. / Diploma in Civil Engineering (specialization in Quality Management preferred).
• Minimum Experience: 5–8 years in QA/QC roles within the real estate or construction industry.
• Software Knowledge: Proficiency in MS Office, AutoCAD, and ERP systems.
• Skills: Strong knowledge of ISO standards, quality systems, and construction QA/QC practices.
• Communication: Excellent verbal and written communication in English, Hindi, and Gujarati.

Why Join HN Safal?

At HN Safal, one of Ahmedabad’s leading real estate developers, you will be part of a company shaping the way people live, work, and grow. We offer:

• The opportunity to work on landmark projects with high-quality standards
• Strong focus on career growth and continuous learning
• A collaborative workplace that values diversity, inclusion, and teamwork
• Work-life balance in a supportive and rewarding environment

We provide autonomy, structured systems, and technology-driven tools to help our people excel while rewarding contributions with a comprehensive benefits program.

Company Description

Weatherford International plc (Nasdaq: WFRD) is a leading global energy services company operating in approximately 75 countries. With a talent network of about 17,000 team members and around 350 operating locations, the company excels in addressing challenges in the energy sector. Weatherford's facilities include manufacturing, research and development, service, and training locations.

Role Description

This is a full-time on-site role for a Quality Assurance Quality Control Inspector based in Ahmedabad. The QA/QC Inspector will be responsible for ensuring the quality and compliance of products through various inspections and quality management processes. Daily tasks include performing inspections, quality assurance, and quality control activities, as well as overseeing welding inspections as needed.

Qualifications

• Skills in Quality Control, Quality Assurance, and Quality Management
• Experience with Inspection processes and procedures
• Proficiency in Welding Inspection
• Strong attention to detail and analytical skills
• Excellent problem-solving abilities
• Ability to work collaboratively with cross-functional teams
• Bachelor's degree in Engineering or a related field is preferred
• Relevant certifications in quality inspection and quality assurance are a plus

Company Description

Azista Industries Private Limited and Berlin Space Technologies GmBH have partnered to establish a unique small satellite production facility in Ahmedabad. This is India's first private-scale satellite production house and one of the first satellite production lines in the world. The initiative aims to revolutionize satellite production, compared by one of the BST founders to the "Henry Ford moment" for satellites.

Job Summary

We are seeking a highly motivated QA/QC Engineer to ensure the reliability, safety, and compliance of space-grade components and systems. The role involves overseeing quality processes across design, manufacturing, assembly, integration, and testing phases of spacecraft & subsystems such as avionics, power & Control systems, and payloads.

Role: QA/QC Engineer.

No. Of Positions Electronics QA: 02.

No. Of Positions Electronics QC: 01.

Key Responsibilities

 Quality Assurance (QA)

• Develop and implement quality plans, procedures, and standards (e.g., ISRO-PAS, ECSS, MIL-STD).
• Participate in design reviews (SRR, PDR, CDR) to ensure quality requirements are embedded.
• Conduct audits and process evaluations across vendors and internal teams.
• Ensure traceability and configuration control of components and documentation & Version control of Designs as well as documents.
• Support risk management and failure mode analysis (FMEA, FTA).

 Quality Control (QC)

• Perform inspection and testing of incoming components, in-process assemblies, and final products.
• Monitor and verify compliance with ATPs (Acceptance Test Procedures), PID, and DTRs.
• Coordinate environmental testing (thermal, vibration, EMI/EMC) and review results.
• Investigate non-conformances and lead root cause analysis and corrective actions.
• Maintain calibration and certification records of test equipment.

Required Qualifications

• Bachelor's or Master's degree in Electrical or Electronics Engineering.
• 2-3 years of experience in QA/QC roles, preferably in aerospace or space systems.
• Familiarity with standards like ECSS, ISRO-PAS, MIL-STD-883, IPC-A-610.
• Hands-on experience with inspection tools, test benches, and environmental chambers.
• Strong documentation, analytical, and communication skills.

Preferred Skills

• Experience with satellite subsystems (e.g., Reaction Wheel, Battery, EPS, CDH).
• Experience with satellite Assembly & Integration QA/QC.
• Knowledge of reliability engineering and statistical quality control.
• Exposure to cleanroom protocols and ESD-safe handling.
• Certification/Knowledge in Six Sigma, AS9100, or ISO 9001 is an additional value.