135 Quality Control Specialists jobs in Anand

Job Description

Role: QA Specialist

Location: Hyderabad

Full/ Part-time: Fulltime

Build a career with confidence.

Kidde Global solutions (“KGS”) is a Global Technology Leader in Fire and Life Safety Solutions. It is world Leader in Fire and Life Safety, constantly building upon new products and services that improve global Fire and Life safety and efficiency, with more than two centuries of combined history, our brands including

Kidde, Kidde Commercial, Edwards, GST, Badger, Gloria and Aritech have been leading the way in protecting people and property around the world. From the beginning, we've led in inventing new technologies and entirely new industries. Today, we continue to lead because we have a world-class, diverse workforce that puts the customer at the center of everything we do.

About the role

The candidate will be part of KGS Hyderabad Design team working with dynamic cross functional global QA team performing Systems requirements analysis, Designing and implementing tests for our next generation products. Testing Smart Home Solutions involves Hardware, Firmware, Cloud & Mobile applications. Individual must have the ability to analyze the system requirements and develop and execute exploratory and automated tests to ensure product quality The selected candidate must have a background in testing Firmware, Cloud iOT, Mobile application and devices/system interaction and troubleshooting and will be involved in all aspects of the QA process (Analysis, Estimate, Plan, Execute and Release). The selected candidate will interact frequently with technical program management both locally and global team. Will need to work with customers at global locations across different time-zone.

Key Responsibilities:

As a QA Specialist , you’ll be responsible for:

• Lead and Mentor the Test and Validation team with advanced Software Testing Skills with good domain knowledge in Residential Fire Safety and Security products.
• Work on Embedded IoT products and collaborate with peer/lead engineer to troubleshoot/resolve/reported issues across different design centers and manufacturing teams.
• Work with product management and system engineering teams to understand the product requirements and drive the test development and executions.
• Develop Test Plan and monitor/manage Test Execution
• Learn and apply project high-level and detailed business requirements.
• Development experience automation scripts for Embedded Firmware, Mobile and Cloud Applications
• Analyze requirement and design Test strategy, test estimation.

Requirement

• Requires advanced to expert knowledge obtained through advanced education, combined with experience with Excellent written and communication skills.
• University Degree or equivalent and a minimum of 13+ years prior relevant experience in testing embedded connected products.
• Hands on experience in validating RS-232/485, Network (TCP/IP, UDP etc.), wireless technologies like Wi-Fi, Sub-GH, Bluetooth protocols
• Hands on development knowledge of C, C#, Java, API Testing & PyTest Frameworks or any programming language
• Must have end of end test methods for Embedded IoT products and System level testing and know how about product life cycle testing methods.
• Expertise Automation tools such Jenkins, CI/CD tools,
• Good understanding and hands on experience of Python and Automation Frameworks E.g.: TDD, BDD.
• Working knowledge of Git, JIRA

About Kidde Global Solutions (KGS)

Kidde Global Solutions (KGS) is a leading manufacturer of residential and commercial fire and life safety products. With a strong legacy of innovation, we provide advanced solutions to protect people and property from fire and related hazards worldwide. Our products are found in homes and businesses globally, bringing together the most trusted brands in safety and security. By leveraging our expertise and experience, we deliver cutting-edge solutions that ensure safety across various applications worldwide.

QA-Compliance – Sterile Injectables

Experience Required: 10-15 years

Location: Remote

Department: Quality Assurance

No. of vacancy: 01

Key Responsibility:

• Prepare and review QMS-related documents, including SOPs, work instructions, and templates for validation, qualification, and compliance processes.
• Review, approve, and trend Change Control (CC) records, assessing potential impact on validation, process performance, and regulatory compliance.
• Handle deviations by reviewing deviation reports, assessing adequacy of root cause analysis, recommending corrective/preventive actions, and ensuring timely closure in compliance with procedural requirements.
• Review, approve, and trend deviations for recurrence patterns and systemic issues; prepare periodic deviation trend analysis reports for management.
• Review and approve market complaint investigations, ensuring thorough root cause identification, adequacy of corrective/preventive actions, and compliance with regulatory timelines.
• Review and approve investigation reports for OOS (Out-of-Specification), OOT (Out-of-Trend), and any critical quality incidents, ensuring accuracy, completeness, and regulatory compliance.
• Conduct remote compliance checks of controlled documents to ensure adherence to cGMP, US FDA, and other applicable regulatory requirements.
• Manage vendor quality activities remotely, including review of vendor qualification/approval documentation, participation in vendor audits (virtual or on-site as required), and review of vendor audit reports.
• Handle vendor quality notifications and change notifications by reviewing the impact on processes, products, and regulatory compliance, and coordinating required actions with relevant departments.
• Support and participate in virtual internal and external audits, providing requested documentation, clarifications, and evidence.
• Monitor and trend QMS performance metrics (e.g., CC closure rates, deviation frequency, CAPA on-time completion, vendor performance metrics) and prepare quarterly quality performance reports for management.

Key Skills and Competencies:

• In-depth knowledge of sterile injectable manufacturing processes and aseptic techniques.
• Expertise in validation methodologies and regulatory guidelines (US FDA, cGMP etc.).
• Strong analytical and problem-solving skills.
• Effective communication and documentation skills.
• Ability to manage cross-functional teams and prioritize tasks.
• Proficiency in QMS tools and software.

Education and Qualifications:

• Bachelor’s/Master’s degree in Pharmacy, Biotechnology, Microbiology, or related field.

QA-Compliance – Sterile Injectables

Experience Required: 10-15 years

Location: Remote

Department: Quality Assurance

No. of vacancy: 01

Key Responsibility:

• Prepare and review QMS-related documents, including SOPs, work instructions, and templates for validation, qualification, and compliance processes.
• Review, approve, and trend Change Control (CC) records, assessing potential impact on validation, process performance, and regulatory compliance.
• Handle deviations by reviewing deviation reports, assessing adequacy of root cause analysis, recommending corrective/preventive actions, and ensuring timely closure in compliance with procedural requirements.
• Review, approve, and trend deviations for recurrence patterns and systemic issues; prepare periodic deviation trend analysis reports for management.
• Review and approve market complaint investigations, ensuring thorough root cause identification, adequacy of corrective/preventive actions, and compliance with regulatory timelines.
• Review and approve investigation reports for OOS (Out-of-Specification), OOT (Out-of-Trend), and any critical quality incidents, ensuring accuracy, completeness, and regulatory compliance.
• Conduct remote compliance checks of controlled documents to ensure adherence to cGMP, US FDA, and other applicable regulatory requirements.
• Manage vendor quality activities remotely, including review of vendor qualification/approval documentation, participation in vendor audits (virtual or on-site as required), and review of vendor audit reports.
• Handle vendor quality notifications and change notifications by reviewing the impact on processes, products, and regulatory compliance, and coordinating required actions with relevant departments.
• Support and participate in virtual internal and external audits, providing requested documentation, clarifications, and evidence.
• Monitor and trend QMS performance metrics (e.g., CC closure rates, deviation frequency, CAPA on-time completion, vendor performance metrics) and prepare quarterly quality performance reports for management.

Key Skills and Competencies:

• In-depth knowledge of sterile injectable manufacturing processes and aseptic techniques.
• Expertise in validation methodologies and regulatory guidelines (US FDA, cGMP etc.).
• Strong analytical and problem-solving skills.
• Effective communication and documentation skills.
• Ability to manage cross-functional teams and prioritize tasks.
• Proficiency in QMS tools and software.

Education and Qualifications:

• Bachelor’s/Master’s degree in Pharmacy, Biotechnology, Microbiology, or related field.