Total 6 job vacancies by Itcan Pte. Limited

Key Responsibilities

• Develop and maintain automated test scripts/frameworks
• Execute functional, regression, integration, API, and UI testing
• Identify, document, and track defects using bug-tracking tools
• Analyze test results and prepare reports
• Collaborate with developers to resolve issues
• Participate in requirement analysis and test planning
• Improve CI/CD testing processes
• Ensure software meets quality standards before release

Required Skills

Technical Skills

• Automation tools: Selenium, Cypress, Playwright, Appium, UFT, etc.
• Programming languages: Java, Python, JavaScript, C#, etc.
• API testing: Postman, Rest Assured
• Test frameworks: TestNG, JUnit, PyTest
• CI/CD tools: Jenkins, GitHub Actions, GitLab CI
• Version control: Git

Key Responsibilities

• Define and implement comprehensive QA strategies, standards, and governance frameworks for ICT systems.
• Lead end-to-end testing efforts including functional, integration, system, regression, API, and performance testing.
• Design and develop automation frameworks using tools such as Selenium, Playwright, and Robot Framework.
• Integrate automated testing into CI/CD pipelines using tools like Jenkins, GitLab, Maven, and Docker.
• Collaborate with cross-functional teams including developers, product owners, and stakeholders to ensure quality delivery.
• Manage defect lifecycle, perform root cause analysis, and drive continuous improvement initiatives.
• Ensure compliance with security, regulatory, and government standards for ICT systems.
• Establish and monitor quality metrics, KPIs, and reporting dashboards.
• Lead and mentor QA teams, promoting best practices in Agile and Scrum environments.
• Support UAT, SIT, and production releases, ensuring system stability and reliability.

Technical Skills & Tools

• Automation & Testing Tools: Selenium, Playwright, Robot Framework, Cucumber, TestNG, Appium
• API & Performance Testing: Rest Assured, JMeter
• Programming Languages: Java, Python, TypeScript
• DevOps & CI/CD: Jenkins, GitLab, Maven, Docker
• Test Management & Collaboration: JIRA, TestLink, Confluence, Bitbucket

Qualifications

• Bachelor’s or Master’s degree in Computer Science, Information Technology, or related field (MCA preferred).
• 10+ years of experience in software quality assurance, with at least 5 years in a leadership or specialist role.
• Strong experience in ICT systems, enterprise applications, or government platforms.
• Proven ability to design scalable automation frameworks and drive test automation adoption.
• Experience working in Agile/Scrum environments with distributed teams.

Skills

• Selenium, Playwright, Robot Framework, Cucumber, TestNG, Appium, Testing, Quality Assurance

1.     Hands on experience inpreparing & executing test cases, test scenarios for both automation andmanual testing

2.     Skills on Automationframework design pattern and techniques, hands on experience on developing BDDautomation framework, Cucumber, TestNG

3.     Strong in Java (conceptsand programming skills)

4.     Good experience on webservice / API test automation and UI automation

5.     Strong DB and API testingskills

6.     Good Automation skillsusing, Java & Selenium

7.     Hands on knowledge on CI/CDtools (i.e. Jenkins / Gitlab)

8.     Very good knowledge of Gitlab/Bitbucket/GitHuband branching strategies and Git commands

9.     Experience on OFS testautomation will be preferable

10.  Decent knowledge of Maven

11.   Good Knowledge & experience on SQL DB(concepts and queries)

12.  Experience in working on anAgile Environment

13.  Strong analytical andorganizational skills with a demonstrated aptitude to understand technicalenvironments.

14.  Strong desire to learn newtechnical skills and grow with latest technical trends.

15.  Experience working withTools like Swagger, JIRA, Confluence, Gitlab, Soap UI and Postman

16.  Ability to multi-task in afast-paced environment & prioritize workload and maintain focus.Self-motivated and able to work under pressure.

17.  T24, TAP, TPH & BFSdomains is a plus and value add

We are looking for a skilled with Empower expertise to join our team on a long-term project supporting diverse Life Sciences initiatives.

Key Attributes/Responsibilities:

• Serve as the Subject Matter Expert (SME) for Waters Empower Chromatography Data System (CDS) within GMP laboratory environments.
• Lead or support computerized system validation (CSV) activities for Empower, including URS, risk assessment, IQ/OQ/PQ, and validation documentation.
• Configure, administer, and maintain Empower projects, user roles, audit trails, and data integrity controls in compliance with GxP and ALCOA+ principles.
• Provide technical support and troubleshooting for chromatography systems integrated with Empower.
• Support qualification and lifecycle management of analytical instruments connected to Empower.
• Experience with Waters HPLC/UPLC systems is required; experience with Thermo Scientific LCs, Agilent GC-HS, Sciex CE, or ProteinSimple iCIEF is an advantage.
• Collaborate with QA, QC laboratories, and IT to ensure regulatory compliance with FDA 21 CFR Part 11 and EU Annex 11.
• Support audits, data integrity reviews, and periodic system assessments.
• Prepare and review validation documentation and provide SME guidance during regulatory inspections.

Requirements / Qualifications

• Bachelor’s degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Biotechnology, or a related scientific discipline.
• Minimum 3–5+ years of hands-on experience with Waters Empower Chromatography Data System (CDS) in a GMP-regulated environment.
• Strong knowledge of computerized system validation (CSV) processes, including URS, risk assessments, IQ/OQ/PQ, and lifecycle documentation.
• Proven experience in Empower system administration, including project setup, user management, audit trails, and data integrity controls.
• Solid understanding of GxP regulations, ALCOA+ principles, and data integrity requirements.
• Experience supporting and troubleshooting chromatography systems (HPLC/UPLC) integrated with Empower.
• Familiarity with instrument qualification and lifecycle management for analytical laboratory systems.
• Working knowledge of regulatory requirements such as FDA 21 CFR Part 11 and EU Annex 11.
• Experience supporting audits, inspections, and data integrity reviews.
• Strong documentation skills with the ability to prepare, review, and manage validation documents.

Role Summary
We are seeking an experienced QC Systems Specialist with strong expertise in laboratory equipment computer system validation (CSV) and hands-on exposure as a laboratory equipment within GMP-regulated environments. The role will support the full lifecycle of QC laboratory systems and equipment, providing validation oversight, qualification guidance, change control support, and data integrity assurance while working closely with Quality, Validation, Engineering, and Operations teams.

Key Responsibilities

• QC Qualification Engineer (lab Analytical Computerized System).
• Support Change Controls initiation and end-to-end ownership for lab Analytical Computerized System Qualification.
• Responsible for Drafting and executing Validation related documents (Validation Plan & Requirement, IOQ/PQ Test Scripts, Summary report, Data Integrity Risk Assessments).
• Responsible for Drafting system decommissioning related documents (Decommissioning plan, summary report).
• Responsible for Drafting Operations and Maintenance SOPs.
• Support in generation of Preventive Maintenance program for System.  
• Coordination with equipment vendor for vendor qualification activities.
• Coordination with different stakeholders’ functions (F&E, QA, QC, IT).

Requirements

• Related working experience in biotech or pharmaceutical operation environment is preferred.
• Strong understanding of various validation approaches, strategies and philosophies.
• Working knowledge of lab instruments and computerized system validation, controlled temperature chambers qualification etc.
• Working experience with KNEAT / electronic validation tools are preferred.
• Experience with change control methodology
• Good knowledge in data integrity, GMP and GDP
• Ability to facilitate and work in a collaborative team-based environment.
• Team player with strong focus on safety, quality and timeline
• Able to work independently with minimal supervision

Responsibilities

• Support Change Controls initiation and end-to-end ownership for Temperature Chambers (Fridges/ Freezers/ Incubators).
• Responsible for Drafting and executing Validation related documents (Validation Plan & Requirement, IOQ/PQ Test Scripts, Summary report, Data Integrity Risk Assessments).
• Responsible for Drafting Operations and Maintenance SOPs.
• Support in generation of Preventive Maintenance program for Temperature Chambers.   
• Coordination with equipment vendor for vendor qualification activities Coordination with different stakeholders’ functions (F&E, QA, QC, Automation, IT).     
• Coordination for Calibration of Temperature Chambers (Fridges/ Freezers/ Incubators).

 Requirements

• Related working experience in biotech or pharmaceutical operation environment is preferred.       
• Strong understanding of various validation approaches, strategies and philosophies.       
• Working knowledge of lab instruments and computerized system validation, controlled temperature chambers qualification etc.        
• Working experience with KNEAT / electronic validation tools are preferred.        
• Experience with change control methodology.       
• Good knowledge in data integrity, GMP and GDP.       
• Ability to facilitate and work in a
• collaborative team-based environment.       
• Team player with strong focus on safety, quality and timeline.       
• Able to work independently with minimal supervision.