Engineer II, Software Quality Assurance

Location: Hyderabad, Andhra Pradesh, India

Category: Quality & Regulatory

Employment Type: Full time

Work Schedule

Environmental Conditions

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION:
Join Thermo Fisher Scientific's Quality Assurance team and contribute to our mission to make the world healthier, cleaner and safer. As a Quality Engineer II, you will ensure compliance with quality standards and regulatory requirements across our manufacturing operations. You'll collaborate with cross-functional teams to drive continuous improvement initiatives, lead investigations, and implement corrective actions to maintain our high standards of product quality. This role offers exposure to innovative technologies and the opportunity to directly impact patient care through quality oversight of critical products.

KEY RESPEONSIBILITIES:

• Test Planning & Strategy: Develop detailed and comprehensive test plans, test cases, and test scripts based on functional and non-functional requirements.
• Manual Testing: Conduct functional, regression, and exploratory testing to ensure the application behaves as expected in different scenarios
• Automated Testing (if applicable): Write and maintain automated test scripts using tools like Selenium, TestNG, or others to improve testing efficiency and coverage.
• Bug Identification & Reporting: Identify, document, and track defects in the software. Provide clear and detailed information to developers for reproduction and resolution.
• Collaboration: Work closely with developers, product managers, and other partners to understand project requirements and provide feedback on areas of improvement.
• Test Execution: Complete tests based on test cases and monitor software performance, usability, and stability.
• Performance Testing: Perform load and stress tests to ensure the software can handle expected traffic and usage.
• Documentation: Maintain detailed records of test results, issue reports, and recommendations for improvements.
• Continuous Improvement: Participate in post-release testing and provide insights into test processes for ongoing improvements.

REQUIREMENTS:
• Bachelor's Degree plus 3 years of quality assurance experience in GMP/ISO regulated environments, preferably in medical devices, pharmaceuticals or biotechnology
• Preferred Fields of Study: Life Sciences, Engineering, Chemistry or related scientific/technical field
• ISO 13485/FDA Lead Auditor certification beneficial
• ASQ certification (CQE, CQA) advantageous
• Knowledge of quality systems, cGMP regulations, and standards including ISO 13485, 21 CFR Part 820 & Part 11
• Expertise in quality tools and methodologies including risk management, root cause analysis, CAPA, and change control; including end to end application testing
• Demonstrated experience leading investigations, analyzing quality data, and implementing effective corrective actions
• Excellent documentation and technical writing skills for developing SOPs, protocols and reports
• Strong proficiency in quality management software (ALM, Jira, TrackWise, SAP QM, etc.) and Microsoft Office suite
• Experience supporting internal audits and external regulatory inspections

• Demonstrated ability to build consensus and collaborate across functions
• Strong verbal and written communication skills
• Ability to work independently while contributing effectively in team environments
• Strong attention to detail with analytical and problem-solving capabilities
• Experience with statistical analysis tools and quality metrics reporting
• Project management skills and ability to prioritize effectively
• Ability to work in clean room environments when required
• Foreign language skills beneficial