I
Sr Quality Assurance Engineer (Pharma experience mandatory)
INNOVATOR WEB SOLUTIONSRemote17h ago
RemoteFull-timevia indeed
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Required Skills
gcpsql
Job Description
- *Job Type:** Full Time
- *Job Location:** Remote (WFH)
- *Experience:** 6\-11 years
- *Working Days:** Monday to Friday
- *Working Hours:** 1:00 PM – 10:00 PM IST
- *Key Highlight:** We are looking for experienced Senior QA professionals with strong experience in the Pharma domain.
- *Please Email Your Resume To:** **info@innovatorsol.com**
We are looking for immediate joiners only. Interested candidates can share their updated CV along with their notice period and current/expected compensation. Please note Pharma experience is mandatory which includes FDA 21 CFR Part 11, GLP, GMP and GCP. Kindly provide a brief on these in your email as well.
- *Key Responsibilities**
- Design, develop, and execute test cases for database and data\-driven applications.
- Perform Database Testing, ETL Testing, and Data Validation.
- Write and execute complex SQL queries to validate data accuracy, completeness, and integrity.
- Validate data across source and target systems as part of ETL and data migration testing.
- Identify, document, track, and report defects through the complete defect lifecycle.
- Work closely with development, business, and other QA teams to investigate and resolve issues.
- Ensure testing activities comply with applicable Pharma industry quality and regulatory standards.
- Participate in test planning, execution, defect management, and reporting.
- Contribute to continuous improvement of QA processes and best practices.
- *Required Skills \& Experience**
- 6\+ years of experience in Software Quality Assurance/Testing.
- Mandatory Pharma domain experience.
- Strong hands\-on experience in: Database Testing, ETL Testing, SQL \& Data Validation.
- Good understanding of GxP (Good Practice) requirements within the Pharma/Life Sciences domain.
- Working knowledge of one or more of the following: GLP Good Laboratory Practice, GCP Good Clinical Practice \& GMP Good Manufacturing Practice.
- Understanding of FDA 21 CFR Part 11, particularly requirements related to: Electronic records, Electronic/digital signatures, Data integrity and compliance.
- Strong analytical and problem\-solving skills.
- Excellent verbal and written communication skills.
- Ability to work independently in a remote environment and collaborate effectively with distributed teams.
- *Please Email Your Resume To:** **info@innovatorsol.com**
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Job Overview
- Job type
- Full-time
- Work mode
- Remote
- Location
- Anywhere in India
- Posted
- 17h ago
- Source
- Indeed