Validation Engineer

About Company : · Our is Client is a largest Top 5 Software giant in India, with over 11.3 USD billion dollars revenue, Global work force 2,40,000 employees, It delivers end-to-end technology, consulting, and business process services to clients across the globe, Presence: 60+ countries and Publicly traded company NSE & BSE (India), NYSE (USA).

.Job Title: Validation Engineer

· Location: Hyderabad

· Experience: 6+ yrs

· Job Type : Full - Time

· Notice Period:- Immediate joiners.

Mandatory Skills:

JD :Validation Engineer

Primary Function of Position

This position's primary role is to work closely with the internal IT teams and cross functional departments (Business & PQ-CSV) to support computer system validation activities related to projects and change requests.

Essential Job Duties

• Responsible for oversight of all GxP-regulated computerized systems at all applicable points of the computerized system lifecycle, ensuring compliance with regulatory requirements, Computer Systems Validation (CSV), and Lifecycle procedures with Data Integrity requirements.
• Provide oversight of validation activities, lead the development and approval of validation documentation and risk assessments, work with project teams to determine which elements should be validated, and conduct impact assessment of proposed changes to computerized systems.
• Perform and/or direct GxP computerized system validation projects in compliance with 21 CFR 820, 21 CFR Part 11, Annex 11, and Data Integrity.
• Ensure that GxP systems meet intended uses and comply with applicable regulations, current industry practices, and Intuitive Surgical policies and procedures.
• Development and approval of Validation Plans, IQ, OQ Protocols, Trace Matrices, Risk Assessments and Validation Summary Reports.
• Establish validation standards, develop testing protocols, document test results and maintain records for later analysis.
• Documentation and remediation of deviations resulting from validations/qualifications.
• Provide assistance and guidance in training co-workers on validation protocols and operating procedures.
• Author/Update assigned Operating Procedures (SOPs & DOPs), Policies, validation templates to ensure compliance with Company policies and federal regulations.
• Support regulatory agency inspections/audits, as required.
• Must be familiar with cGMPs and current industry guidelines.
• Interfaces between various internal and external functional areas to assure successful integration and completion of validation activities in overall project schedules.
• Maintains awareness of regulatory requirements.
• Understanding of FDA’s new guidance of CSA risk based approach validation.

Required Skills and Experience

• Bachelor’s degree (B.S.) in related field or equivalent.
• 5-8 years hands-on experience in Computer System Validation/Quality Compliance in a FDA Regulated industry (Medical Device/Pharma/Life Sciences) with a focus on GxP system.
• Knowledge of fundamental cGMP concepts and FDA/EMA regulations, QSR, 21 CFR Part 820, 21 CFR Part 11, and ISO 9001 Standards.
• Strong knowledge of FDA Regulated manufacturing processes, process validation, computer and equipment validation, and GMPs.
• Hands-on experience in EDMS (Electronic Document Management system) & Test Management tools.
• Understanding of FDA’s recent guidance on transition of CSV to CSA.
• Ability to develop clear, concise, and timely oral and written reports. Excellent written and oral communication skills.
• Ability to work on complex projects with general direction and minimal guidance.
• Ability to handle multiple projects and meet deadlines.
• Ability to manage priorities and workflow. Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm.