Senior Validation Engineer
Responsibilities:
Design, implement, and maintain complex infrastructure systems for high-availability production environments.
Monitor systems and applications for performance, availability, and security, and respond to issues quickly and efficiently.
Continuously improve systems and applications' reliability, scalability, and performance through root cause analysis, code and architecture review, and proactive monitoring.
Participate and respond to critical incidents promptly and efficiently, performing troubleshooting and incident management as needed.
Develop and maintain disaster recovery and business continuity plans to ensure business continuity in case of service outages or disasters.
Provide technical guidance and mentorship to other engineers on reliability and scalability best practices, tools, and methodologies.
Experience in rolling out redundant, mission-critical applications in a highly available production environment.
Familiarity with Databases including Sybase/Mongo/Couchbase.
Familiarity with monitoring Tools including ITRS, Grafana, Prometheus.
Working knowledge on Equity order flow including Client Connectivity, FIX Protocol, Risk Validations will be considered highly advantageous
Knowledge in Cloud and DevOps Tech stack including Jenkins and Git.
Troubleshooting skills on Network.
Previous experience in a Banking/Financial institution
Commissioning, qualification, and validation of biopharmaceutical manufacturing and lab equipment
Perform computer system validation activities including user requirement specifications (URS) and traceability matrices
Conduct risk assessments, gap analysis and risk mitigation activities
Complete validation reports, write summaries of work, and perform statistical analyses
Bachelor’s Degree in Engineering or related scientific field.
Minimum 3 years of experience in a GMP regulated pharmaceutical manufacturing environment.
Extensive knowledge of Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
Experience with commissioning, qualification, and validation (CQV) of pharmaceutical equipment, and computer system validation (CSV)
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