It Manager
Ray Life Sciences Pvt Ltd
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Job summary
Ray Life Sciences Pvt. Ltd. in Bengaluru, Karnataka, seeks an experienced Manager IT to support IT systems for API, Formulations, and Sterile Injectables manufacturing and QC labs.
You will manage IT infrastructure, ensure data backups, data integrity, and deliver technology-driven solutions across manufacturing and quality processes. The role requires understanding GMP, CSV, and regulatory data controls, coordinating with Production, QC, QA, and Engineering teams, and leading the IT support
Qualifications
- Experience in IT operations within the pharmaceutical manufacturing industry.
- Hands-on exposure to manufacturing and QC laboratory environments.
- Understanding of GMP/GxP and data integrity requirements.
- Experience with data backups for QC instruments and data restoration.
Responsibilities
- Understand end-to-end pharmaceutical manufacturing processes across API, Formulations, and Sterile Injectables.
- Collaborate with Production, QC, QA and Engineering to capture requirements and design IT solutions.
- Provide IT solutions to improve efficiency, data management, and reliability.
- Manage IT systems used in manufacturing operations and QC laboratories.
- Ensure IT systems comply with GMP/GxP and data integrity controls.
Skills
Job description
Company: Ray Life Sciences Pvt. Ltd. Ray Group of Companies
Location: Bengaluru, Karnataka
Department: Information Technology
Reporting To: Director
We are looking for an experienced IT professional with strong exposure to the pharmaceutical manufacturing industry, particularly API, Formulations, and Sterile Injectables.
The candidate will be responsible for managing IT systems supporting manufacturing and Quality Control (QC) operations, ensuring regular data backups for QC instruments, maintaining data integrity, and providing technology-driven solutions to manufacturing and quality-related processes.
The ideal candidate should understand pharmaceutical manufacturing workflows, QC laboratory operations, and applicable GMP and data integrity requirements, and be capable of translating operational requirements into effective IT solutions.
- Understand end-to-end pharmaceutical manufacturing processes across API, Formulations, and Sterile Injectables.
- Work closely with Production, Quality Control (QC), Quality Assurance (QA), and Engineering teams to understand operational and technical requirements.
- Identify process-related challenges and provide appropriate IT solutions to improve efficiency, reliability, and data management.
- Support IT systems used in manufacturing operations and QC laboratories.
- Take ownership of scheduled weekly and monthly data backups for QC instruments and associated systems.
- Ensure the availability, integrity, security, and retrievability of QC instrument data.
- Establish and maintain documented backup schedules, backup records, and periodic verification of backup completeness and restoration.
- Coordinate with QC teams and instrument vendors to resolve data storage, retrieval, connectivity, and system-related issues.
- Ensure appropriate access controls and secure storage of electronic records.
- Manage IT infrastructure supporting pharmaceutical manufacturing facilities, including servers, networks, storage, and backup systems.
- Support applications, databases, laboratory systems, and manufacturing-related software.
- Ensure system availability, troubleshooting, preventive maintenance, upgrades, and disaster recovery.
- Coordinate with vendors for system integration, application support, and technical issue resolution.
- Ensure IT systems supporting regulated operations comply with applicable GMP, GxP, and data integrity requirements.
- Support audit readiness, Computer System Validation (CSV), SOPs, change control, and IT documentation, as applicable.
- Maintain appropriate controls for electronic records, user access, data backup, and recovery.
- Support compliance with applicable electronic records requirements, including FDA 21 CFR Part 11, wherever relevant.
- Analyse operational challenges in manufacturing and QC processes and recommend practical technology solutions.
- Provide technical support for instrument connectivity, data transfer, application performance, and system integration.
- Work with cross-functional teams to minimise system downtime and ensure business continuity.
- Identify opportunities to improve process efficiency through digitalisation and automation.
- Implement and monitor cybersecurity controls, user access management, antivirus, firewalls, and data protection measures.
- Manage IT assets, software licences, vendors, service agreements, and support activities.
- Lead the IT support team, monitor issue resolution, and ensure timely technical assistance.
- Support IT budgeting, infrastructure planning, and implementation of technology projects.
- Pharmaceutical Manufacturing IT
- API / Formulations / Sterile Injectables
- QC Laboratory Instrument Data Management
- Weekly and Monthly Data Backup & Restoration
- GMP / GxP / Data Integrity
- Computer System Validation (CSV)
- Laboratory Information Systems and Instrument Software
- Server, Network, Storage & Backup Management
- Electronic Records and Access Control
- IT Troubleshooting and Process Improvement
- Vendor Management and Cross-functional Coordination
- Relevant experience in IT operations within the pharmaceutical manufacturing industry.
- Hands-on exposure to manufacturing and QC laboratory environments.
- Understanding of pharmaceutical manufacturing workflows and Quality Control processes.
- Experience managing data backups for QC instruments and maintaining data integrity.
- Ability to understand operational problems and implement suitable IT solutions.
- Strong troubleshooting, documentation, coordination, and problem-solving skills.
Candidates with experience in API, Formulations, or Sterile Injectable manufacturing facilities and exposure to GMP-regulated QC laboratories.
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