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4.0 - 8.0 years
10 - 20 Lacs
Ahmedabad
Work from Office
Responsible for Production planning ,finite scheduling with plant team to ensure the efficient delivery of inventory, service and cost objectives. Manage FG inventory, highlight risks of CFR cuts, come up with RCAs and ensure CFR of 98%+ Required Candidate profile Good exposure into continuous improvement initiatives improve processes, cost reduction ideas, supply chain cost optimization opportunities, or business process initiatives.
Posted 4 months ago
6.0 - 11.0 years
7 - 12 Lacs
Hyderabad
Work from Office
At Capgemini Invent, we believe difference drives change. As inventive transformation consultants, we blend our strategic, creative and scientific capabilities,collaborating closely with clients to deliver cutting-edge solutions. Join us to drive transformation tailored to our client's challenges of today and tomorrow.Informed and validated by science and data. Superpowered by creativity and design. All underpinned by technology created with purpose. The GxP CSV Validation Engineer ensures that digital systems used in clinical development comply with regulatory standards (GxP, 21 CFR Part 11, EMA Annex 11). They develop and execute validation protocols (IQ, OQ, PQ), risk assessments, and doc...
Posted 5 months ago
7 - 12 years
25 - 35 Lacs
Noida, Chennai, Bengaluru
Hybrid
GRC professional with good understanding of industry frameworks and standards 2. In-depth experience on Third-Party Risk Management a. Evaluating third party's cybersecurity control and ensuring they are in compliance with organizations standards and industry best practices b. Track and monitor the status of each due diligence review and communicate the status with management and key stakeholders on a regular basis c. Articulate risks and potential options for remediation or compensating controls d. Understand inherent risk assessment e. Perform new and recurring third party security risk assessments, develop mitigation plans, and work with internal stakeholders to assign remediation trackin...
Posted 5 months ago
2.0 - 4.0 years
3 - 5 Lacs
ahmedabad
Work from Office
Job Title: Junior IT Administrator Bioanalytical Lab Support Experience: 2-3 Years Job Summary: The Junior IT Administrator will assist in maintaining the IT infrastructure and systems used in regulated bioanalytical operations within a GLP/GxP-compliant CRO laboratory. This role involves daily user support, troubleshooting, and basic system administration related to lab instruments, LIMS, and networked IT systems. Key Responsibilities: User & System Support Provide first-level IT support for lab users on desktops, applications, and hardware. Troubleshoot issues with instrument PCs, printers, and lab software (e.g., LIMS, Lab Solution, Analyst software). Ensure timely resolution of support t...
Posted Date not available
3.0 - 7.0 years
4 - 9 Lacs
chennai
Work from Office
Packaging Validation Engineer: Lead and execute packaging validation activities with a primary focus on seal integrity testing for sterile barrier systems. Develop and implement packaging test protocols and reports in alignment with ISTA (International Safe Transit Association) and ASTM standards. Design and perform package performance and distribution testing, including drop, vibration, and compression tests. Collaborate with R&D, Quality, Regulatory, and Manufacturing to ensure robust package designs and validation strategies. Drive root cause analysis and CAPA related to packaging failures. Maintain compliance with applicable regulatory standards including ISO 11607, FDA 21 CFR 820, and r...
Posted Date not available
3.0 - 7.0 years
4 - 9 Lacs
chennai
Work from Office
Packaging Validation Engineer: Lead and execute packaging validation activities with a primary focus on seal integrity testing for sterile barrier systems. Develop and implement packaging test protocols and reports in alignment with ISTA (International Safe Transit Association) and ASTM standards. Design and perform package performance and distribution testing, including drop, vibration, and compression tests. Collaborate with R&D, Quality, Regulatory, and Manufacturing to ensure robust package designs and validation strategies. Drive root cause analysis and CAPA related to packaging failures. Maintain compliance with applicable regulatory standards including ISO 11607, FDA 21 CFR 820, and r...
Posted Date not available
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