Jd:
Gathering requirements for PI designing of a product
Liaising with various product (operations, validation) experts and subject matter experts to determine the requirements for the new PI’s desgning.
Designing and developing the master data for equipment management, Inventory management, User management in MES
Design and creation of MBR for specifications on Bill of parameters (BOP).
Design and creation of complex PI’s for Weighing & Dispensing, Manufacturing and Packaging processes.
Site specific requirement analysis for each of the above processes and convert them into Batch Records
Validation of the created PI’s for site deployment
Providing status updates to the Project Manager on a day-to-day basis on progress, issues, and risks.
Work with product vendor on product related issues during upgrade
Troubleshoot and defects resolution during validation of PI’s.
Strong Pharmaceutical, Bio Tech, Manufacturing and Shop Floor Order processes knowledge to convert the site requirements into Batch Records
Experience:
End to end implementation experience of Siemens Opcenter EXPH.
Experience on Siemens Opcenter EXPH modules like User management, PI Management, PI Process, PI Review, Weighing & dispensing, XSI console, Equipment Management, Material Flow management, Weigh & Dispense.
Experience on SAP-MES interface, L2 integrations, report development,
Knowledge of ISA95/S88 standards & practical use of these standards in application design, Knowledge of Pharma manufacturing.
Good Communication and Analytical skills
Hands on Experience in Siemens Opcenter EXPH Specification, Execution, Compliance & Performance Module.
Experience in Siemens Opcenter EXPH- Configuration, Customization
Experience on Siemens Opcenter EXPH Installation, Upgrade, Development and Configuration.
Knowledge of GxP, GAMP, 21 CFR Part 11
#opcenter #seimens #gamp
If interested can forward your updated resume on hr4@tasolutions.in and can directly contact us on 9056679449 also can provide our reference to your friends and colleagues
Key Skills
Must have very good understanding of OAM Architecture and Design
Must have contributed to development of OAM SW(FCAPS/PM/CM/FM/AM)
Must have C++/C Development experience.
Good to have Knowledge of protocols like Netconf, Confd, Yang.
Optional: Knowledge of ORAN including CU S & M-Plane specifications, ONAP.
Optional: Experience with mentoring and leading a team of at least 6-7 engineers
Responsibilities
Development of OAM Features for vRAN/Single RAN Systems
Stabilization of existing OAM blocks for vRAN/Single RAN Systems
Development of features for ONAP / OpenStack / Microservices based vRAN/Single RAN OAM
vRAN SW
#oam #faps #fcaps
If interested can forward your updated resume on hrd@tasolutions.in and can directly contact us on 9056679449 also can provide our reference to your friends and colleagues
JD:
AVEVA OSIsoft PI System Installation, Implementation, Upgrade, migrate and Configuration
Worked on PI Asset Framework and event frames extensively – Hands on
Good knowledge and Experience over the OSIsoft PI-Historian (ProcessBook, DataLink, PI – PI Interface, PI ACE, Rt Reports and Alarms for Batch and process industries)
Install and configure PI OPC Interfaces with failover, Configure PI buffer Subsystem (upgrade and Design)
PI Vision Servers administration, PI Web API Administration and implementation, PI Datalink, PI ProcessBook, PI Vision page development, support, and administration Compliance Activities
User Support as a PI SME
OSIsoft PI Tag creation/update/improvements or troubleshooting in
alignment with customers
Working knowledge of MS SQL Server and/or Oracle/Azure/AWS
Experience in troubleshooting & analytical skills
Experience in customer interaction/client-facing experience.
Effective communication skills (Verbal/written)
Experience in working with onsite-offshore model
Good Exposure to customizing applications using PI SDK, PI AF SDK, Visual Studio .NET, Angular and SQL – Valuable
Experience in the implementation of OSI-PI based systems for the pharmaceutical industry – Valuable
Pharma validation process and documentation (GMP / FDA) – Valuable
Main activities with start by complementing and supporting a European core team:
Roll out of established and validated OSI PI models to multiple sites
Documentation preparation (IQ,OQ and PQ) as part of deliverables
Integration of equipment into OSI PI system via OPC-DA , OPC-UA, PI RDBMS, PI UFL
#osisoft #aveva #opcda #rdbms
If interested can forward your updated resume on hr4@tasolutions.in and can directly contact us on 9056679449 also can provide our reference to your friends and colleagues