With general direction, provide timely guidance to Clinical Science/ Business Units Standards office to interpret data collection requirements into data models of moderate complexity and discuss with Novartis Clinical Data Standards Governance Board for input and approval. Independently, Develop and maintain all standard objects, procedures, templates and views for clinical database management system (such as OC/ RDC, Inform, Rave) using relevant programming languages (SQL, PL/ SQL, C #, VB script, SAS). Support or lead a special project (limited in scale and scope) both clinical and nonclinical in nature. With general direction, Work with the Clinical Science Units to understand the data requirements for collection and submission With general direction, Define the data content and structures for collection, transformation and CDISC SDTM submission requirements in Novartis Clinical Data Standards (NCDS) of moderate level of complexity. With general direction, work with the Data Standards Governance Board to ensure that the data models are consistent with Novartis Clinical Data Standards With general direction, Perform Impact analysis for proposed modifications to existing domains, permitted choices for discussion with Governance. Independently, develop, test and maintain all Global/ Disease level Library objects needed for clinical studies (DVGs, DVG subsets, Questions, Questions Sets and Question Groups) or equivalent in CDMS. Document, Develop, review and maintain Global Library Copy Groups of DCMs, DCIs, Procedures, Views and DCI books or equivalent in CDMS for reuse of standard pages for individual trials. Seek process improvement and incorporation of newly discovered practices towards maintenance of Global Conventions for data modeling/ standards and Style Guide for CDMS implementation. Contribute to the review of global SOPs and business guidance/ user guides directly impacting the function and providing input when applicable. Document, Develop, test and maintain OC validations and derivations procedures using (SQL, PL/ SQL, C #, VB script, SAS) on Global/ CSU/ BU standards. Maintain Form Layout Templates, Extract Macros and Key Templates or equivalent for use in individual trials. Promote study DCM, DCIs and Procedures to the GLIB or equivalent if approved for re use by Governance. Ensure alignment between CDMS Global Library Objects and Metadata Repository. Good Knowledge of Novartis Data Clinical Standards , Data Models and their implementation for database and GLIB development Train less experienced associates on specific tasks relating to Novartis Clinical Data Standards and/ or Global Library Processes Subject matter expert in OC, INFORM and GLIB processes Act as a consultant to CSU/ BU for Novartis Clinical Data Standards and CDMS setup, including procedure development or equivalent. With general Direction, Manage MDR related Tasks ensuring consistency across consuming systems (such CDMS, LSH). Supervise Individual Contributors of External Partners (Contingent Workers, Functional Service Providers, Interns, etc) & Novartis FTE, as required. Exp:1 - 5 yrs Location:Hyderabad
The incumbent must have at least 7 to 12 years in manufacturing assurance, engineering assurance, analytical assurance in formulations.
Exp: 7 - 12 yrs
Patients' Medical Information into standard Diagnosis codes(ICD-10CM) and Procedure Codes(CPT). Requirements: Age should be below 30. Good Communication skill. Benefits- Weekends off/Cab/Food/Incentives
Contact: HR Abinaya - 9952034772
M Tech/BTech equivalent from a reputed College/University with 5+ years of experience Requirement : Expertise in JAVA/J2EE programming language utilizing Spring MVC and Hibernate/JDBC. Experience in working on Multithreaded Systems. RESTful Web Services and exposure to TestNG, JUnit. ExtJs experience will be considered. Strong systems fundamentals related to performance, scale and factors outside the JVM that impact the system. Strong experience with SQL databases (procedures, triggers, etc.) Expertise in Linux and Network programming. Expertise on GIT/Stash and maven.
Exp: 5 - 10 yrs
Walk- In Drive for Sr Fitter & Jr Fitter and electrician Engineering Services Dept . in API Division , Candidate should have 2-7 yrs experience in Job descriptions of the Senior Fitter 1. A H U Preventive maintenance. 2. Formulations equipment's maintenance a) FBP b) RMG c) Compression d) Coating e) Roller compactor and others 3. Facilitating Maintenance 4. Documentation. 2 to 4 Yrs experience Job descriptions of the Junior Fitter. 1. A H U Filters cleaning 2. Equipments maintenance 3. Documentation etc PILOT PLANT J ob descriptions of the Senior Fitter 4 to 7 Yrs 1. AHU Preventive maintenance. 2. Production block equipment's preventive maintenance a) SS reactors b) GL Reactors c) Centrifuges d) vacuum Pumps e)Cooling Towers f). Facilitating Maintenance g).Documentation. 3. Clean room equipment's Preventive maintenance a) Micronizer b) Miller c)Sifter d)RCVD Job descriptions of the Junior Fitter 1. A H U Filters cleaning 2.Shift maintenance works 3. Documentation etc Job descriptions of the Electrician Utility operations a) Chilling Plants b) Nitrogen Plant c)Air compressors d)Single fluid System e)Hot Oil System f) Plant electrical Works , experience , Date of Interview : 22.05.2017 ( Monday ) Interview Time : 9.00 AM to 1.00 PM Venue Details : MSN Laboratories Pvt Ltd, R&D Center, Plot No.12, Phase IV, Sy.No.119 to 140, 258,275 to 280, IDA Pashamylaram, Pashamylaram (V) Patacheru (Md), Medak (Dist) Telangana 502 307, India. Tel No : 08452-304799/4899 Mobile No : 9515115106 Note : Candidate Should carry their resume, 3 months Payslips, Bank Statement and recent Increment Letter, Qualification Certificates .