Provides production support, including researching and resolving problems, unexpected results, or process flaws performing scheduled activities recommending solutions or alternate methods to meet requirements. Serve as the primary point of contact for all operational support issues related to ServiceNow. Manages projects/process improvement, including applying change management experience to facilitate movement to new levels of quality. Identifies and understands issues, problems, and opportunities. Compares data from different sources to draw conclusions. Uses effective approaches for choosing a course of action or develops appropriate solutions. Takes action that is consistent with available facts, constraints, and probable consequences. Uses data to build project plans and ensure adherence to schedule and other specifications. Utilizes interpersonal skills when working with various customers and peers to accomplish project goals. Recommends process/customer service improv

ROLE AND RESPONSIBILITIES · Build a strong network with professionals like doctors, chemists, stockiest and distributors. · Analyse market trends and conditions to understand where opportunities for networking and business-building may arise. · Ensure that client servicing facilities are carried out in an effective, timely and efficient manner. · Reach out to doctors and other medical professionals through both offline and online means and develop constructive relationships. · Knowledgeable about the product offerings, services and unique benefits provided by competitors and other relevant companies. · Be a regular part of medicine-related events and take advantage of networking opportunities. · Accurately document and record the proceedings with each client and report back. · Introducing new items to the marketplace · Product Promotion and Customer Reaction to the Product in the Pharma Industry · Medical representation is in charge of company representat

Handle Inbound calls from US Customers and provided real time assistance Handle customer queries and provide resolution Perform Troubleshooting steps with customers over the phone and provide resolution Create Tickets/Truck Rolls for issues not resolved over the phone Perform TSR on the calls

We are searching for an innovative, well-organized MIS executive to join our company. The MIS executive's responsibilities include designing and developing computer systems on time and to specifications, developing strategies, keeping up-to-date with the latest developments in IT systems, analyzing operations, and making suggestions for improvement. They also allocate resources, as well as assist with training and onboarding. You should be able to effectively manage risks and also protect data.

Requirement Analysis for Testing Test Case Writing Test Case Execution Defect Life Cycle Status Reporting Testing Artifacts Repository Supervision of Software Testers Review of software requirements Preparation/review of test plans Preparation/review of test cases Execution of tests Reporting of defects Preparation of test reports

Responsibilities • Your primary role would be to ensure effective Design, Development, Validation and Support activities, to assure that our clients are satisfied with the high levels of service in the technology domain. • You will gather the requirements and specifications to understand the client requirements in a detailed manner and translate the same into system requirements. • You will play a key role in the overall estimation of work requirements to provide the right information on project estimations to Technology Leads and Project Managers. • You would be a key contributor to building efficient programs/ systems and if you think you fit right in to help our clients navigate their next in their digital transformation journey, this is the place for you

Your responsibilities will include Writing effective and scalable Python codes Designing and implementing robust applications Debugging applications to ensure low-latency and high-availability Integrating user-facing elements with server-side logic Implementing security and data protection Accommodating various data storage solutions

JOB DESCRIPTION You will be responsible for preparing and reviewing technical documents for ANDA/dossier submissions in various countries. You will need to format these documents according to CTD, ACTD, and country-specific guidelines and coordinate with other departments for any necessary technical or administrative documents. Additionally, you will be responsible for creating clear product labels and patient information leaflets, coordinating with the Drug Control Authority to obtain manufacturing licenses, and ensuring timely filing of variations and following up for approvals.

FRESHERS ARE WELCOME. Job Responsibilities HCP management through scientific support for CMEs, conduct of Clinical research (Post-approval observational studies), support for medical information queries, literature review for scientific updates, capture KoL insights with conduct of Knowledge, Attitude, and Perception survey Non-interventional studies Develop study documents for site initiation, monitor and closeout of Phase IV Post-approval observational studies Communication material Development and review of promotional literature, activities, scientific support for key brands and new product launches including product monograph, training manuals, FAQs, LBLs and Publications Training Provide training for New Induction executives Conduct Product updates during CBM, Questionnaires, Direct mailers for In Clinic effectiveness Regulatory support Preparation of prescribing information, rationale for New product proposal or evaluation Corporate Academic Initiati

1) Literature search and design of CT (patient based PK/PD end point studies) 2) Preparation of CT study synopsis, including sample size calculation 3) IMP calculation for Clinical trials 4) Clinical trial monitoring (In process, risk based) 5) Investigational products management 6) Oversee Clinical trial s execution with the help for CRO at hospital sites 7) Center point contact for CRO and internal stakeholders 8) Well understanding of CT related guidance focusing on FDA guidance 9) Understanding the CT (PK end point, PD endpoint) studies data evaluation and report review 10) Controlled correspondence, scientific justification authoring and review

Roles and Responsibilities 1. Should have knowledge of method development and analysis of Mass, IR and UV-Vis spectroscopy, HPLC, GLC 2. Knowledge in quantitative and qualitative analysis must. 3. Sample preparation, operation of sophisticated analytical equipment such as HPLC, GC, spectro photometer etc 4. Documentation of data in analytical format to interpret result 5. Making qualitative and quantitative data analysis of required or provided sample to get idea of progress of project. 6. Produce result in reproducible 7. Produce result from wet lab analysis 8. Troubleshoot analytical procedures or equipment in case of any typical observations/data/results being identified during sample analysis or performance check. 9. Staying updated of the up-to-the-minute technical and scientific improvements 10. Produce data with accuracy and precision. 11. Excellent communication skills must be able to communicate with individuals at all levels of organization

Health advisers have more responsibility than service advisers. They provide assessment, basic health advice and information to patients, supporting them to access the appropriate care, including advice to manage their symptoms at home.

PURPOSE Lead for vaccine process development, scale the function in accordance to the divisional requirements Thorough understanding of regulatory and GMP regulations and critical quality attributes for Vaccine Development With the objective of developing the processes for vaccines and tech transfer for manufacturing and licensing AREAS OF RESPONSIBILITY (AOR) Direct the overall activities of the upstream process development "• Conceptualizes the overall plan and goals for the function • Develops long term / short term implementation plans for the function in line with PD, CD and program strategy • Guide the design and development (protocol, execution, reporting, and approval) of vaccine process which meets the global expectations by anchoring the functional reviews. • Guide the function in order to create scientific reports of global quality and as per regulatory standards • Provide technical direction and guidance to team IN ORDER TO deliver optimal resu

Typical duties of a marketing executive include contributing ideas to marketing campaigns conducting research and analysing data to identify and define audiences compiling, distributing and presenting ideas, information and strategies coordinating promotional activities, events and interviews managing production and performance of multimedia content writing and proofreading creative copy maintaining websites and tracking data analytics updating databases and using a customer relationship management (CRM) system monitoring budgets managing social media campaigns monitoring performance of marketing campaigns.

Do you have sense of urgency, ability to manage and prioritise multiple work requirement to meet deadlines Are you flexible and enthusiastic to go beyond the given instructions to create business value If so, Novo Nordisk awaits your application as Associate Power BI Analyst. Apply today and join us for a life-changing career. About the department Global Finance GBS Bangalore was established in 2007, is currently responsible for supporting Accounting, Finance Procurement, Financial Planning Analysis (FP A) for Headquarters, region Europe, North America, International Operations (IO) GBS Bangalore. The main purpose of our existence is to provide superior service to our stakeholders consistently and add value to the processes in terms of standardization and efficiency. The Position As an Associate Power BI Analyst in BI COE team, Finance GBS FP A team you will participate in financial system operational activities in Novo Nordisk with a close link to Product supply

The CMC Regulatory Specialist has the responsibility to support new product approvals, existing product renewals, and post-approval changes for global registrations, through document distribution and internal database maintenance. This includes supporting the registrations of Lilly products sourced from the US and/or contributing MSRAs, for both Lilly and contract manufacturing sites, to the global marketing affiliates. In this role, the Specialist works closely with Indianapolis regulatory product representatives providing guidance to them regarding the regulatory documentation, reporting requirements and registration processes in global markets. In addition, the Specialist maintains post-approval commitments for products supported from ISRA for both Lilly and contract manufacturing sites. In this role, the Specialist works closely with Indianapolis regulatory product representatives providing essential CMC commitment information and approval status in global markets as part of manufa

Roles and Responsibilities Serve as a Data Operations Coordinator (DOC) for one or more protocol with less than 5 operations . Manage delivery of projects through full data management study life-cycle. Perform comprehensive data management tasks including data review, writing and resolving data clarifications. Develop and maintain good communications and working relationships with CDM team. Desired Candidate Profile Required hands on industry experience in Clinical trial phased and Core DM activities like clinical study startup, conduct, and close out in a Pharmaceutical or CRO's. Perks and Benefits Has the potential work as DTL/LDM on Global Data Management Project Get the chance to work in different therapeutic Areas.

Only need for a mobile phone and hood internet connection