Qualification & Experience B.Sc/M.Sc Nuclear Medicine 2-5 Years of experience   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"

Responsibilities Collaborates closely with global medical affairs team to ensure quality and timely medical contribution for key strategic submissions such as new applications, renewals, variations, etc. Contributes to the creation of medical documents dedicated to Health Authorities and other national authorities. Conducts rigorous analysis of medical/scientific data and participates in the elaboration and/or the evaluation of their publication. Presents and drives the preparation for clinically driven topics for assigned non-core CHC portfolio in front of Governance Committees Monitors medical news and publications, shares key learnings/alerts to global medical affairs and maintenance team Facilitates internal medical trainings on CHC-relevant therapeutic areas and disease pathologies. Reviews and approves promotional and non-promotional communication materials for non-core CHC portfolio. Provides scientific monitoring oversight activities of medical vendors Proactively identifies and communicates to higher management potential medical risks and options for issue resolution (e.g.: maintenance issues, submissions, etc.) Follows CHC governance, ensuring Sanofi/industry standards are maintained at all times while looking for opportunities to streamline processes in the future Ensures ethics, transparency, quality, and compliance of all medical activities (internal policy, procedures)   Qualification & Experience Medical or Pharmacy Degree. Scientific/health related degree (PhD, Phar.D.) is acceptable if supported by good experience. At least 3 years of relevant work experience in Pharmaceutical Industry and/or in Consumer Healthcare is a real asset  

Responsibilities Identify and drive system or process changes to enhance data quality, user experience and compliance. Provide guidance and support for related initiatives, including system upgrades and enhancements in support of regulatory processes and obligations. Monitor system performance and ensure that performance or capability issues are resolved effectively. Partner with IT colleagues on system implementation and change control activities, including development of iQMS IT quality documentation to support user acceptance, including test scripts and reports. Support in managing the design, validation and delivery of regulatory reports for compliance and dept. KPIs. Ensure timely delivery of ad-hoc and regular reports. Ensure capture of high data quality regulatory data. Identify and communicate data errors and inconsistencies, and drive data remediation initiatives as required. Manage the delivery of compliance reports required to support business stakeholders. Delivery of effective system user training and system access promoting compliant use of RIMs application. Ensure up to date process documentation, training materials and user guides. Provide Systems Administration, including management of user access and roles. Provide day-to-day support to the users. Champion the importance of registration tracking within the organisation through regular communication with global stakeholders. Support as necessary other activities related to Systems team   Qualification & Experience Bachelor’s degree (or equivalent experience) 2 years’ experience in regulatory operations (or similar) role Experience within pharmaceutical organisation, in particular Regulatory Affairs. Understanding of global regulatory affairs processes Familiarity with the range and types of non-prescription healthcare products, including over-the-counter (OTC) medicines, cosmetics and devices.  

Qualification & Experience B.sc / M.sc In Nursing 3 to 5 years of experience from any reputed hospital   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"

Qualification & Experience Work Areas: Operation Theatre (Neuro/CTOT / GOT/ Labour Room & Wards) Minimum 1-7 years with any hospital. GNM/B.Sc (Nursing) with Registration   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities The Neurosurgeon will be responsible for diagnosing and treating disorders of the nervous system, including the brain and spine. Day-to-day tasks may include performing surgeries, conducting diagnostic tests, evaluating patient conditions, prescribing treatment plans, and collaborating with other healthcare professionals.     Qualification & Experience Specialization in Neurosurgery and/or Spine Surgery Experience in diagnosing and treating neurological disorders Expertise in conducting surgical procedures related to the nervous system and spine Knowledge of neurology and neurosurgical techniques Excellent problem-solving and decision-making skills  

Responsibilities Responsible for generating Business in allocated territory (Nutraceuticals and Dietary supplements) B2B Business Development (Contract Manufacturing and ingredients) - Generating Business from new as well as existing clients in India and International Should have exposure in nutraceutical domain & dietary supplements. Client Coordination, Business Development, Finalizing products, planning orders in India and International Interact with the productive and lucrative marketing sources for the business Upgradations and maintenance of website Market Research, Identifying Specific Markets and Formulating Strategies. Developing and maintaining relationship with the clients. Responsible for getting new leads and maintaining existing clients to enhance business relation Prepare customer database, calling maximum clients and presenting company on regular basis and handling turnkey projects. Prepare market survey, prepare SWOT, and make strategies Prepare data for company information in form of brochure, leaflets, presentation & pamphlets. Work independently and multitask in a fast-paced environment Co-ordinate with standard team for new product development, market and sale the existing standard product Preparing technical offer and maintaining customer relationship     Qualification & Experience M.B.A in Business Operations or Any PG in Science Experience: 12 to 15 years   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Day-to-day office operations support, including oversight of cleaning, amenities, office hoteling processes, conference rooms, workspace setup and onboarding, always ensuring a high standard of service. Assist internal customers (colleagues) with all Workplace Services related items. Organizing and Hosting parties / events on special occasions. Employee logistic Management. Maintain office equipment, office supplies, and restocking pantry areas as needed. Ensuring issues are proactively found, allocated, prioritized, and fixed with efficiency. Keep trackers and management systems up to date and produce reports the WPS team and other support teams when required. Create and maintain access logs and badges using the access control system Assist with the procurement, administration and coordination of Workplace Services including coordinating team and project POs.     Qualification & Experience Bachelor’s degree or equivalent work experience Minimum of 5 years of experience required in Facilities Experience working within a customer-facing environment Experience with planning and scheduling of maintenance activities is preferred, but not required Experience in pharmaceutical industry is preferred, but not required  

Responsibilities SharePoint Maintenance Activities; Support GRT member transition by setting up transition form Liaise cross-functionally to generate periodic internal milestone report Performs simple analyses as directed Support planning and managing timely deliverable of critical regulatory deliverables (registration samples) and various Module 1 documents for ex-US,ex-EU countries Request certificates from respective Health Authority (FDA, EMA, Swiss Medic) and manage notification process Shipping of documents, as required Admin- scanning, copying, shipping label Product Divestiture: Upload relevant documents into the Virtual Data Room (VDR) for potential buyers Product Deletions: Gather information from the Country Regulatory Managers for Product Deletions Strategy Tracks deletion notifcations to country Reg HA Asset Integration: Upload incoming documents to the BMS systems, ensure correct update of meta data; Remediation of documents, as directed Schedule RRT meetings and communicate timelines Set up response templates to ensure submission readiness Submission of responses for publishing Support preparation of GRS analytics and monthly dashboards, eg submission, Approvals, key achievements, miles stones     Qualification & Experience Minimum of a Bachelor degree in a Natural Science, Pharmacy, or other Healthcare-related field 0- 2 years in pharmaceutical industry  

Responsibilities In consultation with GRM TA Lead or designee, support the implementation and management of RMPs and related aRMMs/APVAs, as required: Support The Management Of RMP And Related ARMMs/APVAs (e.g. Global, Regional And/or Local Commitments) Implementation And Associated LM And REMS Collaborations, Including But Not Limited To: Complex aRMMs (i.e., Pregnancy Prevention Programs, Controlled Distribution Programs, etc.). aRMM direct import (DI) activities (i.e., coordinate and monitor DI vendor website and associated alerts). Business agreement changes (in-licensing/Pharmacovigilance Agreements) that impact RM. Additional RM Related Activities Include But Not Limited To: GRM related training management (i.e. planning/tracking/repository) in collaboration with PV Learning Strategy function. aRMM effectiveness related activities (i.e., manage data acquisition, etc.). Ongoing GRM TA Regulatory Information Management system (Verity) related tasks for RMPs and aRMMs, including process improvements (i.e., Verity User Guide/User Requirements and associated work instructions). Track budget spend and monitor vendor key performance indicators, as needed. Maintenance, tracking and support repository of all materials and queries related to above. Support GRM TA Lead with RM related Non-Interventional Research (NIR) activities (global and/or local). Support GRM TA Lead in managing, collating, and access of LM RMP related queries from Local Health Authorities (HAs). Support other innovative projects to further RM related intelligence and efficiencies (i.e. HA RM related queries and other RM initiatives such as functional endorsed AI tools/platforms, new collaborative methods, etc.). Maintain inspection readiness and participate in audits and inspections related to GRM. Support GRM TA processes and procedures working in conjunction with GRM TA, GPO/GPL (as required). Support the development and maintenance of RM-related SOPs, WIs, metrics, quality checks in close collaboration with GPO/GPL and GRM SOE. Maintains a thorough understanding of RM regulations and industry trends. Other responsibilities as assigned by GRM TA Lead.     Qualification & Experience Advanced scientific degree preferred More than 3 years of relevant pharmaceutical industry experience Experience in global pharmaceutical safety risk management is preferred Understanding of pharmacovigilance/regulatory environment is expected