Responsibilities The incumbent is responsible for developing and revising quality standards for dietary ingredients/supplements and responding to internal and external queries related to dietary supplements in USP-NF. These activities require the critical evaluation of relevant scientific documents and other information, the performance of literature searches on related topics, and the development and drafting of pertinent documents for other scientific staff and/or Expert Committee review. The incumbent liaises with expert committee members in the critical review of analytical validation data, and other regulatory and laboratory data to assess suitability of proposed methods and reference standards. The incumbent provides technical input to other DSHM scientists. The incumbent recognizes when additional expertise is needed and he/she has the ability to put together and manage advisory panels. The incumbent also closely follows the work in areas of pharmacopeial standards other than dietary supplements so that collaboration and exchange of information is seamlessly accomplished and made available when needed. He/she establishes and maintains relevant contacts outside of USP, stays abreast of new findings, and informs other scientific staff of new developments in dietary supplement quality methodologies. The incumbent may act as a liaison between Expert Committee and interested parties from government, academia and industry on issues pertaining to standards for dietary supplements.    

Resposibilities Co-lead and manage, together with a Product Operations Manager (POM) and a Technology Lead, a complex, globally deployed, high-impact scientific software product in a GxP environment strive for excellence in product management to continuously improve the impact and value of software and data to BR ensure your product contributes to an intentional, integrated, and capability-based software product architecture and continuously increases the value defined by the strategic mandate of your Product Line ensure adherence to Novartis global Information Security and Quality standards and policies for all products/services ensure regulatory compliance (e.g. GLP & GCP) standards and policies for GxP products/services is adhered   Qualification & Experience Bachelor's degree or equivalent experience in a life science, computer science, engineering or information technology discipline. 15+ years experience in managing software products in a lifescience environment (ideally pharmaceutical research) PhD in a life sciences discipline, scientific informatics or equivalent experience At least 5 years experience in people leadership  

Quailification & Experience Any Graduate or MBA 2 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 Diploma in Endoscopy 2 to 3 years of experience   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Business development and marketing of APIs to Generic Pharmaceutical Companies in domestic, emerging markets and EU markets for a few products. Finding and selecting new Customers, distributors, and agents in the concerned market. Playing a significant role in planning the strategic road map of the organization by setting up a product selection process in the company and, designing the product pipeline and prioritization for planned future.   Qualification & Experience 5-7 years for Assistant Manager and 8-10 Years for Manager. Experience of sales, business development or corporate strategy in Pharma industry is required B.Pharmacy/ M.Pharmacy/ MBA  

Qualification & Experience M.Pharm / B.Pharm / M.sc 2 to 6 years of experience   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Core scientific member of cross-functional franchise team and a disease area expert, responsible for scientific foundation of Therapeutic Area (TA) medical strategy. Conceptualization and project management of wide range of medical activities (including research, publications, medical education, patient support programs, advisory board meetings etc.) that are aligned to the TA Medical strategy. Engagement of identified key thought leaders through medical affairs activities, in alignment with the overall strategic plan. Responsible to ensure optimal execution of strategic medical affairs plan through Regional Medical Affairs including but not limited to medical education, product education, medical evidence generation, advisory boards, pre-license activities and special projects. A therapeutic area scientific expert, responsible for discussing the scientific data pertaining to products on proactive and reactive basis, patients’ treatment trends and studies in the therapeutic areas in which the Company is involved, with defined audience of leading specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other Stakeholders) and to be considered a trusted scientific counterpart Responsible for devising optimal training plan to ensure flow of latest medical developments in the given to sales & marketing team Jointly responsible with therapy area lead to support optimal patient outcomes through communication of data, information, knowledge and insights in support of healthcare professional needs and organizational goals Representing the organization in various internal & external scientific platforms Responsible for development of Medical Affairs strategic plan for identified TAs and products Ability to convert insights on disease trends and treatment patterns from key thought leaders into viable and formidable strategic plans to shape the therapeutic areas of interest Responsible for identifying knowledge gaps, practice gaps and data gaps and develop strategic medical actions plans including but not limited to medical education, product education, evidence generation and special projects Collaborating with thought leaders to conduct therapy specific reviews, meta-analysis, case studies, case series, patient reported outcomes and publish them in journals of repute Receiving and processing scientific information requests received from physicians Ability to handle complex questions from health care professionals related to GGI products or disease area to satisfaction Ensure that all activities in the TA are conducted in alignment to Dr. Reddy’s COBE (Code of Business Ethics) Policy and compliance guidelines Responsible for ensuring that all promotional, physician and patient education materials are approved within stipulated timelines and in alignment with Dr. Reddy’s Promotional Material approval policy Product pipeline champion with an ability to identify unmet needs through active stakeholder interactions and actively contribute in the new product ideation and development of differentiated products   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities People: (1) Maintain effective relationships with the end stakeholders within the allocated GBU and product – with an end objective to develop education and communication content as per requirement for HEVA communications; (2) Interact effectively with healthcare professionals on publication content; and (3) Constantly assist other writers (junior) in developing knowledge and sharing learning Performance: (1) Create HEVA communications deliverables (including manuscripts, posters, abstracts, and slide decks) aligned with HEVA strategy and global HEVA communication plan across relevant business units and product teams as per agreed timelines and quality; and (2) Provide strategic support with individuals and institutions, which may serve as resources for publications purpose, etc Process: (1) Develop complex publications material; (2) Act as an expert in the field of medical communication for the assigned therapeutic area; (3) Assist the assigned scientific communication team in conducting comprehensive publication-needs analysis; (4) Manage core HEVA communication processes, templates, and products across the portfolio in accordance with the scientific and value messages aligned with Core Value Dossier, the US AMCP Dossier, and HEVA contributions as appropriate to other submissions; (5) Ensure Core Value Decks for key products are established and maintained, making available a regularly updated synthesis of critical HEVA evidence on the value of products; (6) Maintain accountability for adherence to the publication SOP and other compliance expectations relevant to HEVA communication processes; (7) Maintain accountability for adherence to the publication SOP and other compliance expectations relevant to HEVA communication processes; (8) Implement relevant element of publication plan and associated activities for the year identified for the region; (9) Work with selected vendors within the region to deliver the required deliverables as per defined process; and (10) Design an overall plan of action based on end-user feedback and improve course content and delivery Stakeholder: (1) Work closely with HEVA global and local teams, RWE global and local teams and scientific communication teams in regions/areas to identify publications needs and assist in developing assigned deliverables; and (2) Liaise with HEVA global and local teams to prepare relevant and customized deliverables     Qualification & Experience Experience: >4 years of experience in content creation for the pharmaceutical/healthcare industry, or academia Soft skills: Stakeholder management; communication skills; and ability to work independently and within a team environment Technical skills: Relevant training/experience in health economics, public health, epidemiology, or other relevant health-related scientific discipline (including but not limited to therapeutic area/domain knowledge exposure; knowledge of Good Publication Practice; publication submission; and/or project management) Education: Advanced degree in life sciences/pharmacy/similar discipline or medical degree  

Responsibilities Maintain effective relationships with the end stakeholders (Medical scientific community) within the allocated Global business unit and product – with an end objective to develop medical information content as per requirement. 2) Interact effectively with stakeholders in medical and pharmacovigilance departments. 3) Constantly assist other medical information writers in developing knowledge and sharing expertise. Performance: 1) Provide SME support and high-quality completion of deliverables (local and custom scientific response documents, US FDA Annual Reports, and Compendia Reviews) as per agreed timelines and quality. 2) Supports delivery of projects in terms of resourcing, quality, timeliness, efficiency, and high technical standards with the agility to learn and contribute to situations of demands. 3) Ability to multi task and manage different type of projects simultaneously. Process: 1) Act as an expert in the field of medical information writing with project management skills and maintain the regulatory requirement for countries supported. 2) Assist the assigned medical information team in conducting comprehensive medical writing needs analysis. 3) Implement relevant elements of content plans and associated activities for the year identified for the assigned countries. 4) Work with selected vendors within the region to deliver the required deliverables as per the defined process. 5) Design an overall plan of action basis end-customers feedback & improve course content and delivery. 6) Capable of identifying risks to processes and proposing mitigation plans through the application of a problem-solving mindset. Stakeholders: 1) Work closely with medical teams in countries/regions/areas to identify medical writing needs and assist in developing assigned deliverables. 2) Liaise with the Medical department to prepare relevant & customized deliverables. 3) Collaborate with the Global Medical Information team and country medical information teams as relevant.     Qualification & Experience Education: Advanced degree in life sciences/pharmacy/similar discipline (Ph.D., Master, or bachelor’s in science, D Pharms) or medical degree (MBBS, BDS, BAMS, BHMS, MD) Experience: ≥8 years of experience in content creation in medical or scientific writing for the pharmaceuticals/healthcare industry, or equivalent experience in the clinical setting, pharmacovigilance; At least 4 years of direct medical information writing experience in the pharmaceutical company; Minimum 2 years of experience in managing global, cross-functional project teams, working in a Matrix environment, and acting as an SME, mentor or guide. Soft skills: Excellent communication skills (written, verbal, and presentation), Stakeholder management; and ability to work independently and within a team environment.  

Responsibilities Carry out Formulation and process development activities on differentiated formulations and innovative technologies to achieve Product development with adherence to timelines. Carry out & support Process development for R&D and pilot scale to achieve Product development with adherence to timelines. Carry out & support Late-stage development of differentiated products for LBOE India & Global LCM and support their regulatory filing. to achieve Derive a stable formulation and scaleup to commercial. Establishing design space and derive the CQA & CPPs to achieve a reproducible product and process. Scale up activities by providing the scale up factor/suggesting the appropriate methodology, Identifying the optimum process parameters for commercial batches based on trends observed in first few commercial batches to achieve. Coordinate with CROs and CMOs for the external development of Projects and for IMP supplies to achieve Timely completion of projects in line with the requirements. Carry out Subject Matter Expertise in defining and execution of complete strategy for product development for complex injectable dosage type, identifying critical CQA for structural & physiochemical parameters to achieve Product development with adherence to timelines. Carry out & Support Trouble shooting in CMC related activities and adequate investigation, identification and rectification of problem to achieve Product development in compliance to quality systems. Support Delivery of Project defined Deliverables including plans, meeting budgets and status reports to achieve Provide regular updates and ensure that the project meets budget and defined timelines. Carryout & Support Writing and Review of protocols, reports, validation plans and development report to achieve Product development in compliance to quality systems. Carryout & Support Developing, maintaining, and upgrading FHPDC facility to achieve Support the facility team to maintain and run at FHPDC site. Support Stage gate clearance for product development, with special attention to regulatory and intellectual requirements to achieve Product development. Carryout/ Process optimization with special focus on QbD aspects of drug product development to achieve Product development.   Qualifcation & Experience M. Pharm/Ph.D from premier institute. At least 7-9 years of industrial research experience, in the field of formulation development for differentiated products/ 505 B2 products/generics (Injectable dosage form) for global markets including Scale up and Tech transfer experience.