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.    

Responsibilities Visit Doctors, Pharmacists and Hospitals in order to inform on products according to the marketing strategy and with the frequency and number of impacts approved for each segment of doctor. Build up and maintain a relationship with these stakeholders. Assist to Scientific congresses determined by the company. Classification of doctors and other stakeholders of the area according to the segmentation and targeting criteria. Proposal of new doctors to add to the files, changes or removals. Track the prescription habits of the doctor, check his/her consideration of our products, ensure which is the prescription potential and his/her influence in other doctors. Inform in an accurate, updated and according to the company's strategy about our products: use of marketing material, clarification of doubts and concerns of doctors about the products, opposition to objections, advantages compared to the competency. Ensure that other departments complete this information to the doctor if necessary. Obtain information from the market about the doctors' concerns on our products, the competence and test our own marketing strategy and materials. Obtain information about possible public tenders, launchment of competence products, cost containment measures, Health authorities possible instructions to doctors… Transmit this information. Propose activities in their territory (invitation to congresses, participation of doctors as lecturers, organization of clinical sessions…) that helps to promote our products always in compliance with ethics standards and ensuring the Return on Investment. Organize the proposals approved according to the budget assigned. Manage the budget assigned ensuring the return of investment Inform timely and in manner about the daily activity and the next weeks planification and present on time expenses report or any other requested by the company.     Qualification & Experience University degree or equivalent is preferred Background in Science, biology, medical and pharmacy is preferred Proficiency in computer skill Good communication skill  

Responsibilities Integrated Insights Manager will be a strategic partner for a global brand across Novartis divisions and geographies; helping them shape commercial strategies based on robust analytics and data driven insights also would need to collaborate seamlessly with other functional teams within NBS CONEXT's such as (but not limited to) Forecasting, Business Analytics, Primary Market Research, Competitive Intelligence Provides strategic insights to Global Program Team (GPT)/Global Brand Team (GBT) to that shape/develop program/brand strategy. Brings deep understanding of therapy area, market and partners (e.g. patients, ECPs, payers, and regulators) Integrates research, intelligence and analytics to generate insights that facilitates decision making Leads or actively participates in key processes like Strategic Planning, Budgeting etc. Supports key development decision points (DDP, FDP) with relevant commercial assessments Facilitates planning and execution of insights activities in line with brand/ portfolio strategy in collaboration with other NBS functions ensuring high efficiency and quality Brings localized insights into Brand / Program strategy by collaborating with Regional/local teams. Ensures compliance to key Novartis processes (POP-PSP, etc.) across all activities.     Qualifications & Experience Master’s / Bachelor degree in Pharmacy / Science / Medical is essential and with MBA is preferred Candidates with minimum 7 +years of experience in Brand Management , Consulting experience acquired at pharmaceutical companies and /or strategic, marketing, or health care consultancy companies. Superior analytical skills – high comfort in using tools (eg Excel) to analyze and visualize data via standard tools/charting methods Self-Driven and has ability to effectively present and defend analyses Project Management Excellence in facilitation of international, cross-functional teams within a high matrix environment Proven teamwork and collaboration skills. Ability to manage multiple partners / projects Takes initiative to drive standardization of reports across brands  

Responsibilities Ensures effective coordination and collaboration with GRS-CMCs and the regional regulatory leads to ensure key submission deliverables for the assigned projects to the team. Responsible for end to end CMC contribution for the assigned projects; Reviews the assigned regulatory activities including the related technical/supportive information/ documents for completeness and accuracy; Responsible for development of initial global regulatory strategy while considering registered content and seeks endorsement by the GRS-CMC; Responsible for authoring and/or compiling Regulatory Strategy Documents (RSD) where needed; Responsible for authoring of CMC content in Module 1, Module 2.3, M3.2.S/P/R as agreed upon with the GRS CMC within agreed timelines. Responsible for identification and communication of identified risks to the GRS CMCs and/or appropriate leadership, also proposes mitigation strategy with the support of team lead; Ensures resolution of issues and manages regulatory risks within project. Reviews and applies pertinent global regulatory guidelines. Exhibits technical / functional expertise and provides strategies on regulatory requirement, negotiates with and influences the cross functional teams, colleagues and external partners to ensure regulatory data requirements are met. Coordinates with the respective team for M3.2.R Ancillary documents Represents HBU GRA CMC point of view and meets with key stakeholders to resolve challenges. Coordinates internal document review and sign off. Utilizes Pfizer’s CMC systems, i.e. GDMS, PDM, SPA, etc, as appropriate. Supports Query and/or commitment management in collaboration with GRS CMCs. Maintains conformance systems maintenance in support of the GRS CMCs

Responsibilities Committed to quality and excellence in compliance and conformance. With the reasonable understanding of Regional Regulations, would perform the evaluation of the notifications assigned. Accountable for maintaining the RA status in corporate change and dossier management system for the allocated Regions / Markets Contributes independently and manages own time to meet the timelines. Work in collaboration with GRA colleagues to ensure the gaps are identified and escalated on time. Independently Perform accurate updates in system for most of the cases and consult with TL/Designee for clarification of any discrepancies in complex cases, before updating the system. Makes informed decisions on straight cases within guidelines and policies Operate in line with internal SOPs and policies Escalate any potential compliance issues to management Support periodic and ad-hoc system reports to estimate metrics Assist in remediation activities     Qualifications & Experience Bachelor's Degree Demonstrated experience Proven ability to consistently deliver to time, cost and quality standards Operational knowledge of hardware and software tools required for the job Excellent organizational skills and attention to detail Knowledge of documentation practices Fluent in English, verbal and written Project Management experience Knowledge across multiple therapeutic areas

Responsibilities Functions as the Global Product Owner (GPO) or supports a GPO for Life Cycle Management (LCM), working with Cross-Functional Teams (CFT) to prepare regulatory submissions for US, Europe, Canada, Australia and ROW Countries. Responsible for the preparation and finalization of Global Regulatory Strategy Documents (GRSD), CTD sections of supplements / variations for LCM submissions and ensures effective data presentation and quality, by self or under guidance. Responsible for effective coordination with the cross functional teams, site and Global RA teams for the review and finalization of  supplements  to ensure effective data presentation and quality. Responsible for effective review and providing timely feedback to the teams on technical documents including batch documents related to submission (batch records, Exhibit batch and stability protocol). Provides regulatory assessment and supports Change Control Assessment, by self or under guidance. Ensures commitments (module 2-5) made to health authorities are entered into tracking systems and are tracked to closure, as appropriate. Provide regulatory support for the assigned products, participates and provides inputs in technical reviews and Change Control reviews as assigned.   Identifies and assesses regulatory risks associated with assigned projects and timely communication to the team to quickly mitigate the risks. Drives resolution of issues. Communicates issues, impact and outcomes to global regulatory management, Team lead and core team. Remains knowledgeable about current regulations and guidance, interprets and implements in the assigned projects. Responsible for ensuring compliance to Company’s submission standards, policies and procedures.     Qualifications & Experience Bachelor's Degree 3+ years of demonstrated experience in regulatory affairs or in a regulated industry Proven ability to manage complex regulatory issues and consistently deliver to time and quality standards In-depth knowledge of the current health regulatory framework for drug regulatory procedures Problem solving skills, strong detail, quality and compliance orientation Good verbal and written communication skills and fluent in English Proficient computer skills, e.g. MS Office, MS Outlook, Internet, database use Master's degree Relevant pharmaceutical experience Strategic thinking with good project management skills  

Responsibilities To craft and drive the Enterogermina Brand strategy for India with complete responsibility of creating the Integrated Brand Plan, delivering on Marketing Calendar and managing the A&P investments. To build the Enterogermina Innovation pipeline, work with relevant stakeholders to commercialize NPDs, launch and successfully scale up the NPDs To create and drive the probiotic therapy building initiatives among doctors and consumers. To be responsible for the market share, Sales growth and profitability for the portfolio in India Develop a Marketing calendar to drive the strategic priorities of the Brand. Manage the A&P budget for the Brand to ensure strong ROI and optimal spend across key marketing interventions. Design effective and innovative integrated marketing campaigns for consumers/ HCPs across mediums - In clinic, Ex clinic, Digital, Mobile, Print, Radio etc. and flawlessly execute them. Monitor competition on various aspects such as new offerings, pricing, consumer offer, ATL/BTL/TTL activities and course correct strategy if required by periodic travel to different geographies  Conduct intense consumer research directly and through third party to constantly generate insights that can be applied to creative campaigns, product ideas or even on-ground changes Liase with Internal stakeholders (sales force, Industrial Affairs, Regulatory, Medical etc.)  to ensure timely execution and price increase, margin improvement programs and External stakeholders (Creative, other Vendors) to ensure timely execution of New Product Development projects Conduct consumer immersions and understand the key insights pertaining to probiotics. Leverage the insights into an actionable communication strategy. Deliver the communication on the right channels across mass media, digital, in-clinic Work with relevant stakeholders to develop the products for commercialization as per global brand architecture Develop, execute, and monitor business plan for the new products development.     Qualifications & Experience A total experience of 5+ years in the Sales and Marketing Function of a large Pharmaceutical Organization. Preferred industry experience Pharmaceuticals Product / Domain Knowledge Knowledge of the latest trends in Marketing Understanding of the domestic Pharmaceutical Industry. Field experience of up to a year would be preferable. Basic Financial Management Knowledge Analytical ability including computer application knowledge. (MS Office, Data Warehousing, Database software) Graduate in Science/Pharmacy Post Graduate Degree in Management, with a specialization in Marketing for a top management institute Proven track record of managing all aspects of a successful product throughout its lifecycle Proven ability to develop product and marketing strategies and effectively communicate recommendations. Skilled at working effectively with cross functional teams in a matrix organization Excellent written and verbal communication skills Adept at Microsoft – PPT, Excel, word The role is responsible for working within Sanofi CHC, India The position is based in the Corporate Office, Mumbai and requires extensive traveling across the country. This position will suit an individual who is able to operate with discretion and confidentiality about sensitive data

Responsibilities People: Maintain effective relationship with the end stakeholders (medical scientific community) within the allocated Global Business Unit and product – with an end objective to develop education and communication content as per requirement; Coordinate with Project Specialist and Project Managers to lead and develop SGH operation activities; and Ensure new technologies are leveraged Performance: Ensure publication/medical education materials (slide decks, abstracts, posters, and manuscripts etc.) are delivered, stored as per agreed timelines and quality; Develop tools, technology, and process to constantly improve quality and productivity Process: Support delivery of projects in terms of resourcing, quality, timeliness, efficiency, and high technical standards for deliveries made by the medical writing group, including scientific documents and clinical/medical reports; Contribute to overall quality enhancement by ensuring high scientific standards for the output produced by the medical writing group; and Secure adherence to compliance procedures and internal/operational risk controls in accordance with any and all applicable regulatory standards Stakeholder: Work closely with scientific communication/medical content enhancement teams to ensure the end-to-end effective project delivery of the designated publication/medical education deliverables     Qualifications & Experience Experience: 2-4 years post qualification experience Soft skills: Stakeholder management; communication skills; and ability to work independently and within a team environment Technical skills:Project management; Scientific/Medical writing/communications; Pharma experience (including but not limited to therapeutic area/domain knowledge exposure; and/or publication submission) Education: University degree level (Graduate degree, preferably in science).Additionally, relevant advanced/postgraduate degree in life sciences/pharmacy/similar discipline desirable Languages: Excellent knowledge of English language (spoken and written)

Responsibilities Actively partner with Global Science stakeholders to understand their data needs and challenges and, in line with CHC Data & Analytics central standard’s, help them find solution forward to drive improvement. Lead the development and upkeep of advanced AI/ML and analytics data products to advance Science objectives. Offer strategic guidance for evaluating and implementing information management, resource management, and analytics standards for excellence. Lead and participate in industry working groups to contribute to best practices in insights generation, analytics, and reporting. Establish and oversee Data Governance for Science data & analytics Platforms, tools & process to ensure data quality and compliance. Lead a tech-savvy team to adopt new tools and techniques for information storage, access, and analysis, incorporating cutting-edge approaches for Digital Health & Science. Manage the entire lifecycle of AI and Science products, from concept to retirement, as a key decision-maker focused on delivering value to the business and its customers. Conduct customer research and collaborate with key stakeholders to develop and deliver AI and Science data products aligned with business objectives. Ensuring alignment of the product strategy with Digital Architecture guidelines and Data strategy. Leading a team of product team members (both internal & external) and influencing key digital and senior business stakeholders to establish AI/ML/Analytics strategies for the business area. This is accomplished through a disciplined product discovery approach that translates ideas into a prioritized backlog of AI/ML/analytics data product use cases to maximize business outcomes and enhance existing capabilities. Staying informed about external R&D business and technology trends to guide and contribute to ideation and prioritization. Leading and guiding on-shore and off-shore engineers and data analysts to deliver solutions aligned with the Data product roadmap. Enhance the global Advanced Science capability to support project teams for strategic and tactical investment decisions, including digital analytics, mix modelling, and ROI analysis. Oversee the execution and maintenance of top-tier reporting and Science to ensure timely access to the right data for decision-making. Oversee PMO for CHC Digital Health & Science- Ensure accuracy and timeliness of timelines, schedules, cost, and resource models. Support Digital H&S functional leadership and Finance in updating Digital PMO systems promptly.     Qualifications & Experience Proven experience (8+ years) in data analytics, digital strategy, and leading cross-functional teams in an R&D environment. Strong understanding of consumer healthcare products, R&D processes, and regulatory requirements. Proficiency in data analytics tools, statistical software, and data visualization tools. Exceptional problem-solving and critical-thinking skills. Excellent communication and interpersonal skills. Ability to adapt to changing environments and navigate complex challenges. A commitment to maintaining the highest ethical and quality standards in research and development. Strong understanding of healthcare data & technology; cross-industry experience in pharmaceutical, consumer, or technology industry preferred. Strong quantitative and diverse analytical skills: exploratory data analyses, computer science, statistics, modeling, mathematics, programming languages and business acumen Strong communication, negotiation, and interpersonal skills Demonstrated conflict resolution & problem-solving skills in a global environment Strong appetite to learn and discover, entrepreneur mindset Adaptable and open to change Team player, service-oriented Analytical and synthetic, able to formalize solutions, good writing Strong oral and written communication skills With leadership attitude, autonomy and results driven Role model our 4 values: teamwork, integrity, respect, courage Education: Bachelor's, Master's, or Ph.D. in a relevant field (e.g., Data Science, Life Sciences, Pharmaceutical Sciences, or related). Master’s degree preferred.

Responsibilities Develop, review, and evaluate clinical guidelines and Drug Utilization Reviews, provides consultations, develops programs, prepares articles, and conducts research.   Assess the identity, strength and purity of medications. Review prescriptions to assure accuracy, to ascertain the needed ingredients, and to evaluate their suitability. Provide information and advice regarding drug interactions, side effects, dosage and proper medication storage. Analyze prescribing trends to monitor patient compliance and to prevent excessive usage or harmful interactions. Order and purchase pharmaceutical supplies, medical supplies, and drugs, maintaining stock and storing and handling it properly. Maintain records, such as pharmacy files, patient profiles, charge system files, inventories, control records for radioactive nuclei, and registries of poisons, narcotics, and controlled drugs. Advise customers on the selection of medication brands, medical equipment and health-care supplies. Collaborate with other health care professionals to plan, monitor, review, and evaluate the quality and effectiveness of drugs and drug regimens, providing advice on drug applications and characteristics. Compound and dispense medications as prescribed by doctors and dentists, by calculating, weighing, measuring, and mixing ingredients, or oversee these activities. Offer health promotion and prevention activities, for example, training people to use devices such as blood pressure or diabetes monitors. Prepare sterile solutions and infusions for use in surgical procedures, emergency rooms, or patients' homes. Plan, implement, and maintain procedures for mixing, packaging, and labeling pharmaceuticals, according to policy and legal requirements, to ensure quality, security, and proper disposal.     Qualifications & Experience Able to work accurately and with minimal supervision. Ability to comprehend written instructions given by the Doctors and the other related departmental personnel. Ability to plan & organize ones work schedule effectively. Speaking and listening are essential requirements to understand and carry out the instructions given by the supervisors and other related departmental personnel. Affinity to work in team. Enthusiasm. Open-mindedness.