Qualification & Experience MHA With 4 years’ experience in Quality Department can apply   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Ensure full compliance with governance principles while seeking appropriate business solutions Lead and perform as the Local Operating Company (LOC) medical signatory related to promotional and non-promotional material requiring copy approval for selected markets Work with the Commercial Content Specialist to ensure that materials going to market are in line with the GSK strategy and to the required standard. Confirm translation accuracy of all materials Support Medical Material content monitoring and Corrective and Preventive Actions (CAPA) Tracking     Qualifications & Experience PharmD – Pharmacist degree or PhD in life sciences Experience in copy approval and governance Experience with content that involves basic sciences Experience with content for disease areas such as infectious disease, respiratory, vaccine, preventable illness Doctor of Medicine degree (MD) Excellent verbal and written communication skills Demonstrated learning agility with an ability to problem solve Demonstrate a high level of personal accountability and integrity

Responsibilities Collaborate with Clinical stakeholders to understand their business needs and challenges, design and architect AI solutions ensuring scalability, reliability, and performance. Build knowledge on business priorities/strategic goals and leverage this knowledge while building requirements and solutions for each business need. Demonstrate deep knowledge and expertise in foundational and large language models, as well as related AI technologies and frameworks. Identify potential challenges, constraints, and opportunities for innovation in Clinical space to provide recommendations and propose effective solutions. Develop POCs to validate and showcase the feasibility and effectiveness of the proposed AI solutions. Define best AI/ML driven practices and AI lifecycle Work across functions to develop and architect AI solutions using NLU, ML, and AI. Design, build, and deploy predictive models and statistical analyses to solve business problems and optimize processes. Conduct thorough testing and validation of models to ensure accuracy, reliability, and scalability. Accelerate the delivery of AI use cases in collaboration with the other AI teams to deliver the highest business impact use cases. Develop, improve, and carry out plans for using AI and its effects, along with finding new ideas and partnerships to help. Choose the right AI tools and models for the job and build and train them using Python and other free technologies. Collaborate with different teams to create AI solutions that can generate new content using language understanding and machine learning. Provide technical guidance and mentorship to junior team members, and actively participate in knowledge sharing activities.     Qualifications & Experience Bachelor's degree in a relevant scientific discipline (e.g., Biomedical engineering, Life Sciences, Nursing, Pharmacy, clinical background (e.g., MD - Doctor of Medicine OR RN - Registered Nurse) Advanced degree (e.g., Master's or Ph.D.) in Data Science, AI/ML Overall experience of 7-9 years with minimum of 3-5 years of experience in clinical research, with a focus on managing clinical trials in a pharmaceutical, biotechnology, or contract research organization (CRO) setting. Minimum of 3-5 years of experience in AI research and development, with a focus on healthcare or life sciences applications Strong understanding of clinical trial regulations and guidelines, including Good Clinical Practice (GCP), International Conference on Harmonization (ICH), and applicable local regulations. Proven experience in designing and delivering AI solutions, with a focus on foundation models, large language models, or similar technologies. Experience in natural language processing (NLP) and text analytics is highly desirable. Ability to understand customer needs and business objectives in Pharmaceutical domain preferably Clinical. Experience in working closely with clinical Statisticians/Study Builder/ Study Designers and translating their requirements into effective AI solutions. Strong programming skills, with proficiency in Python, R and experience with AI frameworks such as TensorFlow, PyTorch, or Hugging Face. Understanding in the usage of libraries such as SciKit Learn, Pandas, Matplotlib, etc. Familiarity with cloud platforms (e.g., AWS, Azure, GCP) and related services is a plus. Experience working with large datasets and performing data pre-processing, feature engineering, and model evaluation. Experience in solution architecture and design, translating business requirements into technical specifications, and developing scalable and robust AI solutions. Excellent interpersonal and communication skills. Engage with stakeholders for analysis and implementation. Commitment to continuous learning and staying updated with advancements in the field of AI. Demonstrate a growth mindset to understand business processes and challenges

Responsibilities Coordinates and maintains Labelling lists for Teva products Collaborates with relevant PV departments (Medical Scientific unit, Data Management groups and IT) Provides responses and guidance for other PV and non-PV Teva employees Maintains relevant Labelling list operating procedures Participates in meetings and discussions relevant for Labelling list coordination Collaborates with other departments on relevant system upgrades and process optimization projects involving labelling lists Assures all tasks are performed in line with relevant procedures Other tasks as assigned by the direct manager     Qualification & Experience University degree (Preferably in health care domain) 2-3 years of Health care or Pharmaceutical industry experience and at least 1 year of Pharmacovigilance experience  

Responsibilities Conducting Research: Assist in designing and executing research studies and experiments to investigate healthcare-related questions and hypotheses. Data Collection: Collect and organize data from various sources, including literature reviews, surveys, interviews, and experiments, ensuring accuracy and completeness. Data Analysis: Analyze research data using statistical methods and software tools, such as SPSS, R, or Python, to identify patterns, trends, and correlations. Interpretation of Results: Interpret research findings and draw meaningful conclusions to inform decision-making and guide future research directions. Literature Review: Conduct comprehensive literature reviews to stay abreast of the latest developments and findings in healthcare research and related fields. Documentation and Reporting: Prepare research reports, presentations, and scientific publications summarizing study objectives, methods, results, and conclusions. Collaboration: Collaborate with cross-functional teams, including scientists, engineers, clinicians, and product developers, to integrate research findings into product development and innovation processes. Quality Assurance: Ensure compliance with research protocols, ethical guidelines, and regulatory requirements throughout the research process. Willing to travel within Bangalore and other onsite clinical research location in India   Qualification & Experience Master's or PhD degree in a relevant field, such as Biomedical Engineering, Health Sciences, Public Health, or a related discipline. Strong academic background with coursework or research experience in healthcare, biomedical research, or a related field. Proficiency in research methods and data analysis techniques, with experience using statistical software tools such as SPSS, R, or Python. Excellent analytical and critical thinking skills, with the ability to interpret complex data and draw meaningful conclusions.  

Responsibilities **Market Analysis:** Conduct thorough market research and analysis to identify trends, opportunities, and potential areas for expansion within the healthcare industry. **Strategic Planning:** Develop and execute strategic business development plans to drive growth, increase market share, and achieve revenue targets. **Client Relationship Management:** Build and maintain strong relationships with key clients, healthcare providers, insurers, and other stakeholders to drive collaboration and foster long-term partnerships. **New Business Development:** Identify and pursue new business opportunities, including client acquisitions, partnerships, and strategic alliances, to expand Wundrsight Healthcare's reach and impact. **Sales and Negotiation:** Lead the sales process from prospecting to contract negotiation and closure, ensuring alignment with company objectives and delivering value to clients. **Cross-Functional Collaboration:** Work closely with internal teams, including marketing, product development, and operations, to align business development strategies with overall company goals and objectives. **Performance Tracking and Reporting:** Monitor and analyze key performance metrics, such as sales pipelines, conversion rates, and revenue forecasts, to assess the effectiveness of business development initiatives and inform future strategies.   Qualification &  Experience MBA, Master's degree in Business Administration, Psychology, Marketing, Healthcare Management, or related field. Min. 2-3 years of experience in business development, sales, or a related role within the healthcare industry. Proven track record of achieving or exceeding sales targets and driving revenue growth. Strong understanding of the healthcare landscape, including industry trends, regulatory environment, and key players. Excellent communication, negotiation, and interpersonal skills. Strategic thinker with the ability to develop and execute plans to achieve business objectives. Highly organized, with the ability to prioritize and manage multiple projects simultaneously. Team player with the ability to collaborate effectively across departments and levels of the organization. Prior experience in the mental health, healthtech or medical device industry is a PLUS    

Responsibilities Assessment of change controls for registration impact and implementation of all necessary dossier changes in; Europe and International Market Responsible for compilation of the variations for the products in the product portfolio in collaboration with other stakeholders Compiling variation packages Experienced in managing, regulatory database and Trackwise.     Qualification & Experience Academic degree- and thinking level with a chemical/pharmaceutical background. 2-5 years of experience in CMC Regulatory Affairs; Mainly in Europe and International Market Knowledge on registration procedures and pharmaceutical regulations Interest and capability to work with different software, including Document Management System  

Responsibilities Develop and execute the R&D and Quality strategy aligned with the overall business objectives. Led cross-functional teams to drive innovation, product development, and process improvements. Provide guidance and direction to R&D and Quality teams, fostering a culture of continuous improvement and excellence. Lead R&D initiatives to develop new food products, formulations, and recipes that meet consumer preferences, market trends, and regulatory requirements. Collaborate with internal stakeholders, including marketing, operations, and sales, to identify market opportunities and translate consumer insights into innovative products. Manage product development projects from concept to commercialization, ensuring alignment with timelines, budgets, and quality standards. Establish and maintain robust quality management systems and procedures to ensure compliance with food safety regulations (e.g., FDA, HACCP, GMP). Implement quality control measures throughout the manufacturing process, from raw material sourcing to finished product distribution. Conduct regular audits, inspections, and testing to monitor product quality, identify non-conformances, and implement corrective actions. Stay abreast of food safety regulations, industry standards, and best practices to ensure compliance with relevant requirements. Recruit, develop, and mentor a high-performing team of R&D and Quality professionals, including food scientists, technicians, and quality assurance specialists. Conduct training programs and workshops to enhance employee skills and knowledge in food science, quality management, and regulatory compliance. Collaborate with internal stakeholders, including senior management, production, procurement, and supply chain, to ensure alignment of R&D and Quality initiatives with business goals. Engage with external stakeholders, including suppliers, customers, and regulatory agencies, to build strategic relationships and address quality-related issues. Represent the company at industry conferences, seminars, and trade shows to showcase R&D innovations and quality assurance practices.     Qualification & Experience Masters/Bachelor's or advanced degree in food science, food engineering, Dairy or a related field.. Extensive experience (typically 12+ years) in R&D and quality management roles within the food manufacturing industry. Strong knowledge of food safety regulations, quality management systems, and industry standards (e.g., FSMA, SQF, BRC). Proven track record of driving innovation in food product development, formulation, and commercialization. Experience managing cross-functional teams and leading projects from concept to commercialization.  

Responsibilities Continue to uplift and bridge service gaps in the existing COE to create a consolidated hub for Frontline excellence. Improvements and drive analytical and consulting in designing and execution of projects. Good commercial knowledge from Pharma industry to add value to the business discussions and decisions. Experience in managing a diverse team across Front line domains by hiring the right talent and develop the internal talent as well to further collaborate with business. Ensure superior customer satisfaction by delivering high end quality support along with team. Supporting strategic recommendations to key business questions, based on research results. Collaborate and ensure strong engagement within CA management team to achieve a common department goal. Driving vendor support and contracts for specific time bound needs.   Qualification & Experience MBA, Graduation in Pharmacy, life science/Engineering background. 10+ years of experience in incentive compensation planning, field force effectiveness, and front-line excellence/consulting. Strong analytical capabilities, with demonstrated experience in analyzing complex situations and driving strategic projects and initiatives. Good commercial knowledge of the pharmaceutical industry.  

Responsibilities Collaborate with cross-functional teams to develop and refine clinical trial strategies, ensuring alignment with scientific objectives and business goals. Provide scientific leadership and guidance throughout the lifecycle of clinical trials, including protocol development, study design, and scientific review of study-related documents. Contribute scientific insights to the selection of investigational sites, study endpoints, and the evaluation of scientific data, supporting the development of clinical trial protocols. Identify potential scientific and operational risks within clinical trials and develop proactive strategies to mitigate these risks, ensuring the scientific integrity of the studies. Stay abreast of relevant regulations, guidelines, and industry best practices, providing scientific input to ensure compliance with regulatory requirements in clinical trial conduct. Collaborate with cross-functional teams to interpret scientific data, ensuring accurate and meaningful presentation of clinical trial results. Coordinate early trial feasibility input. Organize recurrent insights sharing within and from the clinical medical manager (CMM) network. Identify early TA trends and plan solicited insights among CMMs. Identify common trial challenges and suggest CMM intervention points.   Qualification & Experience Should possess Bachelor’s/Advanced degree in a scientific discipline (e.g., MD, PhD, PharmD, MDS). Should possess at least 2+ years of clinical and/or pharmaceutical industry experience. A strong understanding of clinical research and drug development processes. Demonstrated research experience (e.g. publications). Proven experience in clinical operations, clinical trial management, or related roles within the pharmaceutical, biotechnology, or clinical research industry. Strong understanding of regulatory requirements and guidelines governing clinical research.