Responsibilities Provides key contributions to clinical strategy, including knowledge and understanding of regional and global regulatory requirements for writing clinical documents including, but not limited to, protocols, clinical study reports, clinical study register summaries, common technical document summaries and Clinical Overview, briefing documents for regulatory authorities, responses to regulatory authority questions, clinical sections of the IMPD for clinical trial applications, investigator brochures and annual reports. Leads matrix teams in planning and production of multiple clinical documents to support regulatory submissions, working with CROs and/or independent contractors as needed. Ensures global approach for submissions as appropriate, including the use of core global modules, supplemented by local modules as necessary. Ideally works in collaboration with GRA to ensure business needs are met for new chemical entities and post approval documentation. Plans and successfully implements large submissions independently or in conjunction with the Medical Writing Director, effectively recommending methods or innovative solutions for achieving accelerated timelines as necessary. Recommends solutions for problems that affect timelines. Provides guidance and facilitation to submission teams in development of detailed submission plan. Ideally demonstrates an understanding of the interdependences of various contributing functions and manages problems affecting timelines as necessary. Ideally demonstrates an ability to quickly assess complex situations, apply scientific, operational and submission development knowledge to identify and implement effective plans for solutions. Proposes resourcing solutions for major projects including number of FTEs required and best use of internal and external resource. Effectively organizes content and arguments in complex clinical submission documents, including briefing documents and responses to regulatory questions. Acts as lead author on submissions. Actively contributes to development of training materials for therapeutic area scientists and provides mentoring and/or training on clinical documentation and submission planning to individuals or teams. Ideally, proactively identifies medical writing training needs for staff and develops/implements training sessions. Has ability to prioritise effectively and meet multiple deadlines successfully with attention to detail, demonstrating high performance standards for own work and encouraging similar standards across the matrix, ensuring standards are proactively applied across a submission.     Qualification & Experience Bachelor’s Degree PhD, PharmD, MPH, MS or other post-graduate degree Possesses highly effective communication skills and is capable of presenting ideas and data clearly to a group, including key stakeholders at senior level. Demonstrated track record of quality decision making and creative problem resolution that impacts program/project direction.  

Responsibilities Responsible for development & design of formulations for multiple products selected for development & conducting meeting with multidisciplinary teams. Conducts relevant patent searches on formulations. Reviews scientific literature & makes recommendations for formulation development strategies. Responsible to carryout Preformulation studies, manufacturing prototype batches & do the formulation development based on QbD approach. Attends appropriate trainings, seminars, & presentations to maintain expertise in formulations & related areas. Communicates with buyers & peers to ensure that APIs, excipients, tooling etc. are available for the project in required quantities, as & when needed. Liaises with the plant operation supervisors & scheduler to ensure that experimental trials / registration batches are planned & executed in a timely manner. Liaises with the documentation groups to ensure that early development trial documents, process evaluation & process optimization documents that are required for execution as required. Coordinates with lab for sample requirement & provides timelines for testing of those samples. Reviews & evaluates data analytical/ technical data on trials, & makes recommendations for bio/stability study batches, & communicates recommendations with management / peers to get necessary clearance to proceed further. Liaises with the documentation groups to ensure that all master manufacturing & packaging documentation, batch documentation, & other related documents required through the duration of the project are made available as & when required. Applies Quality-by-design (QbD) principles to product development & tests the ruggedness of the formula by conducting suitable trials to study the impact of variations in the excipients within SUPAC guidelines / variations in manufacturing process parameters in order to recommend control strategy for CMAs & CPPs. Liaises with the documentation group to ensure that all scale up master manufacturing & packaging documentation & other related documents required for submission to regulatory agencies are made available as & when required. To prepare Pharmaceutical Development Reports & other documents required for regulatory submissions & technology transfer. Responsible for responding to deficiency queries from regulatory agencies in timely manner. Possesses a detailed understanding of the theoretical principles for major manufacturing & a working knowledge of the equipment used in the manufacturing processes & ensures successful execution of experimental trials / registration batches on floor. Responsible for investigating issues with formulations & processes. Uses advanced techniques to identify root cause of issues & plan a course of action for further investigation & corrective action as required. Provides scientific & technical expertise & performs consultations on issues regarding formulation to other members of Formulation Development & other departments. Works as a member of a team to achieve all outcomes. Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, & Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics & Compliance Program, Global Quality policies & procedures, Safety & Environment policies, & HR policies. All other relevant duties as assigned.     Qualification & Experience Master’s degree or Ph.D. in Pharmaceutics or Pharmaceutical Technology or related science. 7-10 years of working experience in a pharmaceutical development environment with related experience in formulation development of solid oral dosage forms for regulated market, scale up and/or technology transfer.  

Qualification & Experience Bachelor's degree in Pharmacy or related field; Licensed Pharmacist with a minimum of 8 years of experience in pharmaceutical procurement, preferably in a manufacturing or production environment. Strong understanding of pharmaceutical regulations, GMP guidelines, and quality assurance principles Excellent negotiation skills and ability to build strong relationships with suppliers/vendors Proficiency in inventory management software and MS Office applications Analytical mindset with the ability to interpret data, conduct market research, and make data-driven decisions Strong organizational skills, attention to detail, and ability to multitask in a fast-paced environment Effective communication and interpersonal skills to collaborate with internal teams and external stakeholders  

  Responsibilities Oversee the operations of our chain of 12 pharmacies Manage the day-to-day activities to ensure smooth operation and profitability Supervise and train pharmacy staff Maintain inventory control and order medications and supplies as needed Ensure compliance with regulatory requirements and company policies Implement customer service standards and ensure excellent customer satisfaction Handle customer complaints and resolve issues in a timely manner Develop and implement marketing strategies to promote the pharmacies Track and analyze sales performance and prepare reports for management Stay up-to-date with industry trends and developments     Qualification & Experience Bachelor's degree in Pharmacy or related field Proven experience as an Outlet Manager or similar role for 7 to 10 years In-depth knowledge of pharmaceutical regulations and guidelines Strong leadership and managerial skills Excellent communication and interpersonal skills Ability to multitask and prioritize Customer-focused with a passion for providing exceptional service  

Responsibilities Develop department wise operating policies which primarily focuses on enhanced patient care and retention of patient for a repeat visit. Planning and reviewing the execution of operational tasks like infrastructure growth, recruiting, performance reviews and compensation, budgeting and accounting. Ensuring seamless flow of information among all key departments/ people for smooth operations. Planning, developing and conducting regular training sessions for all reporting departments in their respective area of work in addition to general training training programs as put forward by the HR department. Participating in staff welfare activities, and staff career planning and growth. Finalization of KRAs of the departmental staff. Coordinating with HR / Quality for the implementation of policies and processes, and for obtaining various quality certifications. Develop innovative / effective strategies to respond to changing economic, social and political conditions Providing details on functional and process challenges and solutions for the same, to the managers, associates & external entities, to guide them towards meeting the desired objectives. Identifying performance targets and accountabilities for the functional units Identifying and addressing deviations and its relevant causes. Highlight, strategic and operational problems and issues in day-t o-day transactions and to work jointly for inclusive solutions

Responsibilities Develop and write high-quality scientific manuscripts, abstracts, and presentations. Ensure all publications are in compliance with industry standards and regulations. Collaborate with research teams to understand study objectives and results. Translate complex scientific data into clear, concise, and engaging content for various audiences. Stay updated on the latest trends and developments in biomedical sciences.     Qualification & Experience Advanced degree (MDS or PhD) in Life Sciences, Biomedical Sciences, or a related field. Certified Medical Publication Professional (CMPP) certification is mandatory. Proven experience in manuscript and publication writing within the biomedical sciences sector with at least two years of experience in industry manuscript writing. Strong understanding of the publication process and ethical guidelines in scientific research. Exceptional writing, editing, and communication skills. Ability to work independently and manage projects with minimal supervision.     Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Roles and Responsiblities Prospect and identify customer cohorts for targeted engagement. Collaborate with cross-functional teams to establish the Obesity Clinic Program, improving managed care settings for obesity across India. Build partnerships and collaborations with healthcare professionals in private, corporate, and aesthetic centers, as well as nutritionists, to enhance obesity care. Lead and implement patient awareness initiatives, such as camps and HCP-PwO interactions, to raise awareness about obesity as a chronic disease.   Qualifications Life Sciences, Science graduate or equivalent. Bachelors/Diploma in Nutrition / Hospital management. Desired Business administration. 5 -8 years of field experience in Launch sales responsibility, Market/therapy shaping pre-launch. Partnership establishment and continued development. Development of Centre of Excellence/On-ground activation.  

Roles and Responsiblities   Developing an understanding of regulations, guidelines, procedures and policies. relating to registration and manufacturing of pharmaceutical products. With management oversight, ensuring data and information packages are fit for purpose. Beginning to understand internal/external CMC Regulatory environment. Begin to build organisational networks. Regular communication with line manager to help identify any CMC issues with business impact. Conducts routine Rx and/or Vx CMC projects with support

Responsibilities Monitoring of IPQA activities Granulation, Compression, Coating, Capsule Filling, soft gel manufacturing, primary and Secondary Packaging Area. Monitoring Exhibit and Validation batches. Preparation and review of process validation and Hold time protocols and reports. Handling of Quality Notifications like Deviations, Change Controls, and its related Documents. Reviews and Approval of CAPA includes tracking, follow-up, reporting/trending and evaluating CAPA and action plan for effectiveness. Review of APQR (Annual Product Quality Review) based on the outcome CAPA shall be initiated. Ensure performance of self-Inspection/ Internal audits (Internal, External, Customer, Visits, and Regulatory) and assist with external quality system audits. Providing response for Manufacturing related regulatory audit observations.   Qualification & Experience 12-15 years in Quality Assurance specifically in IPQA   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Coordinate with PEG Manager to design study analysis plan. Design study analysis plan and Execute feasibility analysis then advice on conduct of full studies. Data and statistical programming/writing code scripts (SQL, SAS/R). Review and approve publication materials for conducted studies. Prepare analyses cohorts based on in-house commercial EMR/claims databases. Develop analyses approaches and procedures in commercial databases for recurrent analyses. Interpretation of output and provides suggestions on improvements. Participate and drive update discussions with the Global PEG team and internal knowledge sharing discussions. Participate in internal team and strategy meetings within NN GBS and HQ. Also, be a buddy for new joiners in the team.   Qualification & Experience Bachelor’s/Masters in Biostatistics, Mathematics, Economics, Engineering, Computer science, Life sciences, Public health or equivalent. Minimum of 7-10 years of experience in data analytics/science, ideally within pharmaceutical industry or consultancy. Minimum 5 years of experience working on patient data and epidemiological studies and statistical analysis. Exposure to product evidence generation strategy and cross functional collaboration. Experience contributing to medical publications preferred.