Responsibilities Provide medical assessment, diagnosis, and treatment to patients presenting in the assigned areas, including emergency cases, critical care patients, and general ward admissions. Monitor patient progress, vital signs, and response to treatment interventions. Administer medications, perform procedures, and coordinate ancillary services as required.     Qualification & Experience Successful completion of MBBS from an accredited medical program Valid medical license from the Medical Council of India Preferred: Experience of 3-5 years in emergency, critical care or wards Excellent communication, interpersonal, and leadership skills Ability to work well in a team environment and handle a high-pressure environment   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Quality Management: Develop and implement quality assurance programs such as NABL, NABH, ISOs and other relevant workplace accreditations in Hospitals. Contribute to cross-functional quality assurance programs such as pharmacy accreditation - Bureau Veritas, HR accreditation - GPTW, etc. Process Improvement: Analyse and make recommendations for improvements that enhance patient safety, satisfaction and outcomes. Collaborate with other department heads and staff to identify inefficiencies in healthcare delivery systems and implement solutions. Risk Management: Identify potential risks to patient safety and health care delivery processes. Develop risk mitigation strategies and protocols - committees and teams. Documentation and Reporting: Maintain accurate data and records of quality assurance activities and outcomes such as committee minutes of meetings, SOP documentation, master control of documents, etc.     Qualification & Experience Bachelor's or Master's degree in healthcare administration, quality management, or related field. Master’s degree preferred. Previous experience in quality assurance or healthcare management preferred. Strong analytical, problem-solving, and communication skills.   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Planning and Forecasting: Analyze usage patterns and forecast demand for medical supplies and equipment to ensure adequate stock levels. Purchasing: Place orders with suppliers, negotiate contracts, and review bids to secure the best pricing and terms. Inventory Monitoring: Regularly monitor inventory levels, track usage, and identify potential shortages or excesses. Supplier Management: Communicate with suppliers to resolve issues, address concerns, and ensure timely delivery of goods. Cost Analysis: Analyze spending patterns, identify cost-saving opportunities, and implement strategies to reduce expenses. Process Improvement: Identify inefficiencies in the supply chain process and implement improvements to streamline operations. Emergency Preparedness: Develop contingency plans and protocols to ensure the hospital is prepared to respond to emergencies or disruptions in the supply chain. Documentation and Reporting: Maintain accurate records of purchases, inventory levels, and supply chain activities, and prepare reports for management review.     Qualifcation & Experience Master’s degree in supply chain management, operations, pharmacy, etc. (MBA preferred) or Bachelor's or Doctor of Pharmacy (Pharm.D.) degree from an accredited institution with proven experience in the relevant fields Preferred: Previous experience in pharmacy management or administration, preferably in a hospital setting. Strong understanding of pharmacy operations, including medication dispensing, compounding, and inventory management.   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities The Critical Care Doctor will be responsible for providing specialized care to critically ill patients in the intensive care unit, monitoring patients, and administering life-saving interventions.     Qualification & Experience Strong clinical background with experience in critical care medicine and emergency medicine Ability to work well in high-stress situations and make quick decisions Excellent communication and interpersonal skills Thorough understanding of medical procedures, equipment, and terminology MBBS or equivalent degree with Critical Care Experience Additional training or experience in specialties like Emergency Medicine   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Use appropriate techniques to diagnose and treat skin ailments. Monitor the effectiveness of skin treatments and make necessary improvements or changes. Communicate with assistants and other team members to ensure therapies are being administered properly. Educate patients on the right ways to achieve healthy, attractive skin. Treat every patient with respect and compassion and ensure compliance with current medical laws and ethics.     Qualification & Experience  MD Dermatology / DNB Dermatology Work Experience: 0-3 yrs   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities The role includes patient care, training and working with physicians to diagnose and treat medical conditions.   Qualification & Experience MBBS Experience working as a Resident Doctor or Medical Officer Expertise in patient care Ability to effectively communicate and collaborate with patients, their families, and physicians Strong problem-solving and decision-making skills   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Serves as a statistical department resource, mentors biostatisticians on job skills, and oversees or develops training plans or materials for Biostatistics associates. Conducts training sessions, or otherwise trains new hires and enhance the skills of existing personnel. Directs the activities of other biostatistics personnel on assigned projects to ensure timely completion of high quality work. Provides independent review of project work produced by other biostatisticians in the department. Provides support across all statistical tasks during the lifecycle of the project, from protocol to CSR. Prepares or oversees the preparation of Statistical Analysis Plans (SAPs), including development of well-presented mock-up displays for tables, listings, and figures. Collaborates with sponsor, if required. May be responsible as Lead Biostatistician for the statistical aspects of the protocol, generation of randomization schedule, and input to the clinical study report. Creates or reviews programming specifications for analysis datasets, tables, listings, and figures. Reviews SAS annotated case report forms (CRFs), database design, and other study documentation to ensure protocol criteria are met and all data is captured as required to support a high quality database and the planned analysis. Implements company objectives, and creates alternative solutions to address business and operational challenges. As biostatistics representative on project teams, interfaces with other departmental project team representatives Preparing in advance for internal meetings, contributing ideas, and demonstrating respect for opinions of others. Conducts and participates in verification and quality control of project deliverables, ensuring that output meets the expected results and is consistent with analysis described in the SAP and specifications. May lead complex or multiple projects (e.g. submissions, integrated analyses), and attend regulatory agency meetings or responds to questions, as needed, to support the statistical analysis results of clinical trials on behalf of the sponsor. Manages scheduling and time constraints across multiple projects, sets goals based on priorities from management, discusses time estimates for completion of study related activities with biostatistics management, adapts to timeline or priority changes by reorganizing daily workload, and proactively communicates to biostatistics management any difficulties with meeting these timelines. Monitors progress on study activities against agreed upon milestones and ensures the study timelines for project deliverables are met. Identifies out of scope tasks and escalates to management. Provides statistical programming support as needed. May participate in Data Safety Monitoring Board (DSMB) and/or Data Monitoring Committee (DMC) activities, including charter development and serving as an independent non-voting biostatistician. May serve as a voting statistician on DSMBs and/or DMCs. Provides input and reviews, and subsequently follows applicable SOPs, WIs, and relevant regulatory guidelines (e.g. ICH). Maintains well organized, complete, and up-to-date project documentation, and verification/quality control documents and programs; ensuring inspection readiness. Displays willingness to work with others and assists with projects and initiatives as necessary to meet the needs of the business. Prepares in advance for internal meetings, contributes ideas, and demonstrates respect for opinions of others Supports business development activities by contributing to proposals, budgets, and attending sponsor bid defense meetings. Performs other work-related duties as assigned. Minimal travel may be required.     Qualification & Experience Graduate degree in biostatistics or related discipline. Min 8 years experience in clinical trials or an equivalent combination of education and experience, demonstrated by the ability to lead multiple projects and programs of studies.  

Responsibilities The RA Executive shall report to the Head of QA/RA, and is responsible to assist him in the following areas: Leading new products registration and license renewal in various countries Compliance for international as well as local regulations for various class of medical devices To Lead QA/RA team and ensure quality SOPs within the company Have the joint responsibility to develop, facilitate and execute comprehensive regulatory strategies through all phases of development and product life cycle, to accelerate and ensure successful product registrations and provides regulatory assessment and supports Change Control Assessment Oversee maintenance of product quality and compliance through the Quality Assurance functions as well as management of the Quality Management System and compliance processes Remains knowledgeable about current regulations and guidance, interprets and implements in the assigned projects Keep abreast of International legislation and guidelines of current product line in India Compliance with respect to internal/external audits meeting regulatory/ accreditation requirements Reviewing current accreditation/regulatory requirement, performing gap analysis and ensuring compliance to current requirements Provide product specific Regulatory strategies to mitigate risk; works in conjunction with production, RA & QA team to provide advice on process and labeling changes Review of SOPs, BPRs, specifications and change control to ensure compliance 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 the management team Responsible for ensuring compliance to the submission standards, procedures and policies in India Support Commercial Department in business development such as product evaluation and pre-launch activities Support Marketing/sales department for product review, product function training, catalogue preparation, content management, field queries resolution etc     Qualification & Experience More than 2 years of experience in technical documentation, regulatory affairs and quality assurance in the medical device industry Bachelors degree in relevant field. Master's is desirable Ethical behavior and high level of integrity    

Responsibilities Responsible for QMS management for Change Control / Deviation / Investigation / CAPA / OOS / OOT, APQR etc. Preparation, review & approval of SOP’s, Site Mater file, VMP etc. Response preparation for the External audit (Customer or Regulatory or third parties.). Preparation, scheduling & conducting self – inspection audits. Responsible for handling Market Complaints & conducts Investigations for timely response to customer. To ensure annual product review is completed as per the timeline and review the control samples of finished product and report prepared. Review and Issuance of WOP to Production, Insurance of control documents to other departments. Quality Parameter checks for Retain samples/ APQR samples and documentation.     Qualification & Experience M.Sc / B. Pharma with minimum 8 to 10 years of relevant experience in Quality department in Pharma Industry (Formulation plant). Well verse with GMP, GDP, Change control, deviation, QMS.   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Manages and provides leadership to an efficient and effective regulatory affairs team. Assists in the career growth of Associates and Senior Associates. Plans and manages regulatory submissions and activities for products throughout the life-cycle of a product in compliance with Health Canada regulatory requirements and ICH guidelines. Reviews submissions, including deficiency letters, to ensure timeliness, accuracy, consistency, completeness, and compliance with regulatory standards. Ensures that technical data and regulatory summaries are presented clearly and succinctly to optimize the regulatory authority review and approval process. Provides support to junior staff in the creation of submission documents and coach as necessary to ensure continuing development of regulatory skills. Ensures regulatory maintenance of approved drug products. Helps regulatory staff overcome difficulties in the completion of projects by diplomatically managing relationships with business partners, regulatory agencies and internal staff. Provides strategic guidance and advice. Contributes to the creation of submission strategies throughout the product life cycle. Shows good judgment to determine when to escalate problems to the Director of Regulatory Affairs. Tracks critical attributes of projects to ensure accountability and efficiency. Creates or supports the generation of reports as required. Supports the Director in developing and implementing departmental goals to coincide with corporate goals. Contributes to the creation and implementation of standards and best practices within the department to improve efficiency and quality of processes. Reviews internal documentation (labeling, master batch records, specifications) and external documentation (clinical reports) for adherence to regulatory guidelines. Builds and maintains a healthy working relationship with business partners. Liaises with partners to collect documents and information for submission preparation or in response to technical queries/deficiency letters. Builds and maintains a good working relationship with regulatory agencies. Uses the relationship to understand expectations beyond that which is presented in guidelines and policy statements. Maintains current awareness of regulatory guidelines (Health Canada, ICH, FDA, etc.). Provides sound regulatory input and support to product development and technical transfer projects. Represent Regulatory Affairs on interdepartmental teams for projects with Operations, Development, QA, Marketing, and other functions as required. Provides cross-functional review/input from a regulatory, scientific and technical viewpoint. Maintains and applies knowledge of product data, marketing objectives, and quality procedures. May perform other regulatory affairs functions and activities as required to achieve departmental or operational priorities and prioritizes other responsibilities to meet additional work requirements.     Qualification & Experience University degree in Science, Pharmacy, Life Sciences with post-graduate certification in Regulatory Affairs program. No less than 8 years of relevant industry experience No less than 3 years of relevant Health Canada and sterile injectable experience   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"