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Title: Sr. Manager-Regulatory Medical Writing Date: Jul 14, 2025 Location: Gurgaon - R&D Company: Sun Pharmaceutical Industries Ltd Job Purpose Clinical Development department is one of the key departments at SPIL which handles, analyzes, and portrays scientific data and information. Providing authentic, objective, and accurate information to regulatory agencies, the scientific community, healthcare professionals, and patients in a consistent and timely fashion across the entire drug development cycle is fundamental to SPIL. The purpose of SPIL Medical Writer is to work with cross-functional, multidisciplinary teams to author, manage, and lead the development of documents intended for regulatory agencies and audiences (including but not limited to Protocols, Clinical Study Reports, Investigator Brochures, Briefing Documents, Submission Documents, Health Authority Regulatory responses, IND/NDA Applications and Marketing Authorization Applications). Key Roles and Responsibilities Preparation of the medical writing documents under the purview of Clinical Development department that may be required for domestic and international regulatory submissions across the globe. Effectively collect, and evaluate data, information, and inputs from multiple functions, sources to create a cohesive content strategy for writing projects Plan including organizing/preparing outlines, write, edit, review, co-ordinate, obtain approval, and complete the regulatory documents supporting Clinical Development Conduct effective document initiation meetings and comments resolution meeting(s) to ensure review team alignment and understanding Ensure data are presented in a clear, complete, accurate, and concise manner. Ensure key data, statements, and conclusions are consistent across related documents and that inferences/conclusions are integrated, accurate, and supported by appropriate data. Coordinate scientific reviews, collate reviewer’s comments, develop content of document as required based on internal/external inputs, and prepare final version. Ensure and coordinate quality checks for accuracy; perform quality checks of documents Perform peer review of documents Exhibit flexibility in working across multiple document types and therapeutic areas Influence or negotiate content of document and timelines, with cross functional teams to deliver optimum quality documents Escalate issues if any, to medical writing supervisors/HOD Anticipate and mitigate risks to delivery Maintain and enhance TA knowledge of SPIL portfolio Maintain and be abreast of medical writing regulatory guidelines / policies/ procedures Maintain and enhance scientific knowledge skills to align with audience needs and changes in technology and platforms Provide coaching to others by sharing technical information and providing guidance Maintain/ support metrics, tracking sheets, and training records as per the process requirements Complete required trainings within stipulated due dates Be audit compliant and audit ready per organizational needs Network with others (medical writing team and other functions) to identify and share best practices. Contribute to process improvements May build and manage relationships with vendors, if required. Qualification, Skill and Competencies Requirements Qualification: A doctoral or post-graduate degree in Life Science/Pharmacy disciplines or clinical degrees (MBBS/BDS/BAMS/BHMS, etc.) with minimum of 3 years of experience and good knowledge in regulatory medical writing, with proven and progressive leadership capabilities is required. Advanced degree (e.g., MD, PhD) is preferred… Skills and Competencies Good knowledge of scientific, statistical, and research principles and regulatory guidelines such as ICH requirements. Demonstrated written and/or communication skills. Demonstrated project management and decision-making skills. Demonstrated interpersonal skills to build relationships, act as change agent, and adapt to rapidly changing organizational & business challenges. Demonstrated innovative thinking to allow for optimal execution of clinical development strategies. Good knowledge of global regulations and pharma industry standards Job Duration Full Time Part time Job Location Mumbai/ Gurgaon, INDIA Reporting To Global Medical Writing Lead/ Head - Global Medical Writing

NEED A 24\*7 RESIDENT DOCTOR (MBBS/MD) WHICH HAS GOOD PRACTICE FOR OUR WELL EQUIPED HEXO HOSPITAL.WE WILL PROVIDE MEELS & ROOM FOR STAY. ALSO PROVIDE MOBILE EXP + ALL DAY WiFi etc. Job Type: Full-time Pay: ₹850,000.00 - ₹1,400,000.00 per year Benefits: Cell phone reimbursement Food provided Schedule: Fixed shift Supplemental Pay: Performance bonus Work Location: In person

Qualification: MBBS Medical degree (MBBS or equivalent) Valid medical license to practice in the region Completed residency in a relevant medical field Previous experience in a hospital or clinical setting, preferably in emergency or night shifts Strong decision-making and problem-solving skills Excellent communication and interpersonal skills Ability to work independently and under pressure Skills Patient assessment Emergency response Treatment planning Medical documentation Medication prescribing Critical thinking Team coordination Communication Job Type: Full-time Schedule: Night shift Work Location: In person

Roles & Responsibilities \* Engage with potential customers via phone calls, providing information about NEET-PG/FMGE courses. \* Convert leads into sales and ensure smooth handover to the post-sales team. \* Manage and update customer information in our CRM or sales software. \* Collaborate with the sales manager for daily reporting and performance tracking. \* Assist in developing and executing strategies for user acquisition and sales growth. Qualifications: Requirements and skills- \* 1-2 years of experience in abroad counselling, preferably in MBBS , NEET courses \* Strong communication and interpersonal skills. \* Proficiency in CRM management or similar sales software. \* Ability to work independently and as part of a team. \* A proactive approach to problem-solving and customer engagement Thanks & Regards HR Team Job Type: Full-time Pay: ₹20,000.00 - ₹28,000.00 per month Benefits: Cell phone reimbursement Work Location: In person

Role and Responsibilities ● To provide in-person clinical consultation and teleconsultation at a primary health centre based in Sahakar Nagar, Bangalore. ● Carry out the diagnosis, treatment based on standard management protocols and guidelines, counselling and also referral, where and when necessary. ● Evaluate patients and provide appropriate medical treatment for various illnesses and injuries. ● Explain procedures or prescribed treatments to patients. ● Maintain confidentiality and impartiality at all times. ● Collect record and maintain sensitive patient information such as examination results, medical history and reports. ● Keep up-to-date with medical developments, treatment and medication. ● Document all patient evaluations, treatments, medications and transactions according to company policies and procedures ● Besides physical consultation , communicate with patients through Online mode (i.e. e-consultations on voice/video/chat) ● Help in organizing Health Camps at community and corporate level whenever required. Job Types: Full-time, Permanent Pay: ₹60,000.00 - ₹80,000.00 per month Benefits: Health insurance Leave encashment Paid sick time Provident Fund Application Question(s): Is your MBBS from India? Are you planning NEET this year? Or are you planning PLAB/USMLE? How many years of experience you have post internship? Do you speak Kannada? The shift timings are from 9.30 am to 1 pm and 4 pm to 8.30 pm. You are required to do both the shifts. Are you OK with the shifts? Are you staying close to Sahakar Nagar.( within 5-6 km) or willing to relocate to Sahakar Nagar? Work Location: In person

JD - Teleconsultation Role Job Title: Teleconsultation Doctor – Prescription Validation Job Type: Full time/Part-Time Working Hours: 3:00 PM to 1:00 AM Shift Duration: 5 hours (Part time) - Break : 25minutes 9 hours (Full time) - Break : 50 minutes Job Role: As a Teleconsultation Doctor at MyRx, you will be responsible for prescription validation and conducting proper teleconsultations to ensure accurate and safe medical guidance for patients. Key Responsibilities: Prescription Validation. Review prescriptions received as orders. Accept the order and initiate a call through the system. Verify prescribed medicines with the patient. Approve the order after validation. Requirements: MBBS & MBBS Valid and registered medical license in India. Prior experience in teleconsultation (preferred). Strong communication and patient-handling skills. Job Types: Full-time, Part-time Pay: ₹20,000.00 - ₹40,000.00 per month Expected hours: 35 – 63 per week Benefits: Work from home Schedule: Day shift Evening shift Fixed shift Morning shift Rotational shift Weekend availability Supplemental Pay: Overtime pay Performance bonus Application Question(s): Do you have Medical council license? Experience: Teleconsultation: 1 year (Preferred) Work Location: Remote Application Deadline: 20/07/2025 Expected Start Date: 16/07/2025

Mukat Hospital is seeking experienced ICU nursing staff to join our dedicated healthcare team. Key Responsibilities: Monitor and manage critically ill patients admitted in the ICU under the guidance of the ICU In-Charge or Intensivist. Perform daily clinical rounds, assess patient condition, and implement treatment plans as per protocols. Respond promptly to medical emergencies in the ICU, initiate resuscitation procedures (CPR, intubation, defibrillation). Monitor vital signs, ventilator settings, invasive lines (CVP, arterial lines), and ensure proper patient care documentation. Administer prescribed medications, infusions, and manage blood products as per standard ICU protocols. Maintain clear communication with senior consultants, nursing staff, and patient attendants regarding patient progress. Ensure proper handover of critical information during shift changes. Follow infection control protocols and ICU care bundles. Assist in ICU procedures such as central line insertion, arterial cannulation, intubation, tracheostomy, etc., under supervision if required. Attend Code Blue situations within the hospital premises when on duty. Maintain updated patient records and ICU charts as per hospital norms. Qualification & Experience: MBBS/BAMS degree with valid registration from Medical Council. Preferably with ICU experience (minimum 1 year) or Critical Care certification. BLS/ACLS certification preferred. Job Type: Full-time Work Location: In person

Position: IVF Consultant/Specialty (Female) Job Description: Full time and permanent job Only Female candidates can apply Job Location, SRINAGAR Requirement: MBBS Any post graduate (MBBS, DGO) Handle OPD and Campaign Activity. Minimum 1-3 yrs experience. Please share your resume at [email protected] Job Types: Full-time, Permanent Pay: ₹900,000.00 - ₹2,000,000.00 per year Experience: total work: 2 years (Preferred) Work Location: In person

Summary To write, support and manage projects to prepare high quality medical and scientific communications including, literature review, abstracts, posters, slide sets, Manuscripts (complex) for publication/ presentation at congresses or internal medical and/or clinical team. About the Role Location – Hyderabad #LI Hybrid Major Responsibilities: Prepares, literature review, abstracts, posters, and slide sets, and Manuscripts (complex) working from various data sources including clinical study reports, patient profiles, protocols etc. Performs quality control (QC) checking / proof reading of the above-mentioned deliverables to meet customer expectations. Manages multiple projects of up to two brands at any given time. Obtains feedback from customers and implements customer management tactics. Complies with and support group’s project management tool, standards, policies and initiatives. Follows Novartis specifications for documentation, specifically Novstyle, templates etc. Follows and tracks clinical trial milestones for assigned projects. Maintains records for all assigned projects including archiving. Maintains audit, SOP and training compliance. Train new joiners, fellow colleagues as and when required. Performs additional tasks as assigned. Minimum Requirements: Minimum Education - Science degree or equivalent, B.Sc./equivalent with 8 years Clinical Research (CR) experience, M.Sc./M.Pharm +6 years of clinical research (CR) experience. Desired – Doctoral Degree or Qualification in Medical Sciences (MBBS/MD/equivalent). PhD + 4 year of CR experience, MBBS/equivalent + 4 year of CR experience, MD +2 years of CR experience. Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division US Business Unit Universal Hierarchy Node Location India Site Hyderabad (Office) Company / Legal Entity IN10 (FCRS = IN010) Novartis Healthcare Private Limited Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job Title: Consultant Oral Maxillofacial Surgeon Location: Greater Kailash II (M-Block Market), New Delhi Employment Type: Full-Time About The Face Company The Face Company is a luxury aesthetic destination where clinical precision meets artistic excellence. Grounded in scientific innovation and advanced technology, we offer bespoke semi-permanent makeup, cutting-edge facials, and holistic wellness solutions designed to enhance and refine natural beauty. Our commitment to transformative, results-driven care underpins everything we do, creating an elevated experience for a discerning clientele. Key Responsibilities Client Consultations & Treatment Planning – Conduct comprehensive skin assessments and medical history reviews – Develop bespoke treatment plans integrating medical and aesthetic modalities – Manage follow-up consultations to monitor progress and adjust protocols Advanced Aesthetic Procedures – Perform medical facials (e.g., ZO Red Carpet Peel, Hydralogica), microneedling, laser hair reduction, RF-based eye treatments, and injectable therapies (e.g., Skinvive) – Supervise semi-permanent makeup protocols to ensure safety and efficacy – Oversee scalp micro-pigmentation and enzyme-based hair regrowth treatments Clinical Leadership & Training – Mentor and train skin therapists and nurses in protocol adherence and best practices – Ensure strict compliance with hygiene, sterilization, and safety standards – Introduce new technologies and techniques to keep the center at the forefront of innovation Brand Representation & Collaboration – Participate in client-facing events, educational workshops, and PR initiatives – Collaborate with the marketing team on content, campaigns, and ambassador programs – Maintain accurate documentation and contribute to continuous improvement projects Qualifications MBBS with MD/DNB in Dermatology (or equivalent recognized qualification) MDS Oral Maxillofaical Surgeon Valid medical license to practice in India Minimum 3–5 years’ experience in aesthetic and clinical dermatology Certified training in lasers, injectables, and energy-based devices Strong clinical judgment, attention to detail, and commitment to patient safety Excellent interpersonal skills and ability to deliver concierge-level service Passion for staying abreast of industry trends and new treatment modalities What We Offer Competitive salary with performance-based incentives Ongoing professional development and international training opportunities State-of-the-art facility equipped with the latest aesthetic technologies A supportive, collaborative environment within a luxury-driven brand Job Types: Full-time, Permanent Pay: ₹80,000.00 - ₹110,000.00 per month Ability to commute/relocate: Greater Kailash, Delhi, Delhi: Reliably commute or planning to relocate before starting work (Required) Work Location: In person