1075 Pharmacology Jobs - Page 20

In this role you will be responsible for: The coder reads the documentation to understand the patients diagnoses assigned - Transforming of healthcare diagnosis, procedures, medical services, and equipment into universal medical alphanumeric codes - Creating uniform vocabulary for describing the causes of injury, illness & death is the role of medical coders - Medical coding allows for Uniform documentation between medical facilities - The main task of a medical coders is to review clinical statements and assign standard codes Requirements of the role include: - 0 -1 Year of experience in any Healthcare BPO - University degree or equivalent that required 3+ years of formal studies in Life science/BPT/Pharm/Nursing - Good knowledge in human Anatomy/Physiology - 1+ year(s) of experience using a computer with Windows PC applications that required you to use a keyboard, navigate screens, and learn new software tools - Ability to work scheduled shifts from Monday-Friday 7:30 AM to 5:30 PM IST and the shift timings can be changed as per client requirements. - Flexibility to accommodate overtime and work on weekend s basis business requirement. - Ability to communicate (oral/written) effectively in English to exchange information with our client. Must be a CPC-A Certified and working from office mandatory

MD Medicine required at Gohana Haryana Salary 3.5 to 4 Lakhs + Accommodation Rewari Haryana Salary 3.5 to 4 Lakhs + Accommodation Ambedkar Nagar UP Salary 3.5 Lakhs + Jhajjar Haryana Salary 3.5 Lakhs + Accommodation Required Candidate profile Azamgarh UP Salary 3.5 Lakhs + Share + Accommodation Sonipat Haryana With Critical Care Fellowship Salary 3.5 Lakhs + Accommodation Varanasi UP Salary 2.5 to 3 Lakhs Kanpur UP Salary 2.5 Lakhs

Primary Job Function With minimal Manager Support:- 1. Product registrations /Submissions Leads and coordinates project registrations for complex filings, including new product introductions Identifies and collects data needed, or delegates where appropriate Seeks and evaluates expert advice and technical support where necessary Prepares responses to deficiency letters 2. Relationships & Cross Functional team work Represents Regulatory Affairs at relevant meetings and presents agreed RA position Provides expert advice and technical support to cross-functional colleagues Monitors actual versus planned activities and timelines. Proactively identifies and communicates risks and issues impacting project progression. 3. Affiliate Coordination Maintains strong working relationships with Regional Product leads and Affiliate colleagues 4. Compliance across Life-Cycle Assesses and approves change requests and ensures files are updated accordingly Has expert knowledge of legislation and current developments within specific area of business Acts as a subject matter expert within specific area of business Manages corrective action plans and drives to completion within agreed timelines 5. Strategy Leads and coordinates the development of regulatory product strategies for assigned products and projects Identifies, communicates and mitigates regulatory risks 6. Process Improvement Independently identifies opportunities and suggests improvements for resolution Leads the development of position papers & work aids etc 7. Health Agency Interaction Takes a leading role in preparing for and attending Health Agency meetings as appropriate Liaises (including acting as the single point of contact if necessary) with Notified Bodies and other medical device organisations (may not be applicable to all staff) 8. Licensing Reviews Leads and coordinates regulatory due diligence activities for assigned projects 9. Technical competency Has expert knowledge of global regulatory requirements Has specialist regulatory knowledge of assigned country, region, product class requirements Has expert knowledge of allocated products Takes active steps to keep knowledge current CORE COMPETENCIES Anticipation Develops scenario and contingency plans that ensure achievement for results under changing conditions and situations Takes initiative to implement change to mitigate risks, solve issues or improve processes and ways of working. Actively gathers customer inputs in order to anticipate and fulfill their needs and requirements Manages internal/external stakeholders to identify and address issues Understands the situation or audience and adjusts approach to achieve desired outcomes Adaptability Effectively prioritizes and plans long-term (months/years) work tasks and projects Develops “big picture” thinking to Identify synergies and opportunities across the organisation Regularly reviews commitments and re-prioritises activities or negotiates timelines as necessary Reacts quickly to solve problems and issues as they arise Provides guidance and advice to colleagues Initiative Has a clear understanding of the organisation and the roles of other functions Proactively anticipates, mitigates and avoids problems and issues Proactively seeks feedback from manager and team members and adapts behaviour to improve performance Maintains strong customer focus. Innovation Uses intrapreneurial skills to identify and execute new or unique ways to address work problems and opportunities Creates an environment of experimentation and uses failure as an opportunity to learn and take alternate action Challenges current thinking and generates new ideas. Encourages others to do the same Integrates information from multiple sources to generate unique insights or new solutions that increase competitiveness Leverages diversity of people and thinking to create a competitive advantage Collaborates across boundaries to create cross-business opportunities Integrity Delivers high quality results Meets agreed deadlines Exhibits honesty and presents complete impartial information Displays consistency between words and actions Acknowledges and responds constructively to failures and mistakes Expresses dissatisfaction constructively, without over-reacting Teamwork Actively drives completion of individual and shared goals LEADERSHIP COMPETENCIES Set Vision and Strategy Uses influencing and negotiation skills to drive strategic alignment of key cross-functional stakeholders Drives the generation of robust regulatory strategies for complex global projects Build Organization and Inspire People Mentors junior team members Provides training and support on areas of subject matter expertise Demonstrates leadership skills in day to day work and encourages the same traits in others Provides insight, knowledge and leadership to improve functional area and build the business Develops and demonstrates strong leadership skills and encourages others to do the same Drive Results Displays energy and persistence to drive the organization forward Delivers what is promised; holds self and others accountable for results, commitments and behaviors Takes appropriate accountability for failure; does not blame others Takes action in a timely manner, with urgency or caution as appropriate, but always in a planful way Balances short-term and long-term priorities and maximizes the opportunities for both Addresses organizational or cultural barriers that could prevent success Make Difficult Decisions Identifies crisis situations and elevates appropriately Encourage an Open Environment and Knowledge Sharing Provides accurate, frequent and constructive feedback to subordinates, peers and leaders Openly shares information with peers Challenges and expects to be challenged Supervisory/Management Responsibilities Direct Reports : None (individual contributor) Indirect Reports: None (individual contributor) Minimum Education Bachelor's Degree in pharmacy, biology, chemistry, pharmacology, or related subject Minimum Experience/Training Required 10+ years’ experience in Regulatory Affairs, R&D, Manufacturing or related area. By exception, less experience is acceptable, e.g. if supplemented by other relevant knowledge such as a higher degree in a related discipline.

Job location -Belguim Pharmacist for Belgium Full job description Key Responsibilities: Dispense Medications: Accurately dispense prescription medications to patients, ensuring correct dosage, labeling, and documentation in compliance with regulatory standards. Patient Counseling: Provide comprehensive counseling on medication use, including dosage instructions, potential side effects, drug interactions, and storage recommendations. Medication Management: Monitor and manage medication therapy, ensuring that patients are adhering to their prescribed treatment plans and adjusting therapies when necessary. Collaborate with Healthcare Teams: Work closely with physicians, nurses, and other healthcare professionals to ensure the proper selection and administration of medications. Review Prescriptions: Verify prescriptions for accuracy, potential drug interactions, and contraindications, resolving any issues with the prescriber if necessary. Inventory Management: Oversee the ordering, storage, and stocking of medications, ensuring that supplies are maintained in compliance with legal and safety standards. Regulatory Compliance: Ensure adherence to all local, state, and federal regulations related to the dispensing of medications and the operation of a pharmacy. Pharmacovigilance: Monitor patients for adverse drug reactions and report these to the relevant authorities as required. Patient Education: Provide information on health conditions, disease prevention, and the proper use of non-prescription products. Quality Assurance: Participate in pharmacy quality improvement initiatives and contribute to the development of policies and procedures for safe and effective medication use. Qualifications: Education: Bpharm/Dpharm degree or equivalent from an accredited institution. Licensure: Valid pharmacist license required Experience: Prior experience in a retail, hospital, or clinical pharmacy setting preferred. Skills: Strong attention to detail and accuracy. Excellent communication and interpersonal skills. Ability to work independently and as part of a team. Strong organizational and time-management skills. Knowledge of drug therapy, pharmacology, and medication safety practices. Work Environment: Work may be performed in a retail pharmacy, hospital, or clinic setting. May involve standing for long periods and interacting directly with patients and healthcare providers. Ability to manage a fast-paced, high-pressure environment with a focus on patient safety and care. Key Competencies: Attention to Detail: Ensure accuracy in prescription dispensing and patient records. Communication: Effectively communicate with both healthcare professionals and patients. Problem Solving: Identify and resolve medication-related issues. Ethical Judgment: Uphold ethical standards in medication dispensing and patient care. Job Type: Full-time Pay: ₹15,000.00 - ₹20,000.00 per month Schedule: Day shift Education: Bachelor's (Preferred) License/Certification: PHARMACY REGISTRATION CERTIFICATE (Require) .Contact @ +91 8281914152 Job Types: Full-time, Permanent Pay: ₹18,086.00 - ₹30,419.22 per month Benefits: Health insurance Schedule: Day shift Morning shift Rotational shift Supplemental Pay: Commission pay Overtime pay Performance bonus Shift allowance Yearly bonus Education: Diploma (Required) Experience: Basic computer: 1 year (Required) total work: 1 year (Required) Pharmacist: 1 year (Required) Language: English (Preferred) License/Certification: Registered Pharmacist - (Required) CFP (Preferred) Work Location: In person

Job Description: We are seeking a qualified B.Pharmacy graduate to manage daily pharmacy operations. The ideal candidate will have a strong understanding of medications, prescriptions, and patient care. Key Responsibilities: Dispense prescribed medicines accurately. Review prescriptions for accuracy and legality. Advise patients on proper medication usage. Maintain stock levels and expiry checks. Ensure compliance with pharmacy laws and regulations. Assist in inventory management and billing. Requirements: B.Pharmacy degree (mandatory) D.Pharmacy license (if required by local laws) Basic knowledge of pharmacology and drug interactions Good communication and customer service skills Freshers and experienced candidates both can apply Job Type: Full-time Pay: ₹10,000.00 - ₹20,000.00 per month Schedule: Day shift Work Location: In person

CPC & CCS Certification Training With Placement Life sciences Graduates only in Medical Coding Freshers * Must be certified (CPC/CCS) from AAPC or AHIMA * Strong knowledge on Human Anatomy, Physiology Offline - KPHB @Hyderabad Call - 9052442000

This role is for one of our clients Industry: Hospitals and Health Care Seniority level: Associate level Min Experience: 2 years Location: Durgapur JobType: full-time About the Role We are seeking a clinically adept and empathetic Anesthesiologist to become an integral part of our surgical and critical care team. In this role, you will be responsible for the safe administration of anesthesia across a wide range of procedures and patient profiles. From pre-operative evaluations to post-anesthesia care, your work will directly impact patient comfort, surgical outcomes, and safety. You’ll collaborate with surgeons, intensivists, and perioperative staff to develop customized anesthesia plans and respond swiftly to evolving intraoperative conditions. This is a high-responsibility role that demands attention to detail, rapid decision-making, and a deep understanding of patient physiology. Key Responsibilities Pre-Operative Evaluation Conduct detailed pre-anesthesia assessments including patient history, comorbidities, and risk stratification. Recommend suitable anesthesia techniques based on the planned procedure and patient condition. Counsel patients and obtain informed consent for anesthesia. Anesthesia Administration & Monitoring Administer general, regional, spinal, epidural, or sedation anesthesia using best practices and safety protocols. Continuously monitor patient vitals, adjust anesthetic depth, and manage intraoperative hemodynamics and ventilation. Ensure smooth induction, maintenance, and emergence from anesthesia. Post-Operative Care & Pain Management Provide post-anesthesia recovery monitoring and manage common complications such as nausea, hypotension, or respiratory depression. Prescribe and oversee pain management strategies including PCA (patient-controlled analgesia) and nerve blocks. Participate in post-op rounds and address anesthesia-related patient concerns. Operational & Safety Protocols Ensure all anesthesia machines and monitoring equipment are calibrated and in proper working order. Follow institutional guidelines for infection control, sterile procedures, and emergency preparedness. Maintain detailed, timely, and legally compliant anesthesia records for each case. Team Collaboration & Training Collaborate effectively with surgeons, ICU staff, and nurses to deliver integrated perioperative care. Train nursing staff and junior medical personnel in basic life support and airway management when necessary. Contribute to clinical audits and quality assurance initiatives in the anesthesiology department. Required Qualifications & Skills MBBS with MD/DNB in Anesthesia from an accredited institution. 2–5 years of hands-on experience in a hospital setting, preferably in multi-specialty or tertiary care. Proficient in airway management, regional blocks, and crisis response protocols. Strong grasp of anesthetic pharmacology, patient physiology, and monitoring tools. Ability to manage both elective and emergency surgical cases confidently. Calm and precise under pressure, with excellent interpersonal communication. Preferred Attributes Certified in ACLS/BLS or equivalent life support programs. Prior experience in ICUs or critical care settings. Exposure to a broad case mix across general surgery, obstetrics, orthopedics, and laparoscopic procedures. Willingness to work in rotational shifts, on-calls, and during emergencies as required.

Urgent vacancies for, Assistant professor,Associate professor , with good experience in medical college at a medical college in mathura Salary as per industry Norms,

Continental Hospitals, Gachibowli, Hyderabad Continental Hospital is a JCI and NABH accredited facility offering multi-specialty, tertiary, and quaternary care services with more than 56 specialties, the healthcare institution is spread across 18 floors (1.4 million sq. ft), located in the IT and Financial District of Hyderabad, Gachibowli. Continental Hospitals was founded by Dr Guru N Reddy in April 2013 to redefine healthcare in India by providing quality patient care with integrity, transparency, a collaborative approach, and evidence-based medicine Continental Hospitals, India’s first LEED qualified super specialty hospital is built on international standards and is designed to enhance the healing spaces with natural ventilation, safety, and privacy. The hospital has incorporated the safest standards in the world including fire, water resources, sanitation, and internal transportation systems. Continental Hospitals has a special health check lounge and a dedicated area for international patients, state-of-the-art facilities and medical equipment, as well as the latest communication and information technology. Key specialties include Gastroenterology, Oncology, Orthopedics, Neuroscience, Cardiology, and Multi-organ Transplants. Our proactive team of highly experienced doctors, nurses, and staff ensures that we deliver the highest standard of personalized care to our patients at all times. Job Title: Senior Clinical Pharmacologist Department: Clinical Pharmacy Services / Pharmacy & Therapeutics Location: Continental Hospitals, Financial Distt, Nanakramguda Role Summary: We are seeking an experienced and highly competent Clinical Pharmacologist with a minimum of 8 years of proven experience in a multispecialty hospital environment. The ideal candidate will play a key role in ensuring safe, effective, and evidence-based medication use, supporting patient care through clinical expertise and active collaboration with the medical team. Key Responsibilities: Medication Safety: Implement and monitor medication safety protocols to reduce errors and enhance patient safety. Medication Reconciliation: Conduct thorough medication reconciliation during patient admission, transfer, and discharge to avoid discrepancies. Medication Therapy Management (MTM): Evaluate and optimize medication regimens in collaboration with physicians to ensure therapeutic effectiveness and minimize risks. Adverse Drug Event (ADE) Reporting: Identify, document, and report adverse drug reactions and medication errors per hospital and regulatory protocols. Medication Management: Oversee appropriate storage, usage, and administration of drugs across clinical departments in compliance with regulatory guidelines. Therapeutic Drug Monitoring: Monitor and adjust dosages for high-risk medications (e.g., antibiotics, anticoagulants) based on pharmacokinetic and lab data. Prescription Auditing: Audit prescriptions for accuracy, appropriateness, interactions, and compliance with hospital formulary and guidelines. Drug Dose Calculations: Ensure correct dosage calculations, especially for pediatric, geriatric, renal, and critical care patients. Protocol Development: Participate in the development and review of drug use protocols, clinical pathways, and standard treatment guidelines. Case & Seminar Presentations: Prepare and deliver case studies, clinical reviews, and seminars to enhance pharmacy and interdisciplinary knowledge. Required Qualifications & Experience: Education: M. Pharm / Pharm. D (Doctor of Pharmacy) Experience: Minimum 8 years of experience in a clinical pharmacy role within a multispecialty hospital Licensure: Registered with State Pharmacy Council Key Competencies: In-depth knowledge of pharmacology, clinical therapeutics, and drug interactions Strong analytical and problem-solving skills Excellent communication and presentation abilities Commitment to patient-centered care and interdepartmental collaboration Familiarity with EMR systems and pharmacy informatics tools Preferred Certifications: Certification in Clinical Pharmacy Practice / Pharmacovigilance Advanced training in MTM or Medication Safety (preferred)

Private Medical colleges in Various Locations in India have requirement of Pre Para clinical faculty

Private Medical colleges in india have requirement of pharmacology assistant and associate and professor onroll requirement monthly best payment option.

Private Medical colleges in india have requirement of pharmacology assistant and associate and professor onroll requirement monthly best payment option.

We are looking for an Associate Content Editor to join our Experimental Pharmacology & Models team in Chennai. This is an amazing opportunity to work on Cortellis Drug Discovery Intelligence (CDDI). This is a small talented creative team and reporting to the Team Manager. We have a great skill set in Life Sciences and we would love to speak with you if you are interested in a stimulating growth-oriented position and a challenging career. About You – M Pharm, B. Pharm Graduates. 0 to 2 years experience in pharmacology content Knowledge in content analysis & editing What will you be doing in this role? To review/analyze and update the Pharmacological Activities and to update the internal core database (CMS) according to the guidelines proposed. To review/analyze and update IN VITRO, IN VIVO and EX VIVO study from patents, references, posters, and conferences in CMS Pharmacological parameters and units measured, materials and the methods used in the respective activities from patents, references, posters, and conferences Pharmacological details of the drug including the animal model, dose regime, end point measurements and duration of the drug Achieve production volume and quality targets Recording of performance against target Taking an active role within the team to ensure targets are met Maintain awareness of current developments in own technology areas Achieve and maintain consistent quality standards, Effective personal planning, and time management Maintain a flexible and adaptable approach towards process change To take responsibility for identifying technology training and developmental needs for yourself on an on-going basis To make positive efforts to promote personal safety and that of others by taking reasonable care at work, by carrying out the requirements of the law or following recognized codes of practice provided or advised by management to ensure safe working practices To undertake any other reasonable duties as requested by your line manager / director on a permanent or temporary basis. Product Cortellis Drug Discovery Intelligence focuses exclusively on pharma and drug development, harmonizing and integrating essential biological, chemical, and pharmacological data from disparate sources into a single platform. Users will be benefited by using the broadest, deepest, most accurate source of R&D intelligence that has been manually curated, validated, and shared using a solution built by scientists for scientists. About The Team Experimental Pharmacology & Models team analyze journals, patents and meeting abstracts and provides content to CDDI. Content includes pharmacological activity data for therapeutic drugs and experimental models in which a human disease is modelled, looking for a treatment. External stakeholders would be scientists interested in researching the details of specific diseases. Hours of Work 40 hours/per day 9:00 AM to 6:00 PM IST. This is a full-time position Location- Chennai At Clarivate, we are committed to providing equal employment opportunities for all qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.

We are looking for an Associate Content Editor to join our Experimental Pharmacology & Models team in Chennai. This is an amazing opportunity to work on Cortellis Drug Discovery Intelligence (CDDI). This is a small talented creative team and reporting to the Team Manager. We have a great skill set in Life Sciences and we would love to speak with you if you are interested in a stimulating growth-oriented position and a challenging career. About You – M Pharm, B. Pharm Graduates. 0 to 2 years experience in pharmacology content Knowledge in content analysis & editing What will you be doing in this role? To review/analyze and update the Pharmacological Activities and to update the internal core database (CMS) according to the guidelines proposed. To review/analyze and update IN VITRO, IN VIVO and EX VIVO study from patents, references, posters, and conferences in CMS Pharmacological parameters and units measured, materials and the methods used in the respective activities from patents, references, posters, and conferences Pharmacological details of the drug including the animal model, dose regime, end point measurements and duration of the drug Achieve production volume and quality targets Recording of performance against target Taking an active role within the team to ensure targets are met Maintain awareness of current developments in own technology areas Achieve and maintain consistent quality standards, Effective personal planning, and time management Maintain a flexible and adaptable approach towards process change To take responsibility for identifying technology training and developmental needs for yourself on an on-going basis To make positive efforts to promote personal safety and that of others by taking reasonable care at work, by carrying out the requirements of the law or following recognized codes of practice provided or advised by management to ensure safe working practices To undertake any other reasonable duties as requested by your line manager / director on a permanent or temporary basis. Product Cortellis Drug Discovery Intelligence focuses exclusively on pharma and drug development, harmonizing and integrating essential biological, chemical, and pharmacological data from disparate sources into a single platform. Users will be benefited by using the broadest, deepest, most accurate source of R&D intelligence that has been manually curated, validated, and shared using a solution built by scientists for scientists. About The Team Experimental Pharmacology & Models team analyze journals, patents and meeting abstracts and provides content to CDDI. Content includes pharmacological activity data for therapeutic drugs and experimental models in which a human disease is modelled, looking for a treatment. External stakeholders would be scientists interested in researching the details of specific diseases. Hours of Work 40 hours/per day 9:00 AM to 6:00 PM IST. This is a full-time position Location- Chennai At Clarivate, we are committed to providing equal employment opportunities for all qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.

Profile AIIMS-Guwahati has started a broad-based full-time research program leading to the award of Doctor of Philosophy (Ph.D.) degree from July 2024 session with an idea that research work may exemplify the development of new interventions, development of new biomarkers, testing of new scientific ideas, or gaining insight into biological processes and health sciences. The Ph.D. degree would be awarded to a candidate who will work full time as per the program regulations and will submit a thesis on the basis of original research work done by him/her in any discipline-specific or multidisciplinary area, contributing to the advancement of knowledge in Medical, Nursing, and Allied Health Sciences. The prospective candidates are also likely to innovate methods of application of existing knowledge in Medical, Nursing and Allied Health Sciences. The basic objective of the Ph.D. course is to enhance the scientific capacities of researchers and scientists in the field of Medical, Nursing, and Allied Health Sciences. The vision of the institute is to provide excellent opportunities for research work in the modern era of biomedical sciences with the developing state of art infrastructure and facilities. Duration The duration of the course shall be the time period from registration to submission of thesis. The minimum period of registration in respect of all the candidates who are registered for Ph.D. shall be three years. The maximum period of registration shall not exceed five years. Extension beyond the period of 5 years can be given for a maximum period of 6 months on the recommendation of the Doctoral Committee and final approval by the Executive Director. Further extension beyond 5 years & 6 months can also be given by the Executive Director for a maximum period of 6 months in highly exceptional circumstances (like medical exigencies, natural calamities etc.), subject to subsequent approval of the Academic Committee, and such extension may not be given retrospectively. If the thesis is not submitted within these timelines, the registration of the candidate may be summarily cancelled. Qualification Qualifications A candidate seeking admission to the program of study leading to the award of Ph.D. degree must possess at least one of the following qualifications: Medical qualification: MBBS/BDS with a minimum of 55 PERCENT aggregate marks or MD/MS/MDS/DM/MCh in the subject concerned or equivalent Diplomate of National Board of Examination degree. Candidates who have obtained any of these degrees from medical colleges that are not recognized or considered equivalent by the Medical Council of India/Dental Council of India/National Medical Commission shall not be eligible to apply. AYUSH qualification: Candidates holding a Masters degree in any branch of AYUSH (Ayurveda, Yoga and Naturopathy, Unani, Siddha, Homeopathy) recognized by the Central Council of Indian Medicine (CCIM) are eligible to be considered for admission to the PhD program. Non-Medical qualification: For non-medical candidates, eligibility shall be Masters Degree awarded by UGC-approved Indian Universities or equivalent in subjects pertaining to life sciences such as Anatomy, Physiology, Biochemistry, Biophysics, Human Biology, Molecular Biology, Microbiology, Biotechnology, Immunology, Botany, Zoology, Genetics, Molecular and Human Genetics, Human Genomics, Forensic Science, Cell Biology, Pharmacology, Pharmacy, Laboratory Technology, Speech and Hearing, and allied subjects. Candidates having BTech (Biotechnology) and MTech (Biotechnology) degree will also be eligible. For non-life science subjects, the eligibility shall be M.Sc. (Psychology/Clinical Psychology), M.A. (Psychology/Clinical Psychology), or M.Phil. (Clinical Psychology). Candidates holding masters degree in Yoga, Radiography, Radiotherapy, any branch of Engineering, Applied Psychology, and Counselling Psychology will also be eligible. Non-medical candidates should have at least 55 PERCENT marks in the last eligibility examination qualified. Candidates possessing Masters Degree through distant learning course shall not be eligible. To Apply The application for admission to the PhD program will be made available on AIIMS, Guwahati official website i.e. www.aiimsguwahati.ac.in. The link for submission of online applications along with other relevant information will be activated on the date of notification. Any Amendment/Rectification/Change/Editing in the application is NOT allowed after final submission of the application. Applicants may note that any correspondence will NOT be entertained in this regard. Inadequately filled/incomplete applications will be summarily rejected. For more details click here.

Engaging with and taking care of customers, dispensing the right medicines as per the prescriptions, ensuring optimal availability of drugs, purchasing, returning and safekeeping the physical stock of medicines including regular screening for expiry of drugs, complying with the provisions of D&C Act and other related Acts, Negotiating, and dealing with suppliers etc

Contact no. 8810527696 *Explore Exciting Opportunities in Clinical & Non-Clinical Medicine Across India!* We're hiring for various positions in *All Clinical and Non- Clinical Profiles* across multiple locations in India! 1. *Assistant Professor* 2. *Associate Professor* 3. *Professor* 4. *Senior Resident* *PAN India Locations:* Explore new horizons in your medical career across various cities in India! *How to Apply:* Call/WhatsApp: * 8810527696 * Email: hr8pathfinders@gmail.com *Dual Career Support:* Share your spouse's CV if they're a medical professional (clinical or non-clinical). References are also appreciated! *Help Us Spread the Word!* Circulate this announcement within your networks and help your peers discover these amazing opportunities. *Best Regards,* *HR. Jaishree* *8810527696* Pathfinders Global (P) Ltd _Let's shape the future of healthcare together!_

Clove Dental is looking for Oral Surgeon Professional to join our dynamic team and embark on a rewarding career journey A surgeon is a medical doctor who specializes in performing surgical procedures to treat injuries, diseases, and deformities through operative techniques Surgeons undergo extensive training, typically completing medical school followed by a residency program focused on surgery They possess advanced knowledge of human anatomy, physiology, and medical technology Surgeons work in various specialties such as general surgery, orthopedic surgery, neurosurgery, cardiovascular surgery, and more Their responsibilities include diagnosing patients, planning and performing surgical procedures, collaborating with other medical professionals, and providing post-operative care Surgeons require excellent technical skills, decision-making abilities, and communication skills to effectively manage complex medical conditions and ensure the best possible outcomes for their patients

General Conditions: Before applying, candidates should ensure that they fulfil all the eligibility criteria mentioned below. Candidates applying for the post of Pharmacist / Assistant Pharmacist must submit their State Pharmacy Council Registration Certificate in order to obtain the pharmacy license for the outlet. For Pharmacist minimum 2 years of post qualification is mandatory For Assistant pharmacist 0-1 years of experience (Freshers also can apply) Salary scale : 18000 p.m to 20000 p.m Educational Qualification : B.pharm / D.pharm / M.pharm Candidates residing in Bangalore is mostly preferred. Duties and Responsibilities: 1. Dispense medicines by reviewing and interpreting physicians orders. Clarifications if any must be obtained from the prescribing doctors. 2. Prepare and maintain all the statutory and MIS registers, including but not limited to Schedule X drugs, Schedule H1 drugs, cash deposit registers, high-value item registers, suture registers, etc. 3. Compliance with all the statutory regulations prescribed by the drugs control department, the state pharmacy councils, or any other competent authorities. The pharmacist also needs to attend the audits. 4. Maintenance of medicine stock and inventory in the pharmacy involves properly stacking the items and removing expired, near-expiry, and damaged medicines from the pharmacy inventory. 5. Perform internal stock verification on a daily basis and submit the report to the management. Also to ensure that the physical stock is tallying with the book stock.

Designation & Job : Manager – Regulatory Affairs -( Chemical Industry) Function : Regulatory Affairs Work Location : Greater Noida Manager’s Manager: Head – QA & RA Reporting Manager: Head – QA & RA JOB Description Regulatory Compliance & monitoring Ensure compliance with existing domestic and international chemical regulations governing industrial chemicals, fine chemicals & specialty chemicals. Proactively monitor, evaluate business impact and communicate new and amended legislation and regulations Pre-registration / Registration of chemicals and Maintenance Responsible for preparation & filing of pre-registration and registration dossiers of chemicals under EU REACH, Korea REACH, UK REACH, Turkey REACH etc Assessment of New Product Regulatory Requirements Provide regulatory guidance/consultancy to the business and R&D teams on compliance strategies for new and existing products. Substance Volume Tracking Responsible for maintaining and monitoring the export volume of the products through the ERP system to comply with the registered volume in the respective countries. Hazard Communication Review of Safety Data Sheets & Labels of the hazardous products Education Qualification(Highest ) with Target Institute(s) Master’s degree in Toxicology, Pharmacology, Biochemistry, Chemistry or other life science Desired Certifications : A minimum of 8 to 10 years of related experience. Experience Range : 10 – 12 years No. of years post Highest Qualification : 8 years Desirable experience : 10 to 12 Years of Industrial Experience

MD Pharmacology qualified only. We also hiring Assistant Professors, Seniors Residence positions (Experience as per NMC norms). please reach out me with short CV.

Job_Description":" Preoperative Preparation: Assist anesthesiologists in preparing the operation theatre before procedures. Check, calibrate, and prepare anesthesia machines, ventilators, suction equipment, and monitors. Equipment Management: Ensure availability and proper functioning of anesthesia equipment and supplies. Maintain stock of drugs, consumables, and gases required for anesthesia. Patient Support: Assist in patient positioning and preparation under the supervision of an anesthesiologist. Monitor vital signs and support anesthetic induction procedures. Intraoperative Assistance: Provide direct support during surgeries including handling anesthesia tools, monitoring equipment, and patient response. Respond quickly to any technical issues or emergency requirements. Postoperative Duties: Assist in patient transfer to recovery area and help monitor vitals post-procedure. Clean, disinfect, and store anesthesia equipment and instruments after use. Documentation and Compliance: Maintain proper records of equipment use, maintenance, and any incident reports. Ensure adherence to infection control, OT protocols, and biomedical waste disposal standards. Requirements Knowledge of anesthesia machines, gas delivery systems, and monitoring equipment Basic understanding of pharmacology and patient safety Attention to detail and quick decision-making in critical situations Ability to work calmly under pressure Good communication and teamwork skills Familiarity with operation theatre discipline and infection control ","

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position Content Creation Subchapter Lead Roche India – Roche Services & Solutions Hyderabad A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche. Roche is a leading biotechnology company renowned for its innovative approach, offering exceptional career paths and comprehensive benefits for both fresh graduates and professionals. As we continue to expand, we seek new talents to join our transformative Roche Services & Solutions Center. Our flexible working framework includes an average of two office days per week, accommodating diverse working styles and needs. The Global Digital Hub is a growing business line within the Roche Services & Solutions Center. Our primary goal is to enhance Roche's digital capabilities globally by supporting central initiatives in areas such as Social Media Management, Brand Support, Digital Publishing Services, Marketing Automation, Content Creation, and Creative Design. Your Opportunity The Content Creation Subchapter Lead is a pivotal people leader who inspires and engages subchapter members to collaborate across the network, significantly contributing to Roche’s Ten Year Ambitions. This role is accountable for driving the integration of the new operating model, exemplifying agile collaboration. The content creation chapter team consists of medical writers, content editors, project delivery coordinators, and medical copy quality assurance specialists. As the Content Creation Subchapter Lead, you will be responsible for supporting the strategic vision and direction of the chapter, continuously seeking opportunities for innovation and value creation. This critical position has a global scope, leading a diverse team across various regions. People Leadership: Lead, mentor, and develop team members, providing coaching and support to enable them to execute content creation projects successfully and continuously improve their skills. Create and implement personal development plans tailored to individual needs and aspirations. Operational Leadership: Coordinate the operation of the Content Creation Subchapter, ensuring high effectiveness of assigned content creation activities. Manage content creation resources, monitor their utilization, and ensure customer satisfaction within the subchapter. Recruitment: Find, attract, develop, and retain top talent, aligned with the evolving needs of the function and the business. Conduct interviews and facilitate the onboarding process. Capability Building: Foster the development of the content creation team members, promoting a culture of continuous learning, innovation, and content excellence. Agile Collaboration: Drive the embedding of the new operating model, serving as a role model for agile collaboration within the content creation subchapter. Cross-Functional Leadership: Collaborate effectively with different chapters, subchapters, and other relevant teams to drive impactful content creation solutions and align with business and Global Digital Hub strategies. Service Quality: Provide recommendations to enhance service quality, responsiveness, and content output to meet or exceed business partners' expectations. Process Governance: Establish and maintain process governance principles, ensuring proper documentation and adherence to content creation best practices within the scope of the Content Creation Subchapter's responsibility. Stakeholder Engagement: Professionally represent the Content Creation Subchapter with key stakeholders, promoting the value and impact of content creation within the organization. OneRoche Mindset : Support the embedding of the OneRoche mindset within the content creation subchapter and across the Global Digital Hub, fostering a culture of innovation and collaboration. Who You Are We are looking for a dynamic individual who is highly involved and passionate about medical copy and content services. As a Content Creation Subchapter Lead, you thrive in a team environment and excel in a fast-paced global setting. You are a proactive and innovative problem-solver, always seeking sustainable and scalable solutions. Keeping up with the latest digital updates and content trends is a natural part of your commitment to providing cutting-edge content capabilities to our partners You hold a Master’s degree or PhD in (Life Sciences), Medicine, Dentistry, Pharmacy/Pharmacology, Microbiology with 8+ years of experience with 4+ years of experience working in project management roles, preferably within large organizations, agencies, or startups 3+ years of experience in people development, coaching, and leadership, specifically within a content creation context A higher degree in life sciences is highly preferred, but candidates with other relevant experience will also be considered. Strong medical or science background High level proficiency in English, with excellent written and verbal communication skills Ability to work within a team and in different time zones Customer-service mentality & can-do attitude Experience with the standard IT applications, preferably including Google suite Continuous improvement and growth mindset Ability to work in a fast-paced and changing environment, ability to prioritize tasks Strong problem-solving skills, including analytical abilities, active listening, critical thinking, and a focus on sustainable and scalable content solutions Ability to thrive under pressure, manage complex challenges, and work independently while maintaining high content standards Quick learner with a passion for exploring new technologies, tools, and techniques Dynamic and flexible in adapting to different software and workflows Excellent interpersonal skills to foster collaboration within the team and effectively engage with senior leaders and stakeholders Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer.

Qualification : Diploma in Pharmacy Experience : 2 to 3 Years (Hospital Experience) Job Location : Barabanki (U.P) Job Type : Full-Time Job Summary: We are seeking a licensed and detail-oriented Pharmacist to join our team. The Pharmacist will be responsible for dispensing medications, providing pharmaceutical care, ensuring accurate prescription fulfillment, and advising patients on the safe and effective use of medications. Key Responsibilities: Review and interpret physician prescriptions for accuracy, dosage, and possible drug interactions. Dispense prescription and over-the-counter medications in accordance with legal and professional standards. Provide counseling and education to patients on medication usage, side effects, interactions, and storage. Ensure proper storage, handling, and disposal of pharmaceutical products. Monitor patient medication therapies to improve outcomes and prevent adverse drug reactions. Collaborate with healthcare professionals to optimize patient care. Maintain accurate patient records, inventory, and reports. Comply with all regulatory and safety standards (e.g., HIPAA, FDA, DEA, local regulations). Stay updated on new drug therapies, research, and developments in the pharmaceutical field. Qualifications: Diploma in Pharmacy from an accredited institution. Valid and current pharmacy license in U.P. Proven experience as a pharmacist (e.g., retail, hospital, or clinical). In-depth knowledge of pharmacology, pharmaceutical law, and ethics. Job Type: Full-time Pay: ₹12,000.00 - ₹20,000.00 per month Benefits: Cell phone reimbursement Health insurance Paid sick time Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person

Drug Discovery - In Vitro Pharmacology: Ph.D. in Bio-chemistry / Molecular Biology / Pharmacology / Biotechnology with 10 years industry experience or Ph.D. + post-doctoral fellowship with 6-8 years in drug discoveryresearch. Knowledge: Good understanding of overall drug discovery process; exposure to multiple therapeutic a reas In-depth understanding of all aspects of in vitro pharmacology as applicable to new drug d iscovery Basicunderstanding of biologics development like mAbs, ADC, etc Skills: Ability toestablish cost effective biochemical and cell based assays by using differentkinds of readouts like absorbance, luminescence, fluorescence and HTRFtechnologies. Ability to screenNCEs in biochemical and cell based assays Statistical applications and dataanalysis Good communication and management skills Competencies: Expertise and specializationin developing target based biological assays for NCEs and their screening Ability toinitiate, test and adapt new assay and screening methodologies Focused; driven to finish set goals within strict timelines