Responsibilities Critically analyses large numbers of articles from biomedical published literature and internal drug safety alerts and identifies individual case safety reports (ICSRs) as well as other potential safety-relevant information impacting the risk-benefit and/or safety profile of customer’s products, as per applicable regulatory requirements and standard operating procedures. Write brief narratives summarizing the ICSR criteria and other potentially safety-relevant information in each article. Demonstrates understanding of client’s drugs labels and uses that knowledge effectively when performing the safety assessments. Completes drug safety reviewing of each biomedical literature batch in a timely, thorough, and accurate manner in accordance with client’s standards of timeliness and quality. Uses drug safety system to track all actions and assessments in an audit-ready reference history. Selects articles specific to client’s interest for inclusion in client's product literature database per guidelines. Writes accurate, detailed, and complete abstracts of selected articles using good judgement regarding the level of detail required and excellent organization, grammar, and syntax. Extracts key points of articles and creates comprehensive and detailed indexes of the abstract contents to ensure precise and complete retrieval of literature from client’s database. Ensures timely completion of indexing and abstracting of articles for assigned drugs in accordance with regulatory submission deadlines.     Qualification & Experience Master’s Degree in life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics etc.) At least 5 years of experience reviewing biomedical literature for adverse event reporting OR equivalent combination of education and experience (i.e., an information science degree with at least 5 year of relevant working knowledge of supporting drug and patient safety)  

Responsibilities Critically analyses large numbers of articles from biomedical published literature and internal drug safety alerts and identifies individual case safety reports (ICSRs) as well as other potential safety-relevant information impacting the risk-benefit and/or safety profile of customer’s products, as per applicable regulatory requirements and standard operating procedures. Write brief narratives summarizing the ICSR criteria and other potentially safety-relevant information in each article. Demonstrates understanding of client’s drugs labels and uses that knowledge effectively when performing the safety assessments. Completes drug safety reviewing of each biomedical literature batch in a timely, thorough, and accurate manner in accordance with the client’s standards of timeliness and quality. Uses a drug safety system to track all actions and assessments in an audit-ready reference history. Select articles specific to the client’s interest for inclusion in the client's product literature database per guidelines. Writes accurate, detailed, and complete abstracts of selected articles using good judgment regarding the level of detail required and excellent organization, grammar, and syntax. Extracts key points of articles and creates comprehensive and detailed indexes of the abstract contents to ensure precise and complete retrieval of literature from client’s database. Ensures timely completion of indexing and abstracting of articles for assigned drugs per regulatory submission deadlines. Maintains an awareness of new drugs and therapeutic categories, new disease entities, and changes in biomedical terminology in the published literature. Participates in other duties such as searches and terminology maintenance according to business needs and per the training provided.   Qualification & Experience Master’s Degree in Life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics etc.) At least 1 year of experience reviewing biomedical literature for adverse event reporting OR equivalent combination of education and experience (i.e., an information science degree with at least 1 year of relevant working knowledge of supporting drug and patient safety) Writing skills to support the creation of succinct, accurate, and precise summaries and working knowledge of biomedical terminology, drugs, and therapeutic areas.  

Responsibilities Do Literature search for a given step(s) / molecule (STN/Sci finder) Organize for relevant patents and papers from literature Develop a most economical / eco-friendly commercially viable technology at bench scale Co-ordinate with Analytical members and prepare reports like safety Upscale developed technology at Kilo Lab/ Pilot /Plant Scale and to take care of up-scaling problems     Qualification & Experience MSc- 3+ Yrs of Exp Phd -1-2 Yrs of Exp  

Responsibilities Europe/Australia/ Canada Drug Dossier Authoring, Reviewing & Submission drug product dossier application (EU/UK/AU/CA) Product life cycle management (LCM) activities Assessment ofpost approval changes eCTD publishing Thorough knowledge of CMC and Module 1 requirements Preparation & Submission Authoring and review & submission of new dossier application, variation, renewal and RFI for EU (DCP/MRP/NP), UK, Australia & Canada Health Authority Authoring of Module 1 along with quality modules Assessments of post approval changes, life-cycle maintenance and ensure timely post approval regulatory activities Coordinate with cross-functional teams for desired regulatory data and accordingly plan & complete regulatory filing activities Review and finalization of artwork/label as per current QRD guideline Regulatory Intelligence and develops up-to-date knowledge with regard to technical guidelines and regulatory requirements, as well as technical trends eCTD publishing Coordination Interface with R&D and other business functions on a regular basis to ensure project-specific regulatory strategy is met as agreed in timely manner Co-ordination with API vendors to resolve technical quires w.r.t. regulatory requirements To review technical documents like process validation, AMV, Stability and composition etc. received from Site QA or R&D/ADL against DMF/Dossier requirements Reporting & Maintenance Maintain regulatory files/database

Responsibilities Principle Accountabilities Case processing / data entry and related activities in the Argus safety database as per DE conventions within specified timelines. Participate in downloading, triaging, uploading and book-in of regulatory and EMA MLM ICSR reports. Participate in triaging and book-in of literature reports. Triage, Case book-in, data entry & archiving. Ensure use of PV-MedDRA for coding adverse reactions Documentation Ensure that pharmacovigilance SOPs, procedures, processes, and guidelines are adhered to communicate with external and internal customers in a timely manner, as per the requirement. Statutory Compliances Maintain an awareness of current legislation associated withthe Worldwide Regulatory Pharmacovigilance requirements. Ensures regulatory compliance by providing timely, quality information for aggregate reports and signal review following SOPs and regulations.  

Qualification & Experience MBBS 2-5 years of experience.   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Qualification & Experience GNM / BSC 5-10 years of experience in ICU/Ward/ER and HDU.   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Prevent the payment of potentially fraudulent and/or abusive claims utilizing medical expertise, knowledge of CPT/diagnosis codes, CMC guideline along with referring to client specific guidelines and member policies Adherence to state and federal compliance policies and contract compliance Assist the prospective team with special projects and reporting Work is frequently completed without established procedures Works independently May act as a resource for others May coordinate others' activities Comply with the terms and conditions of the employment contract, company policies and procedures, and any and all directives (such as, but not limited to, transfer and/or re-assignment to different work locations, change in teams and/or work shifts, policies in regards to flexibility of work benefits and/or work environment, alternative work arrangements, and other decisions that may arise due to the changing business environment). The Company may adopt, vary or rescind these policies and directives in its absolute discretion and without any limitation (implied or otherwise) on its ability to do so     Qualifications & Experience Medical degree - BHMS/BAMS/BUMS/BPT/MPT B.Sc Nursing and BDS with 1 year of corporate experience Experience Range - 06 months - 3 years (Fresher's in BPT / MPT / BHMS/ BAMS/ BUMS can also apply) Extensive work experience within own function. Proven attention to detail & Quality focused Proven good Analytical & comprehension skills Claims processing experience Health Insurance knowledge, managed care experience Knowledge of US Healthcare and coding Medical record familiarity

Responsibilities Coordinates and supervises department operation. Stocking of nutrition products and other medications safely and properly and medicines are arranged from outside stores when it is required at emergency when the stock is not available in the in house pharmacy. Overseeing organizational medicine list and medical use Review annually medication list for the patient safety and efficacy Procurement of medicines Selection of good quality product To receive the quotation from the different company for the better rates to the organization. As per doctor requirements to check the comparative rates. Negotiation for scheme with supplier/manufacturer for the approved medicines Supervises departmental personnel including: hiring, orientation, determining workload and delegating assignments, training, monitoring, scheduling and evaluating performance, and initiative corrective and disciplinary actions. Prepares and dispenses medicines, chemicals and pharmaceutical preparations according to written orders by authorized medical practitioners with clinical privileges. Assist in selection, orientates, supervises, instructs departmental personnel. Initiates and implements Quality Improvement for the department. Preparing and assign duty and duty roster for the department staff Leading pharmacy committee Audit of medicines at nursing station for their expiry and storage condition Assisting assistant pharmacist in routine work whenever required Second check on gate pass Second check on the rates are properly supplied for the rate negotiated for the organization To forward the requisition for the medical head for making available of the new drug in the organization. To inform to the prescriber for non availability of the drug in the pharmacy through a written notification and suggested for substitutions. To check the expiries are returned to the supplier credit note is receive To check the invoices of the supplier are being forwarded for the payments To monitor the proper documentation for the narcotic drug purchase sales and storage To Internalizing the S.O.P Physical stock-taking of medicines quarterly   Qualification & Experience MD/DNB/DCH Experience: 2 – 4 years   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Accountable to the In-charge OT for the delivery of standardized nursing care to patients. Assists in ensuring OT functions without disruption. – Ensures surgical, medication and patient safety. Ensures prompt safe empathic and effective care of surgical patients. Interacts empathically with family; contributes to Service Vision. Ensure medication and patient safety; adheres to infection control protocols. Complies with NABH and NE standards.   Qualification & Experience GNM/ B.Sc (Nursing) Experience: 2+   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"