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Monday, 7 November 2016

Hindustan  Aeronautics  Ltd  (HAL),  a  Navratna  Central  Public Sector  Undertaking,  is  a  premier  Aeronautical  Industry  of  South East  Asia,  with  20  Production/Overhaul/  Service  Divisions  and  10 co-located R&D Centers spread across the Country. HAL’s spectrum of  expertise  encompasses  design, ...
Job Description: The roles and responsibilities of the Trainee Scientific Writing include the following:· Following the specifications for documentation, both client or company provided· Maintaining records for all assigned projects, including archiving· Ensuring getting feedback from customers and supporting implementation of customer management tactics· Controlling/reducing the cost of content development, cycle time, and error rates in projects·...
HLL Lifecare Limited is a Mini Ratna Company of Govt. of India under the Ministry of Health & Family Welfare. HLL, a Schedule-B Public Sector Enterprise is today a multi product, multi unit organization addressing various public health challenges. The Company with seven manufacturing units and marketing offices throughout the country is engaged in the manufacturing and marketing of a wide range of contraceptives and healthcare products....
 Job Description: End to End CDM activities Relevant experience in Clinical Data Management Perform data management activities on the assigned project in a timely and efficient manner Generate queries to clarify and improve the quality of the data Test and execute validation procedures Apply n...
Job Description To provide medical support to marketing team in strategizing brand plans and sales team. Providing scientific and medical input to  Product Management Team for development of visual aid, LBLs, Recent guidelines, Treatment algorithms, Reference folders and patient education literature. Conduct medical and orientation programme on Anatomy, Physiology , various related Clinical conditions and Product based knowledge to...

Thursday, 27 October 2016

Freshers opening as Research Investigator in Biotransformation @ SyngeneJob DescriptionPrincipal Accountabilities :Project Responsibilities: Provide comprehensive biotransformation support to assigned programs starting from carrying out experiments, analyzing data, preparing presentations, discussing with key stakeholders and presenting to the discovery team. Participating in relevant meetings and proactively proposing experiments to understand...
Opening for Laboratory Quality Assurance @ Zydus CadilaJob Description    Experience: 3 to 5 yrsQualification: M.PharmaTo prepare / review Chemical and Microbiological analytical method validation, Transfer and Verification protocol and report.To review RM/PM specification, in-process specification, finished product specification, shelf life specification and its relevant MOA.To review Testing work sheet of RM/PM, In-process, finished...
Vacancies for Associate Scientist @ Novartis Job Description 1. Actively participate in project teams/meetings/networks 2. Meet quality, quantity and timelines in all assigned projects. 3. Plan, organize, perform and document DS/DP related analytical activities including release/stability testing, method development/validation etc. under minimal guidance from more experienced team member 4. Provide efficient and robust processes for the analysis of DS/DP under adequate guidance from more experienced team members. 5. Provide raw data...
Walk in interview for B.Pharm, M.Pharm as Trainee Medical Coder @ Omega Healthcare Post: Medical Trainee CoderJob DescriptionUnderstand the client requirements and specifications of the project and code the charts accordinglyEnsure that the deliverables to the client adhere to the quality standardsPrepare and maintain status reportsQualification:Eligibility criteria Following Life science and non-life science candidate will be considered....

Wednesday, 26 October 2016

On line applications are invited for the Posts of the Scientific Officer (Biology), Class-II, in General State Service under the Director of Forensic Science, Home Department (Advt. 47 /2016-17) between date: 18/10/2016, 13.00 Hrs. to date 03/11/2016, 13.00 Hrs. How to Apply : On line applications are invited for the Posts of the Scientific Officer (Biology), Class-II, in General State Service under the Director of Forensic Science, Home Department...
Claris Otsuka Private Ltd. (Claris Otsuka) is a Joint Venture between Claris Lifesciences Ltd., India, Otsuka Pharmaceutical Factory, Inc., Japan, and Mitsui & Co. Ltd., Japan, for Claris’ Infusion Business in India and Emerging Markets. We primarily manufacture & market products across multiple markets and therapeutic segments. Being a leader in intravenous nutrition products, we are committed to being the best partner of patients...
Application in plain paper is hereby invited for filling up the following posts on contractual basis at a fixed pay as shown against each for District Health & Family Welfare Society, South Tripura. It will be purely contract basis for a period of 11 (Eleven) months likely to be extended based on performance of employees till the project period only. Post : Pharmacist (Alio.) Apply no...
GlaxoSmithKline Pharmaceuticals Ltd. (GSK Rx India) is one of the oldest pharmaceuticals company and employs over 5000+ people. Globally, we are a £ 27.4 billion, leading, research-based healthcare and pharmaceutical company. In India, we are one of the market leaders. At GSK, our mission is to improve the quality of life by enabling people to do more, feel better and live longer. This mission drives us to make a real difference to the lives of...
Job Description Immediate Openings for IP-DRG Medical Coding -  @ Vee Technologies Job Description: 2+ Years of experience in IP-DRG Coding.Coding certification like CIC, CPC, CCS, CPC-H, CCS-P. is added advantage.Apply no...
Job Description End to End Case processing in Safety database (Argus)/ application including Case Narrative writing/ medical writing in accordance with source data.  Processing of Spontaneous, regulatory, clinical trial and literature cases/ all type of case reports Seriousness and Listedness (expectedness/ event labeling) assessment Coding of events, drugs, medical history and lab test as per MedDRA & WHO dictionary. Reconciliations...
"Artemisinin treats malaria faster than any other drug. It can clear the pathogen from the bloodstream within 48 hours," says senior author Shashi Kumar, of the International Centre for Genetic Engineering and Biotechnology in New Delhi, India. "Our research is focused on finding a way to make this drug available to more people." Malaria infects more than 200 million people every year, according to the World Health Organization, and kills more than...
Thermo Fisher Scientific, the world leader in serving science announced the expansion of its Fisher BioServices cryogenic service capabilities in Japan. This expansion enables its customers to seamlessly conduct clinical trials across multiple geographies and provides patients around the world with access to life changing therapies. As a leading service provider to the cell and gene therapy community, Fisher BioServices is uniquely positioned...

Tuesday, 25 October 2016

The Central Pollution Control Board (CPCB) of India is a statutory organisation under the Ministry of Environment, Forest and Climate Change (MoEF&CC). It was established in 1974 under the Water (Prevention and Control of pollution) Act, 1974. CPCB is also entrusted with the powers and functions under the Air (Prevention and Control of Pollution) Act, 1981. It serves as a field formation and also provides technical services to the Ministry...
Institute of Good Manufacturing Practices India, registered as a non-profit society with Government of India and approved (as a higher/professional Education Institute) by Quality Council of India(QCI) – which is an autonomous body and an accreditation authority for education & vocational training providers under the Department of Industrial Policy & Promotion, Ministry of Commerce & Industry, Government of India -presents...
Biocon is an integrated biotechnology enterprise focused on the development of biopharmaceuticals. With successful initiatives in drug discovery and development, bioprocessing, manufacturing and global marketing, Biocon delivers products and solutions to partners and customers in over 75 countries. Biocon has the defining science, world class capabilities and a focused vision to deliver the promise of innovative and affordable medicine to a waiting...
On line applications are invited for the Posts of the Scientific Officer (Biology), Class-II, in General State Service under the Director of Forensic Science, Home Department (Advt. 47 /2016-17) between date: 18/10/2016, 13.00 Hrs. to date 03/11/2016, 13.00 Hrs. Post : Scientific Officer Apply no...
Job Description1. Need to do literature search for new projects and for writing patents.2. market research for new products3. Documentation4. SOP write up5. Identification of materials suppliers and manufacturers, specification and material status. Forward your CV to : hr1.vsp@gmail.com &nbs...
Job Description:Clinical Scientific Expert II is responsible for ensuring the collection, review/ reporting of high quality trial data, and study reporting/publishing in compliance with Novartis processes, GCP/ICH and regulatory requirements. In addition, Responsible for ensuring high quality scientific inputs to the clinical development process and support program level activities as assigned.• In collaboration with Trial Statistician, support...
Job Description: Locally coordinate and take responsibility for trial level programming activities (analysis datasets, pooled datasets, listings, tables and figures) of individual Phase I-IV clinical trials to support program programmers and statistician in project level activities. Be responsible for statistical tasks on assigned clinical trials e.g. RAP. Maintain efficient interfaces with internal and external...
Job Description Write & review regulatory submissions like IND, IMPD, MAA, NDA, DMF and documents for regulatory advices. Guidance to cross functional teams on regulatory expectations for US, EU, Japan and major markets. Ensuring regulatory compliance in cross functional teams and managing cross functional team deliverables.\ Review of CMC, clinical, bioanalytical development related documents & ensure compliance to CTD...

Monday, 24 October 2016

 Job Description :  To work with a variety of medical records and assigns appropriate codes based on medical documentation using CPT-4 and/or ICD-9 and ICD-10 coding guidelines Handle a team of 50 medical coders and responsible for their deliverables. Develop training materials and update the contents that are relevant to the specialty. Job Requirement : 6+ years of team handling...
Job Description Warm Greetings from Visionary RCM @coimbatore !!! Immediate Requirement for Freshers in Medical Coding in Visionary RCM Infotech Coimbatore location US Healthcare process What is Medical Coding??? Medical coding is the transformation of healthcare diagnosis, procedures, medical services, and equipment into universal medical alphanumeric codes. The diagnoses and procedure codes are taken from medical record documentation,...
Job Description Prepare and procure documents for clinical dossiers for DCGI and/or USFDA submission; as applicable Prepare dossiers for EC submission Assist PM in site selection process and document collection Facilitate and coordinate with investigator and site for EC submission and approval Prepare Confidentiality Disclosure Agreement (CDA), Feasibility Questionnaires and Clinical Study Agreement (CSA) with investigators in collaboration...
Job Description  Report preparation [e.g. Periodic Safety Update Reports (PSURs), Addendum PSURs, Bridging Reports, PSUR Line Listings, US PADERs] from aggregate data for products, in accordance with client conventions and requirements;Quality checks of aggregate reports; Signal detection-related analyses and reports including cumulative analyses, issue event analyses, Drug Safety Reports , review of published literature...
Job Description 1.Responsible for authoring regulatory/ safety documents such as Protocol, CSR,PBRER/PSUR, Subject Narratives, Aggregate Reports, RMPs and others 2.Responsible for the entire life cycle of the document and accountable for maintaining quality and timeliness, and compliance to internal/client SOPs and regulations 3.Ensure that clinical documents adhere to current global standards, FDA, ICH and GCP guidelines and are in accordance...
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