Freshers opening as Research Investigator in Biotransformation @ Syngene

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...

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Opening for Laboratory Quality Assurance @ Zydus Cadila

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...

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Vacancies for Associate Scientist @ Novartis

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...

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Walk in interview for B.Pharm, M.Pharm as Trainee Medical Coder @ Omega Healthcare

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....

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Government Job "A"

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...

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Jobs for Microbiologists "A"

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...

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Pharmacists Required "A"

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...

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GlaxoSmithKline hiring Biostatistician "A"

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...

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Medical Coding jobs "A"

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...

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Sun Pharma: Executive- Global Pharmacovigilance "A"

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...

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Tobacco plants engineered to manufacture high yields of malaria drug "A"

"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...

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Thermo Fisher Scientific Expands Global Footprint to Support Cell and Gene Therapy Clinical Trials in Japan "A"

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...

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Govt Job "A"

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...

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Career in Food Industry "A"

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...

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Work at BIOCON "A"

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...

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Job as Scientific Officer "A"

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...

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B.Pharm, M.Pharm candidates required at Chantilly BioPharma "A"

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...

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Opening for Clinical Scientific Expert-II at Novartis "A"

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...

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Hiring Drive : Clinical SAS Programmers in Bangalore 11th NOV 2016 "A"

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...

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Regulatory Affairs Biologics Job "A"

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...

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Medical Coding job at DELL "A"

 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...

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Jobs at Visionary RCM "A"

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,...

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Clinical Trial Associate required at Sun Pharma "A"

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...

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Drug Safety Physician(mbbs Fresher/md Pharmacology) "A"

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...

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Opening for Regulatory Writing/ Medical Writing at Indegene, Bangalore "A"

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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Business Executive_metabolics_cardio-diabetic at BIOCON "A"

Job Description To attain or exceed the targeted sales volume in the assigned territory. To develop relations with the selected doctors in the assigned territory. To implement HO strategies on the field.       Apply now...

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Excellent Opportunity to Work @ Novozymes "A"

Pioneer a brighter future At Novozymes, we work in close partnership with our customers to make an impact and help create a better world. For those around us, for each other and for the next generation. We use science to advance industries, and as part of R&D, you will create and develop the biological answers that will pave the way for a brighter future. Job Title : Research Associate, Regional Innovation, R&T, Bengaluru Are you...

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Freshers Job : Biocon "A"

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...

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Walk in interview at Sun Pharma "A"

Sun Pharma an international,specialty pharmaceutical company headquartered in India with a global manufacturing network across 25 countries. We manufacture and market a large basket of pharmaceutical formulations as branded generics & generics in India, US and across the world. Our leadership is approachable, encourages transparency & strong work ethics to ensure that people get the best opportunities to learn and grow. We encourage...

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Panacea Biotec Jobs "A"

Panacea Biotec is a leading research based Health Management Company, with an annual turnover of approx. Rs. 830 Crores. We are engaged in research, development, manufacture & marketing of Vaccines, Bio-Pharmaceuticals and Pharmaceuticals (Rx & OTC) of international quality and Health Services. All Panacea Biotec plants are accredited by international agencies and they follow current Good Manufacturing Practices, as per WHO guidelines.We...

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Career opportunity for Safety Associate II at inVentiv Health "A"

Job Description: - Process adverse event reports received from sites/reporters.- Perform QC review of completed individual and periodic safety reports.- Complete data entry including writing of adverse event narrative and provide preliminary assessment of event seriousness and expectedness/listedness as per applicable Reference Safety Information.- Generate adverse event queries, liaise with the medical reviewers/client to agree upon the queries,...

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Job for Senior Medical Writer in Novartis "A"

Job Description1.Write/edit regulatory documents (e.g. CSRs, DSURs, RMPs, contribute to CTD summaries).2.Participate in planning of analysis and data presentation to be used in study reports or summary documents.3.Act as a member of clinical trial teams following protocol finalization4.Act as documentation consultant in clinical trial teams to ensure compliance of documentation to internal company standards and external regulatory guidelines.5.Act...

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