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Friday 30 September 2016

Applications are invited from the eligible candidates for filling up the post of Two Posts of “Senior Research Fellow” and Two Posts of “Project Trainee” on contract basis for the DBT funded project – I entitled “A multi centric study to develop comprehensive molecular genetic panels for glioblastoma personalized therapy”
DBT Project –II entitled “ Unraveling genetic and epigenetic landscape of gliblastoma: Insights into the therapy resistance and recurrence “Programme support on molecular Neuro-Oncology (Phase II)”  under Dr. Vani Santosh, Professor & Head Department of Neuro Pathology & Principal Investigator.


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Apply now
The Advanced Centre for Treatment, Research and Education in Cancer (ACTREC) is the state-of-the-art R&D satellite of the Tata Memorial Centre (TMC), which also includes under its umbrella the Tata Memorial Hospital (TMH), the largest cancer hospital in Asia. ACTREC has the mandate to function as a national centre for treatment, research and education in cancer. TMC is an autonomous grant-in-aid institution of the Department of Atomic Energy (DAE), Government of India. It is registered under the Societies Registration Act (1860) and the Bombay Public Trust Act (1950). Its Governing Council is headed by the Chairman, Atomic Energy Commission, Government of India.


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Walk-In Details:
  • Date of Interview – 05th October 2016
  • Time of Interview – 02:00 PM
  • Venue of Interview – Meeting Room, 3rd floor, Khanolkar Shodhika, ACTREC
Malabar Cancer Centre is an autonomous institution under Health and Family Welfare Department, Government of Kerala registered under Societies Registration Act XXI of 1860, with an aim to establish a hospital, providing the much-required oncology care to the population of North Kerala. The main objective being establishing a modern Cancer Hospital and Research and Training Centre of international standard in treatment and prevention of cancer.
Applications are invited for the following posts:
Position 1
Name of the post: Lecturer in molecular oncology

Scale of pay – (Rs 15600- 39100, Grade pay: Rs 5,400)


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How to Apply :
Interested candidates may apply in the prescribed format and should submit printed application, with attested certificates copies (for proving age, qualification, experience etc.) along with D.D worth Rs.1000/- (Rupees thousand only) favoring Director, Malabar Cancer Centre, payable at Thalassery. Applications will be available from the website of MCC www.mcc.kerala.gov.in.

The last date of submission of application along with Demand Draft should be forwarded to The Director, Malabar Cancer Centre, Moozhikkara PO, Thalassery, Kerala-670103, on or before 20/10/2016 till 4.30 PM. Application form and details are available in http://www.mcc.kerala.gov.in 
Lupin Limited is one of India’s largest manufacturers of bulk actives and formulations. The principal bulk actives manufactured by it include Rifampicin, Pyrazinamide, Ethambutol (anti-TB), Cephalosporins (anti-infectives) and cardiovasculars. The company also possesses competencies in phytomedicines, in which medicines are made out of plant and herbal resources supported by the discipline of modern medicine.
Job Title : Officer – Quality Control


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The Nizam’s Institute of Medical Sciences shortly NIMS is an Institute under State Legislature Act in Hyderabad, Telangana, India. It is established under the Act of Andhra Pradesh State Legislature.It has campuses in Punjagutta and Bibinagar.
Job Title – Research Coordinator
No.of.Posts – ONE

Project Title – “A Randomized, Double-blind, Event-driven, Placebo-controlled, Multicentre Study of the Effects of Canagliflozen on Renal and Cardiovascular Outcomes in Subjects With Type 2 Diabetes Mellitus and Diabetic Nephropathy”

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How to Apply:
  • The applications should be submitted in the enclosed format (by copying on a plain paper) and must be accompanied by attested copies of certificates in support of all information furnished in the application.

Application Deadline – 03rd October 2016
Quintiles is the only fully integrated biopharmaceutical services company offering clinical, commercial, consulting and capital solutions worldwide. Our network of 23,000 engaged professionals in 60 countries around the globe works with an unwavering commitment to patients, safety and ethics — ensuring a higher level of healthcare for people. For our biopharmaceutical customers, we help them navigate risk and seize opportunities in an environment where change is constant.
Post: Pharmacovigilance

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Envision Scientific Pvt. Ltd. is a leading provider of drug delivery technologies to the healthcare industry. Our developed technologies are designed to be utilized for various types of drug and different delivery systems. Its proprietary NANO ACTIVETM Technology is designed for drug delivery utilizing Nanotechnology from various types of devices and surfaces. We Vision To have a Happy and Healthy World. Envision Scientific was incorporated in 2008. The company is ISO 9001:2008 and ISO 13485:2003 certified unit. The company was listed in the top 10 companies with IP fillings in the pharmaceutical sector for the year 2010 by the government of India gazette.
Post: Officer-production

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Job Description:
Responsible for General Maintenance of Equipment & Instruments involved.
Responsible for Drug Coating Of All Products.
Responsible to maintain the documents & records as per ISO.
Responsible for Primary packaging.
Responsible for sterilization of all products.
Responsible to maintain clean room condition and clean room garments availability.
Daily reporting to Sr. Executive/Executive Production.
Beside all the above responsibilities management reserves the right to give you any additional work as per requirement of organization


send your resume to hr@espl.net.in
RESPONSIBILITIES

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• Serve as Lead Programmer on the corporate team.
• Plan and coordinate database design, development, implementation, maintenance, and user support of clinical systems.
• Provide technical expertise in conjunction with internal and external clients.
• Program, test, and document databases in accordance with programming standards and validation procedures.
• Program database manipulation and transfers of data for internal and external clients.
• Mentor other team members and Lead Programmers in training and developing technical and/or database expertise.
• Independently bring project solutions to the CDP teams and the Clinical Data Programming department.
• May assist IT in developing and implementing new technologies.
• May assist IT in testing and evaluating new upgrades to technologies.
• May assist in developing, revising, and maintaining core operating procedures and working instructions.
• Meet objectives as assigned, and interact with the project team to organize timelines, responsibilities and deliverables.
• Develop and maintain good communications and working relationships with teams and external clients.




PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. They have helped over 800 clients to develop and launch some of the most important drugs and devices of our time-helping people live better and healthier lives everywhere in the world. Headquartered near Boston, Massachusetts, PAREXEL operates in more than 50 countries around the world.

Post : Quality Manager

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Job Description

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  • You will be responsible to ensure a complete and accurate Trial Master File through documentation quality and consistency across programs.
  • You will determine and review study specific TMF specifications to ensure quality and standardization is established per program and kept up to date as program/protocols progress.
  • You will assess impact of potential changes to TMF specifications prior to implementation and collaborating with CPM if modifications are necessary.
  • You will review audit reports and document metrics for trends and to ensure that program document management deliverables are on target.
  • You will serve as a point of contact for providing responses to regulatory authorities with regard to documentation management activities for audits, regulatory submission issues and product defense

Thursday 29 September 2016


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Eligibility criteria

6) Applicants should be studying in one of the following:

  • BS / BSc / BVSc / BPharm (II and III years only)
  • BE / BTech / BCA (II and III years only)
  • MS / MSc / MVSc / MPharm (I year only)
  • ME / MTech / MCA (I year only)
  • (5-year integrated) MS / MSc /MTech / MBBS (II, III, IV years only)
  • (dual degree) BTech + MTech (II/III/IV years only)
  • (dual degree) BE + MSc (II, III, IV years only)
  • (dual degree) BS + MS (II, III, IV years only)
  • Integrated PhD (I, II years only)
Academy means Indian Academy of Sciences, Bengaluru. Academies mean Indian Academy of Sciences (Bengaluru), Indian National Science Academy (New Delhi), and The National Academy of Sciences, India (Allahabad).

 Guide means a person from the list of scientists/faculty approved by the Academies as guides.

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Job Description


Responsibilities:

1. Testing of all RM and PM.
2. Analyze trends in quality complaints and take preventive and corrective action for the same
3. Implement Quality systems e.g. ISO 9001, HACCP, 5S, SGA etc.
4. Develop and implement testing SOPs
5. Vendor certification
6. Design and implement processes as part of external and internal safety,hygiene and certification specifications


Incumbent will report to AM-Quality for the plant and is expected to work in rotating shifts.

B.Tech/M.Tech in Food Technology mandatory


Senior Research Associate / Associate Scientist – Protein Science Post Vacant


Incorporated in the year 1994, Syngene International is one of India’s premier contract research and manufacturing organizations in providing customized service. Our services encompasses all across discovery chain: early stage discovery, process development, cGMP manufacturing and formulation development both in the small molecule and novel biologics area. Based in Bangalore, Karnataka, the Company is situated in a 90 acre Special Economic Zone with over 100000 sq. mt of built up facilities.

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Job Description

  1. Good knowledge and experience in Protein Purification (FPLC and related) and Characterization (SDS-PAGE, Western Blot, )
  2. Independently execute protein expression (Bacterial)/purification projects .

Applications on prescribed format as per annexure-A to this Notice are invited from the eligible candidates who are permanent residents of J&K State for filling up of the following posts at SKIMS Medical College-Hospital, Bemina, Srinagar, under the Jammu & Kashmir Special Recruitment Rules, 2015 notified vide SRO. 202 of 2015 dated. 30-06-2015:-
Post: Junior Pharmacist

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Johnson & Johnson is the world’s most comprehensive and broadly based manufacturer of health care products. The organization is comprised of more than 250 operating companies with over 128,000 employees located in some 60 countries. With Global sales of USD 71.3 billion in 2013, Johnson & Johnson is recognized as one of the most admired and respected companies in the world.
Post : Plant Quality Manager
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Job Description
Review and analysis of patients cardiac data
Interpretations of the data / ECG Reports.
Creation of a final test report.
Adherence to all company procedures and policies
Comfortable to work in Shifts


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Walk in at CHC Healthcare, 26 /1, East Patel Nagar,  Near Union bank and Axis Bank Delhi
send your email to hr@chcgroup.in
PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. They have helped over 800 clients to develop and launch some of the most important drugs and devices of our time-helping people live better and healthier lives everywhere in the world. Headquartered near Boston, Massachusetts, PAREXEL operates in more than 50 countries around the world.
Post: Clinical Research Associate II

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Ahlcon Parenterals (India) Ltd, an ambitious venture to manufacture life saving Intravenous Fluids and medical disposals by employing a highly sophisticated production process, the aseptic Blow-Fill-Seal Technology imported from Europe and U.S. . Ahlcon has an installed capacity of 30 million bottles per annum for LVP in pack size of 100ml, 200ml, 300ml and 500ml packs. The company also has capacity of 150 million vials of Eye drops and Injections in the fill size of 2ml, 3ml, 5ml, 10ml and 20ml both in transparent and white opaque packs as SVP.


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Walk in 
Date 01/10/2016(Saturday)
Timings : 10Am to 5:30 PM
Venue : Hotel K.C CROSS ROAD Sec-10 Panchkula, Haryana
Job Description
The principal responsibility of the Research Scientist is the analysis by multiple procedures of intermediates and target compounds.  The Research Scientist is expected to demonstrate expertise in both the theoretical and practical aspects of analytical chemistry.  A major component in the scientist's performance rating will be based on productivity. In general, technical, organizational and compliance support for 170+ ongoing stability studies.



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Apply here

Wednesday 28 September 2016

NATURE OF SUPPORT
  • The amount of the fellowship is Rs. 25,000/- per month in addition to regular salary
    from the host institute. If an awardee is receiving salary from international organization,
    he will be entitled for research grant i.e. contingency only.
  • In addition, each Fellow will receive a contingency grant of Rs. 6.00 lakh per annum
    for meeting the expenses on consumables, equipment, international and domestic
    travel, manpower and other contingent expenditure to be incurred in connection with
    the implementation of ongoing research project under the fellowship.
  • The Tata Innovation Fellows would be eligible for other regular research grant(s)
    through extramural and other research schemes of various S&T agencies of the
    Government of India.
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HOST INSTITUTION

  • The candidate will continue to work at the place of his/her employment.
  • The Institution where the candidate is working would provide the necessary
    infrastructure and administrative support for pursuing the research under this
    fellowship.

HOW TO APPLY:
Application (six copies) may be sent as per proforma downloadable from DBT website
(www.dbtindia.nic.in) and duly forwarded by the competent authority to Dr. A. K. Rawat,
Scientist ‘F’, Department of Biotechnology, Block-2, CGO Complex, Lodhi Road,
New Delhi -110 003, latest by 21st November, 2016.

Long Description
Job Accountabilities
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  1. Setup the cultivation practise to develop inoculum from lab to open ponds
  2. Develop the protocol for inoculum scale up
  3. Carry out nutrient management studies in bench scale to develop protocol.
  4. Validate the control management in bench scale for developing good cultivation practise
  5. Coordination with operation team in developing SOP for pond operation..
  6. Study the stain adaptation and growth optimization on non-season to develop inoculum for production ponds

Skills Required (Knowledge and Skills)

Knowledge : The candidate should have a good understanding in Algae cultivation or Cell culture in bioreactors.



Job Description 
  • Validate Bioanalytical method in biological matrix.
  • Analyze biological samples of allotted projects.
  • Handling and the operations of LC-MS/MS.
  • Calibration of Bioanalytical instruments.
  • Ensure effective implementation of GLP and 21 CFR Guidelines

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The Indian Institute of Technology Kharagpur (IIT Kharagpur or IIT KGP) is a public engineering institution established by the government of India in 1951. It was the first of the IITs to be established, and is recognized as an Institute of National Importance by the government of India.
As part of Nehru’s dream for a free self-sufficient India, the institute was established to train scientists and engineers after India attained independence in 1947. It shares its organisational structure and undergraduate admission process with sister IITs. The students and alumni of IIT Kharagpur are informally referred to as KGPians. Among all IITs, IIT Kharagpur has the largest campus (2,100 acres), the most departments, and the highest student enrollment. IIT Kharagpur is known for its festivals: Spring Fest (Social and Cultural Festival) and Kshitij (Asia’s largest Techno-Management Festival).


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Applications are invited for the following temporary post in the research project under Prof. T. Velpandian
Post : SRF - 01 post


Please submit your CV latest by 5th Oct 2016 in Room No. 635, 6th Floor, Ocular Pharmacology & Pharmacy Division, Dr. R.P. Centre for Ophthalmic Sciences, AIIMS, New Delhi. Or send by email oculpharm@gmail.com
Only shortlisted candidates will be invited for interview.
No. TA/DA will be given for attending the interview.
Note:- Applications are invited from Delhi and NCR only.



Job Description :
A. Primary Research/ Secondary research on Pharma companies, their drugs, sale.
B. Data mining & data uploading.
C. To collect information regarding pharmaceutical companies & their annual product sales.
D. To promote pharma companies for their Business Development.
E. To write pharmaceutical articles that is published


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Interested candidates can apply to below mentioned e-mail Id:- praveen@alchemphytoceuticals.com
Job PURPOSE  
Good communication skills
Good interpersonal skills and good attitude
Good knowledge in Pharmacovigilance(case processing and drug safety)


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If interested kindly send your updated resume to my email id- roshini.y@quintiles.com
ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies
ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.
Post: Clinical Trial Assistant

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Responsibilities  
The incumbent will be responsible for leading a team of scientists engaged in conducting formulation research and development activities on generic molecules, reformulation of existing drug products for life cycle management and new chemical entities. The area of formulation research includes solid and liquid dosage forms for oral, topical and parenteral administration to animals. The scope of research activities would typically include pre-formulation, prototype formulation and scale up studies as part of product development and subsequently the transfer of processes and technologies to commercial manufacturing sites. The position will involve developing and executing technical plans to meet target drug product profiles through in house research as well as external collaborations. The incumbent will be expected to ensure effective collaboration with various stake holders and customer groups such as global development team, regulatory, quality, manufacturing, marketing and clinical organizations for successful and timely delivery of clinical supplies and manufacturing process transfers. Other than the research activities the candidate will also be responsible for maintaining and delivering required documentation such as protocols, reports, SOPs, CMC technical sections for regulatory submission etc. Effective communication skills, leadership skills and people development skills are essential. The position would involve managing direct reports and travel up to about 25% of time.


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Topping the list of the Asian pharma elite is India's Dilip Shanghvi, who founded Sun Pharmaceuticals along with partner Pradeep Ghosh in 1982. The company's acquisitions of Caraco Pharma, Taro Pharma and, more recently, fellow Indian company Ranbaxy Laboratories have made Sun Pharma into India's largest drugmaker.
Shanghvi stepped down as chairman and CEO of the company in 2012, but he remains managing director, as well as chairman of Sun Pharmaceutical Advanced Research, which is spearheading the group's push into proprietary medicines. His $16.7 billion fortune ranks him at number 44 in the overall Forbes list.
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In second position among Asia's pharma rich is Cyrus Poonawalla, chairman of the Poonawalla Group, which includes Serum Institute of India, India's largest biotech company, which specializes in manufacturing pediatric vaccines.

Poonawalla set up Serum Institute of India in 1966, at a time when lifesaving vaccines were in short supply in India, and those were imported at high prices. The company has since grown to become the world's largest vaccine producer in terms of the number of doses produced and sold globally. With a net worth of $8.5 billion, Poonawalla sits at position 133 in the Forbes list.

source:http://www.fiercepharma.com/pharma-asia/sun-pharma-s-dilip-shanghvi-heads-list-top-asian-pharma-billionaires

Tuesday 27 September 2016

CDFD, an autonomous institute of the Department of Biotechnology, Ministry of Science and Technology, invites applications from Indian nationals for the following purely temporary vacancies in research projects funded by National / International agencies at CDFD like DST/DBT/ICMR/CSIR etc. The description of the positions and minimum qualifications for various vacancies are as follows:
Position 1
Job Title : Research Associate


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Job Title : Junior Research Fellow/ Project Assistant /Research Assistant


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Central Warehousing Corporation, a Schedule-A Mini-Ratna, Category-I, Central Public Sector Undertaking under the administrative control of Ministry of Consumer Affairs, Food & Public Distribution, providing Scientific storage facilities for agricultural inputs, produce and other notified commodities besides providing logistics infrastructure like CFSs/ICDs, Land Custom Stations, Air Cargo Complexes etc. for import-export cargo, invites online application from eligible candidates, who fulfil the prescribed qualification, experience, age, etc., for the posts indicated below:

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Position 1
Job Title:  Management Trainee (Technical)
Number of Vacancies: Six

Eligibility:  1st class Post Graduate degree in Agriculture with Entomology or Microbiology or Bio-chemistry OR 1st class Post Graduate degree in Bio-Chemistry OR Zoology with Entomology from recognized University/ Institution. Preference will be given to those who also possess Post Graduate Diploma in Warehousing and Cold chain Management/ Quality Management.

How To Apply: 
Candidates can apply online only from 20.09.2016 to 13.10.2016 and no other mode of application will be accepted.

2016-09-25_13-57-21 multiple openings @ central warehousing corporation

Job Description

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    Walk-in Life Science Freshers for Medical Coding @ Vee Technologies

    Current Requirement : Medical Coder Trainee

    Eligibility : Freshers (Life Science Graduates) + Ready to work in Night Shift

    Work Location : Bangalore & Chennai
    Date: Sep 27th - 30th

Job Description


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    Responsibilities/Authorities : 

    1.Prioritise Data Entry activities for Cases by reference to the Date Receipt in accordance with SOPs and Guidelines;
    2.Data entry of safety information, including relevant medical history and laboratory data and therapy dates into the applicable Global Safety Database in accordance with Guidelines and SOPs;
    3.Validate data consistency and make any corrections as needed;
    Submit to Case Safety Reports for scientific and medical evaluation;
    4.Review responses to queries when received and update the Global Safety Database as required;
    5.Document any amendments to the Data Entry Conventions and agree these with the client Functional Lead, prior to their implementation;
    6.Participate in clinical study reconciliation activities, as requested by client; and
    7.Issue reconciliation listings as requested by client to the relevant Connected Entity and to client.

    Requirements 

    Fresher's also can apply with B.pharma/M.pharma/BDS/Pharma D from 2014,2015,2016 passed out.
    Healthcare degree preferred;
    For Experienced: 

    A minimum of 2 years Pharmaceutical or Clinical experience is preferred;
    1.Experience with MS Office products;
    Knowledge of coding applications, databases, processes and tools is preferred;
    2.Experience in researching information utilizing available resources including publications and the World Wide Web;
    3.Effective communication, organisation and time management skills;
    4.Good interpersonal skills and the ability to operate effectively in an international environment;
    5.English language (written) proficiency must.
    6.Thorough knowledge of medical terminology;
    7.Computer proficiency and ability to work in specific databases;
    8.Excellent written and verbal communication skills is a must
    NOTE :
    Candidates from Bangalore preferred.
    candidates should be flexible to work in shifts.

    Apply now

Job Description

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    Dear All,

    We are pleased to inform you that we have multiple positions opened for Pharmacovigilance.

    Experience - 2 to 8 years
    Skills Required - Case Processing
    Job Location - Bangalore
    Date & Time - 1st October 2016

Job Description

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    SRF Animal Biotechnology Job Position in Anand Agricultural University

    Project Title : "Evaluation of in-vitro and in-vivo efficacy of a formulation containing nanotechnology based alkyl polyglycosides of herbs against mastitis pathogens and its post-exposure effect on gene expression of certain bacteria" (B.H. 18457-62)
    Apply here

Job Description


This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. As a TMF Specialist you will complete Document Management activities in support of client services contracts and internal ICON business needs.

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Overview of the role
Process study documents in accordance with client and study requirements as per study-specific processes, ICON SOPs/WPs and regulations, where applicable.
Liaise with study teams and other Document Management staff in order to fulfill job responsibilities and activities.
Complete departmental projects as assigned in accordance with specified timelines, ICON SOPs/WPs and regulations.
Maintain study files as per study and/or client requirements or in accordance with ICON SOPs/WPs and applicable regulations.
Complete activities related to document receipt and processing which may include but is not limited to: document receipt and review, scanning and indexing, quality control, copying, filing, forwarding or return to client/study teams and archiving.
Provide information necessary to complete client and/or departmental status reports as requested by the management of the Document Management department.

Monday 26 September 2016

Central Medical Services Society, a Central Procurement Agency under Department of Health & Family Welfare, has been set up registered under Societies Registration Act, XXI of 1860 to procure and distribute health sector goods to the State Governments. The Society is looking for following warehouse staff at each of 13 locations:
Post: Pharmacist

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Who can Apply:
Pharmacists  employed with state Governments in the same scale or in PB-1, Rs 5200-200-20200, Grade pay Rs 2800 with 5 years of service     Or  
Individuals meeting age, education and experience criterion as mentioned at Sr no7 & 8 may apply directly for recruitment on contract basis.




A new study of classical Chinese medical texts identifies references to age-related memory impairment similar to modern-day Alzheimer's disease, and to several plant-based ingredients used centuries ago -- and still in use today -- to treat memory impairment. Experimental studies of five of these traditional Chinese medicines suggest that they have biological activity relevant to Alzheimer's disease, according to an article in The Journal of Alternative and Complementary Medicine, a peer-reviewed publication from Mary Ann Liebert, Inc.
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Charlie Xue, PhD and coauthors from Guangdong Provincial Academy of Chinese Medical Sciences and Guangdong Provincial Hospital of Chinese Medicine, China, and RMIT University, Australia, performed a comprehensive, systematic search of the Encyclopedia of Traditional Chinese Medicine, a database of more than 1,000 Chinese medical books dating back to the fourth century.
In the article "Memory Impairment, Dementia and Alzheimer's Disease in Classical and Contemporary Traditional Chinese Medicine the authors describe specific mentions of signs and symptoms of memory impairment associated with aging and the formulas and ingredients most commonly used to treat these disorders.








DRDO, India’s premier R&D organization employs bright, qualified and competent scientists in Group ‘A’ (Gazetted) technical service known as Defence Research & Development Service (DRDS). DRDO offers exciting and challenging career opportunities in very broad spectrum of R&D at its more than 50 laboratories/establishments throughout the country. For further information about DRDO please visit DRDO website.
Recruitment & Assessment Centre (RAC) Invites online Recruitment Applications through RAC website rac.gov.in  for the post of Scientist 'B' in DRDO.

Post: Scientist 'B' (Chemistry & Pharmacy)

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How to Apply:
Online registration on RAC website rac.gov.in/) is mandatory.
i) Candidates are required to submit their applications online alongwith legible and lighter file containing scanned copies of certificates for essential and higher educational qualification, if any, alongwith percentage of marks (duly supported by the mark-sheets), date of birth certificate, experience claimed if any in the column pertaining to employment history of online application, a recent passport size colour photograph (size not exceeding 30 KB; resolution of 110 x 140 pixels) and the details of required application fees through RAC website. The maximum file size of each attachment should not exceed 500 KB and it must be legible when a printout is taken.
ii) All candidates, whether in Govt. service or in Govt. owned organisations, should also submit their applications online directly to the Recruitment and Assessment Centre (RAC) and such candidates are required to upload a signed declaration (as per the proforma available at RAC website) that they have informed their Cadre Controlling Authority (CCA) in writing, that they have applied for the post in DRDO. However, such candidates, if in regular service whether in permanent or temporary capacity, are required to produce a “No Objection Certificate”(NOC) from their CCA as per the proforma available at RAC  website at the time of interview, in addition to the aforesaid declaration. If CCA considers withholding the NOC, the candidate should inform RAC within 30 days of the closing date.
iii) Candidates are advised to retain a copy of the online recruitment application (pdf) alongwith acknowledge slip generated after locking of online application form.
iv) Application completed in all respect will only be considered as locked application and only such applications shall be considered for further processing.
A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.
PostSenior Clinical Manager

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Apply now
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