Is it true that barc recruits biological student through gate exam??
BARC recruits biological students through GATE exam?
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Gate previous year papers
Respected sir,
I wish to know whether gate previous year questions repeat in gate exams.
I wish to know whether gate previous year questions repeat in gate exams.
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Multiple Job Opportunities at Syngene International Limited , Bangalore
Recruitment Drive for Drug Metabolism Pharmacokinetics ( DMPK ) on 16 September 2017, Saturday @ Bangalore.
Date : 16th September 2017
Time : 9.00 A.M
Venue : Syngene International , Biocon Park , PLOT 2 & 3, Biommasandra Phase IV , Jigani Link Road , Bangalore - 99
Designation : Sr. Research Scientist / Research Scientist / Sr. Associate Scientist / Associate Scientist.
Open Positions : 4
Experience : 5 - 8 years
Qualification : MSc ( Biochemistry / Biological Sciences ) M Pharma from a reputed University.
Roles and Responsibilities :
1. Perform in vitro ADME assays such as solubility , metabolic stability , CYP450 inhibition , plasma protein binding , TDI , IC - 50 shift etc.
2. Processing of plasma and tissue samples from bioanalysis.
3. Operating Instruments like LC - MS / MS for compound tuning and analysis , followed by data retrieval , method development of NCEs in plasma and other matrices.
4. Analytical problem solving skills.
5. Knowledge on TOF based application.
6. Hands on TOF operation is preferable.
Candidate's Desired Profile :
1. Excellent interpersonal and communication skills ( written and spoken ).
2. Candidate should have strong commitment to team work as well as high levels of integrity , professionalism and personal ethics.
Designation : Principal Scientist
Open Positions : 1
Experience : Essential : PhD with with 6 - 8 years experience in DMPK in a R&D set up.
Note : If No PhD then MSc / M. Pharma with 8 - 10 years of experience in DMPK Science in a reputed Drug discovery company is acceptable.
Mandatory : Candidate has to prepare a brief slide deck on related to their scientific work / interest. It can be discussed on the case study of Drug discovery from the literature.
Roles and Responsibilities :
1. Hands on experience in conducting various in vitro studies to assess the ADME of discovery compounds ( cell culture , metabolic stability models , CYP inhibition , protein binding etc. ) required.
2. A thorough understanding of bioanalysis of using LC - MS / MS is required.
3. Prior experience in handling data using software/s is required.
4. Strong problem solving , leadership and mentoring skills are required.
5. Lead a team in the DMPK department , focused on non-clinical evaluation of new chemical entities in various in vitro ADME assays in support of various drug discovery programs ranging from early to late stage discovery.
Required Documents : Copy of Resume , 2 months pay slips , Salary breakup and 1 passport size photograph.
Date : 16th September 2017
Time : 9.00 A.M
Venue : Syngene International , Biocon Park , PLOT 2 & 3, Biommasandra Phase IV , Jigani Link Road , Bangalore - 99
Designation : Sr. Research Scientist / Research Scientist / Sr. Associate Scientist / Associate Scientist.
Open Positions : 4
Experience : 5 - 8 years
Qualification : MSc ( Biochemistry / Biological Sciences ) M Pharma from a reputed University.
Roles and Responsibilities :
1. Perform in vitro ADME assays such as solubility , metabolic stability , CYP450 inhibition , plasma protein binding , TDI , IC - 50 shift etc.
2. Processing of plasma and tissue samples from bioanalysis.
3. Operating Instruments like LC - MS / MS for compound tuning and analysis , followed by data retrieval , method development of NCEs in plasma and other matrices.
4. Analytical problem solving skills.
5. Knowledge on TOF based application.
6. Hands on TOF operation is preferable.
Candidate's Desired Profile :
1. Excellent interpersonal and communication skills ( written and spoken ).
2. Candidate should have strong commitment to team work as well as high levels of integrity , professionalism and personal ethics.
Designation : Principal Scientist
Open Positions : 1
Experience : Essential : PhD with with 6 - 8 years experience in DMPK in a R&D set up.
Note : If No PhD then MSc / M. Pharma with 8 - 10 years of experience in DMPK Science in a reputed Drug discovery company is acceptable.
Mandatory : Candidate has to prepare a brief slide deck on related to their scientific work / interest. It can be discussed on the case study of Drug discovery from the literature.
Roles and Responsibilities :
1. Hands on experience in conducting various in vitro studies to assess the ADME of discovery compounds ( cell culture , metabolic stability models , CYP inhibition , protein binding etc. ) required.
2. A thorough understanding of bioanalysis of using LC - MS / MS is required.
3. Prior experience in handling data using software/s is required.
4. Strong problem solving , leadership and mentoring skills are required.
5. Lead a team in the DMPK department , focused on non-clinical evaluation of new chemical entities in various in vitro ADME assays in support of various drug discovery programs ranging from early to late stage discovery.
Required Documents : Copy of Resume , 2 months pay slips , Salary breakup and 1 passport size photograph.
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Job Opportunities at Premas Biotech, Manesar ,Gurgaon , India
Designation : Senior Research Scientist - Downstream Process Development.
Position code : ( SRS - DSP)
Positions : 2
Experience : MSc or PhD with 4 - 7 years of significant exposure to process development, and delivery of therapeutic proteins. Consistent track record of deliveries will be important.
Designation : Manufacturing Officer -
Downstream Processing
Position code : ( MO - DSP )
Positions : 1
Experience : B.Tech / MSc with 7 - 10 years of significant exposure and delivery of therapeutic proteins. Consistent track record of deliveries will be important.
Designation : Interns - Downstream Processing
Position code : ( I - DSP )
Positions : 2
Experience : Fresh B.Tech / MSc with interest to learn and contribute to the world of therapeutic proteins. Should have accomplished one unique contribution to their immediate society ( teaching underprivileged children, etc) or learnt a language or acquired an unique skill.
Rush your resume to careers @ premasbiotech.com with the position code.
Position code : ( SRS - DSP)
Positions : 2
Experience : MSc or PhD with 4 - 7 years of significant exposure to process development, and delivery of therapeutic proteins. Consistent track record of deliveries will be important.
Designation : Manufacturing Officer -
Downstream Processing
Position code : ( MO - DSP )
Positions : 1
Experience : B.Tech / MSc with 7 - 10 years of significant exposure and delivery of therapeutic proteins. Consistent track record of deliveries will be important.
Designation : Interns - Downstream Processing
Position code : ( I - DSP )
Positions : 2
Experience : Fresh B.Tech / MSc with interest to learn and contribute to the world of therapeutic proteins. Should have accomplished one unique contribution to their immediate society ( teaching underprivileged children, etc) or learnt a language or acquired an unique skill.
Rush your resume to careers @ premasbiotech.com with the position code.
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Campus Recruitment Drive by Hetero Biopharma at Andhra University,Visakhapatnam
Pooled Campus Drive for freshers from Life Sciences Stream
Date : 14th September 2017 , Thursday
Time : 9.00 AM to 3.00 PM
Venue : Andhra University Campus , Visakhapatnam , Andhra Pradesh
Division : Hetero Biopharma Ltd.
Work location : Jadcherla, Mahbubnagar ,Telangana
Department : R&D, Manufacturing , Quality Control
Designation : Junior Officers, Junior Research Associates
Required qualification pool : ( 2015 ,2016 and 2017 passouts ) B.Tech / M.Tech from Biotech / Biochemical engg. , M.Sc. From Biotechnology , Biochemistry and Microbiology.
Please Refer this ad for further details :
Date : 14th September 2017 , Thursday
Time : 9.00 AM to 3.00 PM
Venue : Andhra University Campus , Visakhapatnam , Andhra Pradesh
Division : Hetero Biopharma Ltd.
Work location : Jadcherla, Mahbubnagar ,Telangana
Department : R&D, Manufacturing , Quality Control
Designation : Junior Officers, Junior Research Associates
Required qualification pool : ( 2015 ,2016 and 2017 passouts ) B.Tech / M.Tech from Biotech / Biochemical engg. , M.Sc. From Biotechnology , Biochemistry and Microbiology.
Please Refer this ad for further details :
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Multiple Job opportunities at Premas Biotech, Gurgaon,India
Designation : Manager - Analytical Development
Positions : 1 ( MGR - AD )
Experience : MSc or PhD with 7 - 10 years of significant exposure to Analytical method development to MAbs, therapeutic proteins, biophysical characterisation , and comprehensive understanding of proteins. Leading from the front along with hands on approach is a critical criteria.
Designation : Senior Research Scientist - Bio-analytical Development
Positions : 1 ( SRS - BLD )
Experience : MSc or PhD with 4 - 7 years of significant exposure to Analytical method development to MAbs, therapeutic proteins. Understanding higher structure and analytics will be critical for the position.
Designation : Manager - Upstream Process Development
Positions : 1 ( MGR - USP )
Experience : MSc or PhD with 7 - 10 years of significant exposure to process development , microbial , mammalian , up to 2 - 50 L , media development and delivery of therapeutic proteins.Leading from the front along with hands on approach is a critical criteria.
Designation : Senior Research Scientist - Upstream Process development - Mammalian
Positions - 1 ( SRS - USP )
Experience : MSc or PhD with 4 - 7 years of significant exposure to Upstream Process Development , bioreactors ( 1-20 L ) , media development and delivery of MAbs. Consistent track record of deliveries will be important.
Designation : Interns - Fermentation
Position code : ( I - USP )
Positions : 2
Experience : Fresh B.Tech / MSc with interest to learn and contribute to the world of therapeutic proteins. Should have accomplished one unique contribution to their immediate society ( teaching underprivileged children, etc) or learnt a language or acquired an unique skill.
Rush your resume to careers @ premasbiotech.com with the position code.
Positions : 1 ( MGR - AD )
Experience : MSc or PhD with 7 - 10 years of significant exposure to Analytical method development to MAbs, therapeutic proteins, biophysical characterisation , and comprehensive understanding of proteins. Leading from the front along with hands on approach is a critical criteria.
Designation : Senior Research Scientist - Bio-analytical Development
Positions : 1 ( SRS - BLD )
Experience : MSc or PhD with 4 - 7 years of significant exposure to Analytical method development to MAbs, therapeutic proteins. Understanding higher structure and analytics will be critical for the position.
Designation : Manager - Upstream Process Development
Positions : 1 ( MGR - USP )
Experience : MSc or PhD with 7 - 10 years of significant exposure to process development , microbial , mammalian , up to 2 - 50 L , media development and delivery of therapeutic proteins.Leading from the front along with hands on approach is a critical criteria.
Designation : Senior Research Scientist - Upstream Process development - Mammalian
Positions - 1 ( SRS - USP )
Experience : MSc or PhD with 4 - 7 years of significant exposure to Upstream Process Development , bioreactors ( 1-20 L ) , media development and delivery of MAbs. Consistent track record of deliveries will be important.
Designation : Interns - Fermentation
Position code : ( I - USP )
Positions : 2
Experience : Fresh B.Tech / MSc with interest to learn and contribute to the world of therapeutic proteins. Should have accomplished one unique contribution to their immediate society ( teaching underprivileged children, etc) or learnt a language or acquired an unique skill.
Rush your resume to careers @ premasbiotech.com with the position code.
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Microbiota succession on soil
Propose a schematic presentation of possible microbiota succession on decomposition of plant residues on acidic soil surfaces
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Clinical SAS career opportunities
Dear sir, I hv completed my btech in biotechnology and would like to know, what are the career opportunities in clinical SAS and what courses and exams should I do to achieve success in this field
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Job Opportunity at Hetero Biopharma,jadcherla, Mahabubnagar, Telangana
Walk - Interview for Freshers
Venue details :
Hetero coroporate,
# 7 - 2 - A2 , Industrial Estate ,
Sanath nagar , Hyedrabad.
Date :
17th September , 2017 ( Sunday )
Timings : 9.30 AM - 3 PM
Department :
R&D , Manufacturing , QC
Educational Qualifications :
M.Tech / B.Tech (Biotech) and
MSc ( Biotech or Biochemistry or Microbiology ).
Eligibility :
One should be a pass out of 2015 , 2016 & 2017 only with excellent academics and communication skills. Preferably Male Candidates are require.
Job Location : Jadcherla , Mahabubnagar , Telangana.
Candidates need to carry a photograph with all educational documents.
[u] Note : Candidates those who cannot attend this walk in, can share their CV's to [email]vinaykumar.b@heterodrugs.com
[/email]
Venue details :
Hetero coroporate,
# 7 - 2 - A2 , Industrial Estate ,
Sanath nagar , Hyedrabad.
Date :
17th September , 2017 ( Sunday )
Timings : 9.30 AM - 3 PM
Department :
R&D , Manufacturing , QC
Educational Qualifications :
M.Tech / B.Tech (Biotech) and
MSc ( Biotech or Biochemistry or Microbiology ).
Eligibility :
One should be a pass out of 2015 , 2016 & 2017 only with excellent academics and communication skills. Preferably Male Candidates are require.
Job Location : Jadcherla , Mahabubnagar , Telangana.
Candidates need to carry a photograph with all educational documents.
[u] Note : Candidates those who cannot attend this walk in, can share their CV's to [email]vinaykumar.b@heterodrugs.com
[/email]
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Job Opportunity at Strand , Bangalore , India
Designation : Technical Support Engineer
Full Time | Bangalore | Freshers may apply
Educational Qualification :
M.Tech / MSc in any Life Sciences with
- Excellent communication skills.
- Willing to work in shifts.
- Life Sciences Background
Job Description :
Would be providing technical support , advice and assistance to users on the range of products and services. Includes installations of the software and troubleshooting installations of on Windows , Mac and Linux platforms. As the clientele is global , candidates are required to work in shifts. Shifts may be day shifts , noon shifts , evening shifts and night shifts.
Salary : Upto 3 Lakhs
Send in your resumes to tech@biohiring.com with Job Title as Subject
Full Time | Bangalore | Freshers may apply
Educational Qualification :
M.Tech / MSc in any Life Sciences with
- Excellent communication skills.
- Willing to work in shifts.
- Life Sciences Background
Job Description :
Would be providing technical support , advice and assistance to users on the range of products and services. Includes installations of the software and troubleshooting installations of on Windows , Mac and Linux platforms. As the clientele is global , candidates are required to work in shifts. Shifts may be day shifts , noon shifts , evening shifts and night shifts.
Salary : Upto 3 Lakhs
Send in your resumes to tech@biohiring.com with Job Title as Subject
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Job Opportunities at Vimta labs Ltd. Hyedrabad
Division : Biopharma
Designation :
Scientist
Desired Qualification & Experience
2 - 5 years
Job Description :
Experience in characterization of proteins using cell based assays and analytical methodologyMust have experience in assay development and validationExperience in handling instruments such as HPLC, ELISA Reader, qPCR, MALDI-TOF, etc is desirable
Location : Hyedrabad
Department : Biopharma
Designation :
Group Leader
Desired Qualification & Experience
M.Pharm/M.Tech/M.Sc in Biotechnology & 8-9 years
Job Description :
Experience in instruments like HPLC/ELISAReader/QPCR/CE/MALDI-TOF/ESI-MSExperience in core projects / assignments like Immunogenicity/PKMethod Development & Validation of Preclinical & ClinicalSamples for Proteins & mAbsExperience in Physiochemical & Cell Based Bioassays for mAbs & Proteins
Department : Biopharma
Division : Pre - Clinical
Designation :
Research Associate/Sr. Research Associate/Scientist/Sr. Scientist - Animal House
Desired Qualification & Experience :
M. V. Sc / B. V. Sc (Veterinary & AH) & 0-12 years of experience in toxicology.
Job Description :
Primary Responsibilities:
Animal House VeterinarianResponsible for day to day functioning of Animal Facility and Breeding of laboratory animalsFollow proper quarantine procedure to ensure release of good quality animals into the experiment areaEnsure proper veterinary care for research animals including rodents, rabbits, Guinea pigs and dogs consistent with guidelines established by the CPCSEA, AAALAC requirementsProvide and maintain high quality clinical health care and record keeping for all laboratory activities and support team investigators conduct and surgical proceduresEnsure proper waste management and disposal system as per the requirements of the local pollution boardInteraction with the Purchase, Analytical, Facility in-charge and QA to ensure proper upkeep of the Animal HousePlan and supply appropriate animals for testing by putting in place a proper animal procurement, breeding and holding programs so as to facilitate uninterrupted supply of animals to various groups in pre-clinical divisionIdentity and create effective networking for procurement of animals and other resources needed for day -to-day management of the Animal HouseUp -to-date maintenance of all documents pertaining to CPCSEA forms, quarantine, health checkups, maintenance, procurement of animals, feed, water and bedding material analysis data and inventory, accessories, breeding, supply, euthanasia, disposal of animals and animal house materialsProactive preparation and planning of audits from internal or external QA, sponsors, regulatory authorities, certification authorities and TFF. Provide effective mechanisms for effective furnishing of related data to facilitate proper scrutinyAs a study veterinarian will be responsible for the welfare of the animals during conduct of the study and ensure that undue pain is not inflicted to the animals by the experimenterTo review or prepare all Animal House related SOPsResponsible for maintenance of training records of all animal housePlanning of activities during weekly offs and holidays in advancePreparation of healthy status report on animal inventoryPreparation of animal report for AAALAC submission
Secondary Responsibilities:
Monitor compliance of quality procedures and appropriate corrective actions to be taken on issuesTo train technical staff in animal handling and other animal husbandry activitiesUndertake internal quality audits and take corrective action to rectify deficienciesCoordinating with Purchase department for timely deliveries
Designation :
Research Associate/Sr. Research Associate/Scientist/Sr. Scientist/Group Leader - Genotoxicology
Desired Qualification & Experience :
M. Pharmacy Pharmacology / M. Sc Microbiology / M. Sc Toxicology & 1 – 13 Years
Job Description :
1. Study Director / Study Coordinator for In Vitro and In Vivo Genotoxicology studies
2. Validation of Core battery studies in Genetic Toxicology in accordance with OECD GLP norms
3. To monitor all aspects of studies and be an effective link between the testing facility and sponsor and coordinate from initiation of client discussion till termination of the project as a project manager
4. Experimental trial designing, conducting, coordinating and supervising the In Vitro and In Vivo Genotoxicology studies for various test substances using different test system/cell lines
5. Preparation, review and approval of protocols, progress reports, summary, interim reports, and detailed schedules for the In Vitro and In Vivo Genotoxicology studies. Maintenance and propagation of various established cell lines as per GLP compliance for Genetic toxicology studies
6. Maintenance and sub culturing of various bacterial tester strains for Bacterial Reverse Mutation Assay
7. Train Study Personnel in Proof of Concept (POC) animal models and GLP related documentation and report preparation
8. Plan, perform, conduct and monitor the core batteries of Genotoxicology studies
9. Coordinating with the in-vitro Toxicology team in standardization and new method validation of cytotoxicity assays
10. Communication with Management and sponsors related to the study issues.
11. Preparation of Study proposal (quotation), Study plan, Standard operating procedures and Study status to sponsor’s
12. To lead a team of people, weekly and monthly teamwork report preparation and submit to the HOD and Management
13. Overall responsibility for the planning, performing, reporting and archiving of the study
14. Ensure equipment qualification of instruments used in Genotoxicology and prepare user specification for Genotoxicology instruments and equipment to be procured for the department
15. Ensure all equipment and instruments are maintained in calibrated status. Monitor and maintain the equipment’s and instruments used in laboratory to avoid misuse and ensure minimum downtime for instruments by preventive maintenance Programme.
16. Check the studies for the Compliance to the regulatory requirements
17. Coordinating with QA during the facility audits and study based inspections
Location : Hyedrabad
Designation :
Sr. Research Associate/Scientist/Sr. Scientist/Group Leader/Deputy Manager – Genetic Toxicology In Vitro Lab
Desired Qualification & Experience :
M. Pharmacy Pharmacology / M. Sc Microbiology / M. Sc Toxicology & 3 – 12 Years
Job Description :
1. Study Director / Study Coordinator for In Vitro and In Vivo Genotoxicology studies.
2. Validation of Core battery studies in Genetic Toxicology in accordance with OECD GLP norms.
3. To monitor all aspects of studies and be an effective link between the testing facility and sponsor and coordinate from initiation of client discussion till termination of the project as a project manager.
4.Experimental trial designing, conducting, coordinating and supervising the In Vitro and In Vivo Genotoxicology studies for various test substances using different test system/cell lines.
5. Preparation, review and approval of protocols, progress reports, summary, interim reports, and detailed schedules for the In Vitroand In Vivo Genotoxicologystudies. Maintenance and propagation of various established cell lines as per GLP compliance for Genetic toxicology studies.
6. Maintenance and sub culturing of various bacterial tester strains for Bacterial Reverse Mutation Assay.
7. Train Study Personnel in Proof of Concept (POC) animal models and GLP related documentation and report preparation.
8. Plan, perform, conduct and monitor the core batteries of Genotoxicology studies.
9. Coordinating with the in-vitro Toxicology team in standardization and new method validation of cytotoxicity assays.
10. Communication with Management and sponsors related to the study issues.
11. Preparation of Study proposal (quotation), Study plan, Standard operating procedures and Study status to sponsor’s.
12. To lead a team of people, weekly and monthly teamwork report preparation and submit to the HOD and Management.
13. Overall responsibility for the planning, performing, reporting and archiving of the study.
14. Ensure equipment qualification of instruments used in Genotoxicology and prepare user specification for Genotoxicology instruments and equipment to be procured for the department.
15. Ensure all equipment and instruments are maintained in calibrated status. Monitor and maintain the equipment’s and instruments used in laboratory to avoid misuse and ensure minimum downtime for instruments by preventive maintenance Programme.
16. Check the studies for the Compliance to the regulatory requirements.
17. Coordinating with QA during the facility audits and study based inspections.
Location : Hyedrabad
Designation :
Research Associate/Sr. Research Associate
Desired Qualification & Experience
MVSc (Veterinary Pathology) & 1-5 Years’ Experience in Pharmaceutical Industry CRO/Discovery Research
Job Description :
1. Performing Gross pathology, organ weighing and histopathology evaluation and report preparation for rodents and non-rodents
2. Histopathology evaluation, interpretation and report writing
3. Monitoring equipment’s used in clinical pathology and histopathology for calibration and validation status
4. Quality control of slides in histopathology section
5. Detailed clinical examination and ophthalmic observation of study animals
6. Preparation and review of Standard Operating Procedures
7. Function as study veterinarian/study personnel
8. Veterinary care services as and when required.
Location : Hyedrabad
For further queries log in to careers @vimta.com
Interested Candidates can drop your CV at
hr@vimta.com or pvrao@vimta.com
Designation :
Scientist
Desired Qualification & Experience
2 - 5 years
Job Description :
Experience in characterization of proteins using cell based assays and analytical methodologyMust have experience in assay development and validationExperience in handling instruments such as HPLC, ELISA Reader, qPCR, MALDI-TOF, etc is desirable
Location : Hyedrabad
Department : Biopharma
Designation :
Group Leader
Desired Qualification & Experience
M.Pharm/M.Tech/M.Sc in Biotechnology & 8-9 years
Job Description :
Experience in instruments like HPLC/ELISAReader/QPCR/CE/MALDI-TOF/ESI-MSExperience in core projects / assignments like Immunogenicity/PKMethod Development & Validation of Preclinical & ClinicalSamples for Proteins & mAbsExperience in Physiochemical & Cell Based Bioassays for mAbs & Proteins
Department : Biopharma
Division : Pre - Clinical
Designation :
Research Associate/Sr. Research Associate/Scientist/Sr. Scientist - Animal House
Desired Qualification & Experience :
M. V. Sc / B. V. Sc (Veterinary & AH) & 0-12 years of experience in toxicology.
Job Description :
Primary Responsibilities:
Animal House VeterinarianResponsible for day to day functioning of Animal Facility and Breeding of laboratory animalsFollow proper quarantine procedure to ensure release of good quality animals into the experiment areaEnsure proper veterinary care for research animals including rodents, rabbits, Guinea pigs and dogs consistent with guidelines established by the CPCSEA, AAALAC requirementsProvide and maintain high quality clinical health care and record keeping for all laboratory activities and support team investigators conduct and surgical proceduresEnsure proper waste management and disposal system as per the requirements of the local pollution boardInteraction with the Purchase, Analytical, Facility in-charge and QA to ensure proper upkeep of the Animal HousePlan and supply appropriate animals for testing by putting in place a proper animal procurement, breeding and holding programs so as to facilitate uninterrupted supply of animals to various groups in pre-clinical divisionIdentity and create effective networking for procurement of animals and other resources needed for day -to-day management of the Animal HouseUp -to-date maintenance of all documents pertaining to CPCSEA forms, quarantine, health checkups, maintenance, procurement of animals, feed, water and bedding material analysis data and inventory, accessories, breeding, supply, euthanasia, disposal of animals and animal house materialsProactive preparation and planning of audits from internal or external QA, sponsors, regulatory authorities, certification authorities and TFF. Provide effective mechanisms for effective furnishing of related data to facilitate proper scrutinyAs a study veterinarian will be responsible for the welfare of the animals during conduct of the study and ensure that undue pain is not inflicted to the animals by the experimenterTo review or prepare all Animal House related SOPsResponsible for maintenance of training records of all animal housePlanning of activities during weekly offs and holidays in advancePreparation of healthy status report on animal inventoryPreparation of animal report for AAALAC submission
Secondary Responsibilities:
Monitor compliance of quality procedures and appropriate corrective actions to be taken on issuesTo train technical staff in animal handling and other animal husbandry activitiesUndertake internal quality audits and take corrective action to rectify deficienciesCoordinating with Purchase department for timely deliveries
Designation :
Research Associate/Sr. Research Associate/Scientist/Sr. Scientist/Group Leader - Genotoxicology
Desired Qualification & Experience :
M. Pharmacy Pharmacology / M. Sc Microbiology / M. Sc Toxicology & 1 – 13 Years
Job Description :
1. Study Director / Study Coordinator for In Vitro and In Vivo Genotoxicology studies
2. Validation of Core battery studies in Genetic Toxicology in accordance with OECD GLP norms
3. To monitor all aspects of studies and be an effective link between the testing facility and sponsor and coordinate from initiation of client discussion till termination of the project as a project manager
4. Experimental trial designing, conducting, coordinating and supervising the In Vitro and In Vivo Genotoxicology studies for various test substances using different test system/cell lines
5. Preparation, review and approval of protocols, progress reports, summary, interim reports, and detailed schedules for the In Vitro and In Vivo Genotoxicology studies. Maintenance and propagation of various established cell lines as per GLP compliance for Genetic toxicology studies
6. Maintenance and sub culturing of various bacterial tester strains for Bacterial Reverse Mutation Assay
7. Train Study Personnel in Proof of Concept (POC) animal models and GLP related documentation and report preparation
8. Plan, perform, conduct and monitor the core batteries of Genotoxicology studies
9. Coordinating with the in-vitro Toxicology team in standardization and new method validation of cytotoxicity assays
10. Communication with Management and sponsors related to the study issues.
11. Preparation of Study proposal (quotation), Study plan, Standard operating procedures and Study status to sponsor’s
12. To lead a team of people, weekly and monthly teamwork report preparation and submit to the HOD and Management
13. Overall responsibility for the planning, performing, reporting and archiving of the study
14. Ensure equipment qualification of instruments used in Genotoxicology and prepare user specification for Genotoxicology instruments and equipment to be procured for the department
15. Ensure all equipment and instruments are maintained in calibrated status. Monitor and maintain the equipment’s and instruments used in laboratory to avoid misuse and ensure minimum downtime for instruments by preventive maintenance Programme.
16. Check the studies for the Compliance to the regulatory requirements
17. Coordinating with QA during the facility audits and study based inspections
Location : Hyedrabad
Designation :
Sr. Research Associate/Scientist/Sr. Scientist/Group Leader/Deputy Manager – Genetic Toxicology In Vitro Lab
Desired Qualification & Experience :
M. Pharmacy Pharmacology / M. Sc Microbiology / M. Sc Toxicology & 3 – 12 Years
Job Description :
1. Study Director / Study Coordinator for In Vitro and In Vivo Genotoxicology studies.
2. Validation of Core battery studies in Genetic Toxicology in accordance with OECD GLP norms.
3. To monitor all aspects of studies and be an effective link between the testing facility and sponsor and coordinate from initiation of client discussion till termination of the project as a project manager.
4.Experimental trial designing, conducting, coordinating and supervising the In Vitro and In Vivo Genotoxicology studies for various test substances using different test system/cell lines.
5. Preparation, review and approval of protocols, progress reports, summary, interim reports, and detailed schedules for the In Vitroand In Vivo Genotoxicologystudies. Maintenance and propagation of various established cell lines as per GLP compliance for Genetic toxicology studies.
6. Maintenance and sub culturing of various bacterial tester strains for Bacterial Reverse Mutation Assay.
7. Train Study Personnel in Proof of Concept (POC) animal models and GLP related documentation and report preparation.
8. Plan, perform, conduct and monitor the core batteries of Genotoxicology studies.
9. Coordinating with the in-vitro Toxicology team in standardization and new method validation of cytotoxicity assays.
10. Communication with Management and sponsors related to the study issues.
11. Preparation of Study proposal (quotation), Study plan, Standard operating procedures and Study status to sponsor’s.
12. To lead a team of people, weekly and monthly teamwork report preparation and submit to the HOD and Management.
13. Overall responsibility for the planning, performing, reporting and archiving of the study.
14. Ensure equipment qualification of instruments used in Genotoxicology and prepare user specification for Genotoxicology instruments and equipment to be procured for the department.
15. Ensure all equipment and instruments are maintained in calibrated status. Monitor and maintain the equipment’s and instruments used in laboratory to avoid misuse and ensure minimum downtime for instruments by preventive maintenance Programme.
16. Check the studies for the Compliance to the regulatory requirements.
17. Coordinating with QA during the facility audits and study based inspections.
Location : Hyedrabad
Designation :
Research Associate/Sr. Research Associate
Desired Qualification & Experience
MVSc (Veterinary Pathology) & 1-5 Years’ Experience in Pharmaceutical Industry CRO/Discovery Research
Job Description :
1. Performing Gross pathology, organ weighing and histopathology evaluation and report preparation for rodents and non-rodents
2. Histopathology evaluation, interpretation and report writing
3. Monitoring equipment’s used in clinical pathology and histopathology for calibration and validation status
4. Quality control of slides in histopathology section
5. Detailed clinical examination and ophthalmic observation of study animals
6. Preparation and review of Standard Operating Procedures
7. Function as study veterinarian/study personnel
8. Veterinary care services as and when required.
Location : Hyedrabad
For further queries log in to careers @vimta.com
Interested Candidates can drop your CV at
hr@vimta.com or pvrao@vimta.com
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Extension of Last Date for submission of Online Application of CSIR - UGC Test.
The test that changed the career and life of 100s of 1000s of people is back. Don't forget to apply whether you are doing MSc,M Tech or B Tech . Working as project assistant ? Don't be lazy , prepare and write CSIR , it is never too late. Even if you don't get the fellowship a pass can make you a reacher or register and get fellowships from grants. Apply online on
http://WWW.Csirhrdg.res.in
COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH
HUMAN RESOURCE DEVELOPMENT GROUP
EXAMINATION UNIT
C.S.I.R. Complex, H.R.D. Group, library Avenue, Pusa, New Delhi-110012
NOTIFICATION
EXTENSION OF LAST DATE FOR SUBMISSION OF ONLINE APPLICATION FORM
FOR JOINT CSIR-UGC TEST FOR JUNIOR RESEARCH FELLOWSHIP & ELIGIBILITY
FOR LECTURESHIP (NET) SCHEDULED ON 17TH DECEMBER, 2017
It is notified that the last date for submission of Online Application form for Joint CSIR-UGC Test for
Junior Research Fellowship and Eligibility for Lectureship (NET) December, 2017 has been extended up
to 23.09.2017
Pls. Refer the following advertisement :
http://WWW.Csirhrdg.res.in
COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH
HUMAN RESOURCE DEVELOPMENT GROUP
EXAMINATION UNIT
C.S.I.R. Complex, H.R.D. Group, library Avenue, Pusa, New Delhi-110012
NOTIFICATION
EXTENSION OF LAST DATE FOR SUBMISSION OF ONLINE APPLICATION FORM
FOR JOINT CSIR-UGC TEST FOR JUNIOR RESEARCH FELLOWSHIP & ELIGIBILITY
FOR LECTURESHIP (NET) SCHEDULED ON 17TH DECEMBER, 2017
It is notified that the last date for submission of Online Application form for Joint CSIR-UGC Test for
Junior Research Fellowship and Eligibility for Lectureship (NET) December, 2017 has been extended up
to 23.09.2017
Pls. Refer the following advertisement :
↧
8th International Conference of LASA , New Delhi India
Laboratory Animal Scientist's Association ( LASA ) inviting you on its 8th International Conference in New Delhi , India on Recent Advances in 3 R's and Laboratory Animal Science which is being jointly organized by Jawaharlal Nehru University ( JNU ) , CSIR - Institute of Genomics & Integrative Biology (CSIR - IGIB ) and National Institute of Biologicals (NIB) in Delhi on 25th to 26th November , 2017.
This event will comprise of lectures from renowned keynote speakers , oral presentations and poster sessios related to the theme of the conference i.e. 3 R's and Laboratory Animal Science.
Representation from various CRO's , Pharmaceutical and Biotechnology industries along with eminent International speakers are also expected to participate in the conference.
For further information , you may visit official website of LASA :
http://lasacon2017.com/
This event will comprise of lectures from renowned keynote speakers , oral presentations and poster sessios related to the theme of the conference i.e. 3 R's and Laboratory Animal Science.
Representation from various CRO's , Pharmaceutical and Biotechnology industries along with eminent International speakers are also expected to participate in the conference.
For further information , you may visit official website of LASA :
http://lasacon2017.com/
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Job opportunities at Stelis Biopharma , Bangalore , India
Walkin drive for Sterile Biotech Manufacturing
Date: 24th Sept 2017
Venue : St.Francis College for Women, Street No. 6, Uma Nagar, Begaumpet, Hyderagad, Telangana - 500016
Candidate in time : 8 am to 12.30 pm
Job Location : Yelahanka ,Bangalore India
Requirments:
Designation : Associate / Senior - Associate
Qualification :
B. Pharma / M. Pharma / M. Sc / B.Tech / M.Tech - Biotechnology , Biochemical / B.E - Chemical Engineering
- 3 to 7 years of experience in DP product- Fill Finish (Maufacturing)
Designation : Associate / Senior Associate
Qualification :
B. Pharma / M. Pharma / M. Sc / B.Tech / M.Tech - Biotechnology , Biochemical / B.E - Chemical Engineering
- 3 to 7 years of experience as Formulation incharge
Designation : Associate / Senior Associate / Team Lead
Qualification :
B. Pharma / M. Pharma / M. Sc / B.Tech / M.Tech - Biotechnology , Biochemical / B.E - Chemical Engineering
- 3 to 10 years experience as Component preparation and disinfectant prep & inchanrge
Designation : Associate / Senior Associate
Qualification :
B. Pharma / M. Pharma / M. Sc / B.Tech / M.Tech - Biotechnology , Biochemistry , Microbiology
-3 to 7 years of experience as Visual inspection and packing team member
Designation : Associate / Senior Associate
Qualification :
B. Pharma / M. Pharma / M. Sc / B.Tech / M.Tech - Biotechnology , Biochemical / B.E - Chemical Engineering
- 3 to 10 years experience as Manufacturing QMS and compliance in charge
Designation : Associate / Senior Associate / Team Lead
Qualification :
B. Pharma / M. Pharma / M. Sc / B.Tech / M.Tech - Biotechnology , Biochemical / B.E - Chemical Engineering / Process Engineering / Production Engineering
-3 to 10 years experience as DP process engineering in charge
Designation : Associate / Senior Associate
Qualification :
B. Pharma / M. Pharma / M. Sc or Post Graduate in Material Management / MBA in Supply Chain Management
- 3 to 7 years of experience as DP warehouse team member and in charge.
Documents to be carried: Resume, Latest Salary break-up letter & 3 Pay Slips; 1 Passport Size Photo, ID Proof, Highest Educational Certificates and Mark sheets.
Date: 24th Sept 2017
Venue : St.Francis College for Women, Street No. 6, Uma Nagar, Begaumpet, Hyderagad, Telangana - 500016
Candidate in time : 8 am to 12.30 pm
Job Location : Yelahanka ,Bangalore India
Requirments:
Designation : Associate / Senior - Associate
Qualification :
B. Pharma / M. Pharma / M. Sc / B.Tech / M.Tech - Biotechnology , Biochemical / B.E - Chemical Engineering
- 3 to 7 years of experience in DP product- Fill Finish (Maufacturing)
Designation : Associate / Senior Associate
Qualification :
B. Pharma / M. Pharma / M. Sc / B.Tech / M.Tech - Biotechnology , Biochemical / B.E - Chemical Engineering
- 3 to 7 years of experience as Formulation incharge
Designation : Associate / Senior Associate / Team Lead
Qualification :
B. Pharma / M. Pharma / M. Sc / B.Tech / M.Tech - Biotechnology , Biochemical / B.E - Chemical Engineering
- 3 to 10 years experience as Component preparation and disinfectant prep & inchanrge
Designation : Associate / Senior Associate
Qualification :
B. Pharma / M. Pharma / M. Sc / B.Tech / M.Tech - Biotechnology , Biochemistry , Microbiology
-3 to 7 years of experience as Visual inspection and packing team member
Designation : Associate / Senior Associate
Qualification :
B. Pharma / M. Pharma / M. Sc / B.Tech / M.Tech - Biotechnology , Biochemical / B.E - Chemical Engineering
- 3 to 10 years experience as Manufacturing QMS and compliance in charge
Designation : Associate / Senior Associate / Team Lead
Qualification :
B. Pharma / M. Pharma / M. Sc / B.Tech / M.Tech - Biotechnology , Biochemical / B.E - Chemical Engineering / Process Engineering / Production Engineering
-3 to 10 years experience as DP process engineering in charge
Designation : Associate / Senior Associate
Qualification :
B. Pharma / M. Pharma / M. Sc or Post Graduate in Material Management / MBA in Supply Chain Management
- 3 to 7 years of experience as DP warehouse team member and in charge.
Documents to be carried: Resume, Latest Salary break-up letter & 3 Pay Slips; 1 Passport Size Photo, ID Proof, Highest Educational Certificates and Mark sheets.
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Job Opportunities at Syngene International Limited , Bangalore , India
Recruitment drive by Syngene For ( Biopharmaceutical R&D ) Upstream R&D , MSAT , Drug Product Development , Analytical R&D and Downstream R&D on 23rd (Mumbai ) and 24th ( Pune ) September 2017.
Upstream R&D
Qualification :
PhD with 1-3 yrs. Of industrial experience
MSAT
Qualification :
M.Tech / MSc with 2 - 5 yrs. Of experience in Upstream or downstream from PD or manufacturing.
Drug Product Development
Qualification :
M.Tech / MSc. / M.Pharma With 5 - 7 yrs. Of industrial experience in the protein formulation area.
Analytical R&D
Qualification :
M.Tech / M.Sc ( Biotechnology / Microbiology / Life Sciences ) with 3 - 10 yrs. of experience (OR) PhD ( Life Sciences / Biotechnology ) with 0 - 3 yrs. of experience.
Downstream R&D
Qualification :
Master's in Life Sciences / Engineering or relevant field with 5 - 9 yrs. of industrial experience in the protein purification area.
Date : 23rd September 2017
Time : 8.30 AM
Venue : Mirage Hotel , Andheri - Kurla road , Navpada , Marol , Andheri East ,
Mumbai , Maharashtra - 400047
Date : 24th September 2017
Time : 8.30 AM
Venue : Hotel Radisson Blu, Plot no. 136 /1, Behind Mercedes Benz International School , Phase - 1 , Hinjewadi,
Pune - Maharashtra - 411057
Required Documents :. Copy of resume , 3 months salary slips , Annual CTC Breakup Sheet and 1 Passport size Photograph.
For further queries log in to careers @syngeneintl.com
Upstream R&D
Qualification :
PhD with 1-3 yrs. Of industrial experience
MSAT
Qualification :
M.Tech / MSc with 2 - 5 yrs. Of experience in Upstream or downstream from PD or manufacturing.
Drug Product Development
Qualification :
M.Tech / MSc. / M.Pharma With 5 - 7 yrs. Of industrial experience in the protein formulation area.
Analytical R&D
Qualification :
M.Tech / M.Sc ( Biotechnology / Microbiology / Life Sciences ) with 3 - 10 yrs. of experience (OR) PhD ( Life Sciences / Biotechnology ) with 0 - 3 yrs. of experience.
Downstream R&D
Qualification :
Master's in Life Sciences / Engineering or relevant field with 5 - 9 yrs. of industrial experience in the protein purification area.
Date : 23rd September 2017
Time : 8.30 AM
Venue : Mirage Hotel , Andheri - Kurla road , Navpada , Marol , Andheri East ,
Mumbai , Maharashtra - 400047
Date : 24th September 2017
Time : 8.30 AM
Venue : Hotel Radisson Blu, Plot no. 136 /1, Behind Mercedes Benz International School , Phase - 1 , Hinjewadi,
Pune - Maharashtra - 411057
Required Documents :. Copy of resume , 3 months salary slips , Annual CTC Breakup Sheet and 1 Passport size Photograph.
For further queries log in to careers @syngeneintl.com
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Career in biotechnology after 12 without maths
Hi everyone
This is my first post in group
I am student of class 12 BPC
Want to move ahead with biotechnology, microbiology, genetics
Pl suggest me some
List of course after 12 like BSc,btech
Name of good colleges
Thanks
Sanjana
9619590588
This is my first post in group
I am student of class 12 BPC
Want to move ahead with biotechnology, microbiology, genetics
Pl suggest me some
List of course after 12 like BSc,btech
Name of good colleges
Thanks
Sanjana
9619590588
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TIFR
Anybody applied fr tifr -gs exam?????
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Previous year Question Papers for IIT JAM
Links for :
IIT JAM Biotechnology Papers
2014 :
http://jam.iitd.ac.in/PDFs/BT_QP_2014.pdf
2015 :
http://jam.iitd.ac.in/PDFs/BT_QP_2015.pdf
2016 :
http://jam.iitd.ac.in/PDFs/BT_QP_2016.pdf
Biological Sciences Papers
2014 :
http://jam.iitd.ac.in/PDFs/BL_QP_2014.pdf
2015 :
http://jam.iitd.ac.in/PDFs/BL_QP_2015.pdf
2016 :
http://jam.iitd.ac.in/PDFs/BL_QP_2016.pdf
IIT JAM Biotechnology Papers
2014 :
http://jam.iitd.ac.in/PDFs/BT_QP_2014.pdf
2015 :
http://jam.iitd.ac.in/PDFs/BT_QP_2015.pdf
2016 :
http://jam.iitd.ac.in/PDFs/BT_QP_2016.pdf
Biological Sciences Papers
2014 :
http://jam.iitd.ac.in/PDFs/BL_QP_2014.pdf
2015 :
http://jam.iitd.ac.in/PDFs/BL_QP_2015.pdf
2016 :
http://jam.iitd.ac.in/PDFs/BL_QP_2016.pdf
↧
What is GATE XL?
Hello sir,
I am A.Roopakala.What is gate xl? I am pursuing fourth year from the department of biotechnology.I have started preparation but only 4 mnths are left.So can u Suggest me some tips where I can cover the max of the syllabus so that I would score well.U gave a link regarding important topics for gate 2017.In d same way can u share the important topics for gate bt 2018.
I am A.Roopakala.What is gate xl? I am pursuing fourth year from the department of biotechnology.I have started preparation but only 4 mnths are left.So can u Suggest me some tips where I can cover the max of the syllabus so that I would score well.U gave a link regarding important topics for gate 2017.In d same way can u share the important topics for gate bt 2018.
↧
Dengue Antibodies Act as Vaccine Against Zika
Researchers from Imperial College London and Washington University in St Louis conducted an important experiment to test the impact of Antibodies taken from the patients infected with Dengue virus, on early stage Zika patients (in this case, a mouse model).
And, interestingly those antibodies not only prevented infection in Zika-infected mice, but also protected the fetus of female mice from the infection. This discovery can be path-breaking if replicated in humans as well; as it can lead to emergence of a single vaccine for both the viral diseases.
The research and the findings make sense as both Zika and Dengue are caused by the viruses belonging to Flaviviridae family (and in fact are transmitted by the same species of mosquito as well!). The entire study has been published in Nature Immunology in Aug 2017 under the title:
Human antibodies to the dengue virus E-dimer epitope have therapeutic activity against Zika virus infection
Following is the abstract taken from the publication (Nature Immunology):
Refer the journal for full details:
http://www.nature.com/ni/journal/vaop/nc....3849.html
And, interestingly those antibodies not only prevented infection in Zika-infected mice, but also protected the fetus of female mice from the infection. This discovery can be path-breaking if replicated in humans as well; as it can lead to emergence of a single vaccine for both the viral diseases.
The research and the findings make sense as both Zika and Dengue are caused by the viruses belonging to Flaviviridae family (and in fact are transmitted by the same species of mosquito as well!). The entire study has been published in Nature Immunology in Aug 2017 under the title:
Human antibodies to the dengue virus E-dimer epitope have therapeutic activity against Zika virus infection
Following is the abstract taken from the publication (Nature Immunology):
Quote:The Zika virus (ZIKV) epidemic has resulted in congenital abnormalities in fetuses and neonates. Although some cross-reactive dengue virus (DENV)-specific antibodies can enhance ZIKV infection in mice, those recognizing the DENV E-dimer epitope (EDE) can neutralize ZIKV infection in cell culture. We evaluated the therapeutic activity of human monoclonal antibodies to DENV EDE for their ability to control ZIKV infection in the brains, testes, placentas, and fetuses of mice. A single dose of the EDE1-B10 antibody given 3 d after ZIKV infection protected against lethality, reduced ZIKV levels in brains and testes, and preserved sperm counts. In pregnant mice, wild-type or engineered LALA variants of EDE1-B10, which cannot engage Fcg receptors, diminished ZIKV burden in maternal and fetal tissues, and protected against fetal demise. Because neutralizing antibodies to EDE have therapeutic potential against ZIKV, in addition to their established inhibitory effects against DENV, it may be possible to develop therapies that control disease caused by both viruses.
Refer the journal for full details:
http://www.nature.com/ni/journal/vaop/nc....3849.html
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More Pages to Explore .....
