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Job Opportunities at Vimta labs Ltd. Hyedrabad
#1
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
Regards ,
Lavkesh Sharma

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