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Careers

Would you like to be a part of an organization that is devoted to excellence in quality and uncompromising integrity in its service? If yes, read on. In our fervor to realize our vision, we are looking for talented, experienced professionals who have a taste for excellence and who never want to stop learning. As a multi disciplinary scientific organization, VIMTA gives its people an experience in a variety of scientific fields. We encourage our people to constantly improve their knowledge and skills and to this end we conduct ongoing training programs in various ways

VIMTA is an equal opportunity employer and provides excellent working environment with competitive salaries commensurate with experience and education

Our current career opportunities:

Preclinical:

Job Title

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 Profile

Primary Responsibilities:

    • Animal House Veterinarian
    • Responsible for day to day functioning of Animal Facility and Breeding of laboratory animals
    • Follow proper quarantine procedure to ensure release of good quality animals into the experiment area
    • Ensure proper veterinary care for research animals including rodents, rabbits, Guinea pigs and dogs consistent with guidelines established by the CPCSEA, AAALAC requirements
    • Provide and maintain high quality clinical health care and record keeping for all laboratory activities and support team investigators conduct and surgical procedures
    • Ensure proper waste management and disposal system as per the requirements of the local pollution board
    • Interaction with the Purchase, Analytical, Facility in-charge and QA to ensure proper upkeep of the Animal House
    • Plan 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 division
    • Identity and create effective networking for procurement of animals and other resources needed for day -to-day management of the Animal House
    • Up -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 materials
    • Proactive 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 scrutiny
    • As 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 experimenter
    • To review or prepare all Animal House related SOPs
    • Responsible for maintenance of training records of all animal house
    • Planning of activities during weekly offs and holidays in advance
    • Preparation of healthy status report on animal inventory
    • Preparation of animal report for AAALAC submission

Secondary Responsibilities:

  • Monitor compliance of quality procedures and appropriate corrective actions to be taken on issues
  • To train technical staff in animal handling and other animal husbandry activities
  • Undertake internal quality audits and take corrective action to rectify deficiencies
  • Coordinating with Purchase department for timely deliveries
Location Hyderabad
Division Preclinical Division
Department Preclinical
 
Job Title

Research Associate/Sr. Research Associate/Scientist/Sr. Scientist - DMPK

Desired Qualification & Experience M. Pharmacy in Pharmacology & 1-12 years of experience in toxicology
Job Profile
  • In vivo and in vitro DMPK phase of preclinical studies, which includes the following activities
  • Conducting In vivo PK studies in various species such as Mice, Rat and Dog
  • Hands on experience in conducting In vitro metabolism and absorption studies using sub-cellular fractions and cell lines, respectively
  • Planning and reviewing the study plans/protocols
  • Reviewing raw data and study reports
  • Archiving the DMPK studies
  • Maintenance of time lines of the projects
  • Preparation of costing of studies
  • Writing, reviewing and revision of standard operating procedures (SOP’s)
  • Qualification/costing assessment for the purchase of new equipment
  • Coordinate scientific discussions with sponsor/client from starting a project till the termination of the project as a project manager
  • Communication with QA during the facility audit and study based inspections
  • Coordinate/stand audit trials with sponsors and regulatory bodies
  • Communication with management and sponsor regarding study related issues
Location Hyderabad
Division Preclinical Division
Department Preclinical
 
Job Title

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 Profile
  • 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 Hyderabad
Division Preclinical Division
Department Preclinical
 
Job Title

Research Associate/Sr. Research Associate/Scientist/Sr. Scientist/Group Leader - Toxicology

Desired Qualification & Experience M. Pharmacy in Pharmacology (Toxicology) & 1-12 years of experience in toxicology
Job Profile
  • Experience of conducting different types of toxicity study (acute, 14-day or 28-day toxicity study, reproductive toxicity studies) Handling of laboratory animals (rat, mice, dogs, rabbits, guinea pigs)
  • Dosing of laboratory animals by different routes
  • General/clinical observation of animals
  • Collection of organs
  • Interpretation of toxicity study data and report preparation Understanding of GLP
Location Hyderabad
Division Preclinical Division
Department Preclinical
 
Job Title

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 Profile
  • 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 Hyderabad
Division Preclinical Division
Department Preclinical
 
Job Title

Research Associate/Sr. Research Associate/ Scientist/Sr. Scientist/Group Leader

Desired Qualification & Experience M. Pharmacy in Pharmacology (Toxicology) & 2-12 years of experience in toxicology ( General and Genetic tox )
Job Profile
  • 1. Experience of conducting different types of toxicity study (acute, 14-day or 28-day toxicity study, reproductive toxicity studies) Handling of laboratory animals (rat, mice, dogs, rabbits, guinea pigs)
  • 2. Dosing of laboratory animals by different routes
  • 3. General/clinical observation of animals
  • 4. Collection of organs
  • 5. Interpretation of toxicity study data and report preparation Understanding of GLP.
Location Hyderabad
Division Preclinical Division
Department Preclinical - Toxicology
 
Job Title

Research Associate/Sr. Research Associate

Desired Qualification & Experience MVSc (Veterinary Pathology) & 1-5 Years’ Experience in Pharmaceutical Industry CRO/Discovery Research.
Job Profile
  • 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 Hyderabad
Division Preclinical Division
Department Preclinical - Pathology
 

" Interested Candidates can drop your CV at mahesh.namala@vimta.in and pvrao@vimta.com "


Clinical Reference Lab (CRL):

Job Title

Office Assistant

Desired Qualification & Experience Any Graduation - Fresher
Job Profile
  • 1. To monitor the Local sample collection boys.
  • 2. Update the day to day to material issues to PSC/DCs, Branch labs and mail the dispatch details to PSC/DCs & all concerned sales team.
  • 3. Prepare the list of sample collection boys for exp & salaries
  • 4. Preparation of indent for monthly materials requirement.
  • 5. Arrange the visiting cards to sales team as per their requirement.
  • 6. Other assigned works by HOD.
Location VLL- Cherlapally
Division CRL
Department Support Services
 

" Interested Candidates can drop your CV at jagadeesh.komiri@vimta.in and pvrao@vimta.com "


Business Development:

Job Title

AVP / Senior Manager / Manager – BD (Pharma)

Desired Qualification & Experience Qualification: Any specialization MBA/PGDM with Graduation in Chemistry / Life Sciences / Biotech / Biology / Food.
Experience: 13 to 20 years
Job Profile
  • a. Responsible for marketing of Vimta’s Pharma testing services to clients
  • b. Responsible for sales targets vis-à-vis achievements
  • c. Answering queries on phone / in person about Vimta services
  • d. Organizing / attending sales visits
  • e. Demonstrating / presenting Vimta services
  • f. Establishing new business
  • g. Maintaining accurate sales records through proper reporting
  • h. Attending trade exhibitions, conferences and meetings
  • i. Reviewing sales performance
  • j. Negotiating contacts.
  • k. Must be able to handle a team
Location Hyderabad
Division Support Services
Department Business Development
 
Job Title

Executive / Senior Executive – BD (Pharma)

Desired Qualification & Experience Qualification: Any specialization MBA/PGDM with Graduation in Chemistry / Life Sciences / Biotech / Biology / Food.
Experience: 7 to 12 years
Job Profile
  • a. Responsible for marketing of Vimta’s Pharma testing services to clients
  • b. Responsible for sales targets vis-à-vis achievements
  • c. Answering queries on phone / in person about Vimta services
  • d. Organizing / attending sales visits
  • e. Demonstrating / presenting Vimta services
  • f. Establishing new business
  • g. Maintaining accurate sales records through proper reporting
  • h. Attending trade exhibitions, conferences and meetings
  • i. Reviewing sales performance
  • j. Negotiating contacts.
Location Hyderabad, Bangalore
Division Support Services
Department Business Development
 
Job Title

Assistant Manager / Senior Executive – BD (Food)

Desired Qualification & Experience Qualification: Any specialization MBA/PGDM with Graduation in Chemistry / Life Sciences / Biotech / Biology / Food.
Experience: 6 to 11 years
Job Profile
  • a. Responsible for marketing of Vimta’s Pharma testing services to clients
  • b. Responsible for sales targets vis-à-vis achievements
  • c. Answering queries on phone / in person about Vimta services
  • d. Organizing / attending sales visits
  • e. Demonstrating / presenting Vimta services
  • f. Establishing new business
  • g. Maintaining accurate sales records through proper reporting
  • h. Attending trade exhibitions, conferences and meetings
  • i. Reviewing sales performance
  • j. Negotiating contacts.
Location Chennai, Ahmedabad, Hyderabad, Chandigarh, Guwahati, Kolkata
Division Support Services
Department Business Development
 
Job Title

Manager / Deputy Manager – BD (Food)

Desired Qualification & Experience Qualification: Any specialization MBA/PGDM with Graduation in Chemistry / Life Sciences / Biotech / Biology / Food.
Experience: 11 to 16 years
Job Profile
  • a. Responsible for marketing of Vimta’s Pharma testing services to clients
  • b. Responsible for sales targets vis-à-vis achievements
  • c. Answering queries on phone / in person about Vimta services
  • d. Organizing / attending sales visits
  • e. Demonstrating / presenting Vimta services
  • f. Establishing new business
  • g. Maintaining accurate sales records through proper reporting
  • h. Attending trade exhibitions, conferences and meetings
  • i. Reviewing sales performance
  • j. Negotiating contacts.
  • k. Must be able to handle a team
Location Hyderabad, Delhi, Goa
Division Support Services
Department Business Development
 
Job Title

Trainee Executive / Executive / Junior Executive – BD (Food)

Desired Qualification & Experience Qualification: Any specialization MBA/PGDM with Graduation in Chemistry / Life Sciences / Biotech / Biology / Food.
Experience: 0 to 5 years
Job Profile
  • a. Responsible for marketing of Vimta’s Food testing services to clients in Food industry
  • b. Responsible for sales targets vis-à-vis achievements
  • c. Answering queries on phone / in person about Vimta services
  • d. Organizing / attending sales visits
  • e. Demonstrating / presenting Vimta services
  • f. Establishing new business
  • g. Maintaining accurate sales records through proper reporting
  • h. Attending trade exhibitions, conferences and meetings
  • i Reviewing sales performance
  • j. Negotiating contacts
Location Jaipur, Coimbatore, Delhi, Mumbai, Hyderabad
Division Support Services
Department Business Development
 

" Interested Candidates can drop your CV at rajanikanth.medichalam@vimta.in and pvrao@vimta.com "


Quality Assurance:

Job Title

Quality Auditor (GLP)

Desired Qualification & Experience A minimum of postgraduate in Science/ Pharmacy with at least two years experience
Job Profile
  • Should be working as GLP auditor in a preclinical CRO/ in-house facility of a pharmaceutical/Chemical/Agrochemical. Should have a though understanding of principles of OECD/USFDA/EPA GLP and requirements of NGCMA. The candidate should have thorough understanding of OECD testing guidelines followed in testing of chemicals. Proficiency in spoken and writing English with good communication skills would be desirable
Location VLS
Division Support Services
Department Quality Assurance
 
Job Title

Quality Auditor (Microbiology - Food)

Desired Qualification & Experience A candidate with minimum of Post graduate in Microbiology with at least two years
Job Profile
  • Should have work experience in a testing lab or QC lab of a food lab. The candidate should have thorough understanding of requirements of good practices followed in food industry like HACCP; understanding of requirements of ISO/IEC 17025:2005 would desirable. The candidate should have thorough understanding of environmental requirements, various tests as per requirements of various guidelines like APHA, IS etc. Proficiency spoken and writing English with good communication skills would be desirable
Location VLS
Division Support Services
Department Quality Assurance
 
Job Title

Dy.Manager/Manager – QA (Pharma)

Desired Qualification & Experience M.Sc./M.Pharm & 10-12 Years
Job Profile
  • In depth knowledge of cGMP (21 CFR Part 210 & 211)
  • Provide direction and leadership for QA Dept. to improve their performance and meet divisional and overall Company goals.
  • A very good understanding of validation/qualification requirements; change management; deviation control and management; investigations & CAPAs, documentation requirements etc.
  • Design and implement strategies for capability building and innovation of new services.
  • Provide management with reports on QA activities and findings
  • Plan and conduct internal audits, study audits and routine process audits for pre-clinical studies as per cGMP requirements
  • Host external audits
  • Ensure timely and effective CAPAs
  • Write and review SOPs. Proactively focus on quality system improvements
  • Review study reports
  • Ensure compliance to GMPs and Company’s quality system requirements in the Laboratory
  • Assist VP / AVP-QA in technical and admin. assignments.
Location Hyderabad
Division Support Services
Department Quality Assurance
 
Job Title

Quality Auditor (Pharma)

Desired Qualification & Experience M.Pharm /B.Pharma & 1-4 Years
Job Profile
  • Conduct study and process audits to verify that the department’s systems, processes and outcomes comply to
  • Company Management System requirements (MSDs, Policies, MSPs, SOPs etc)
  • Applicable guidelines and GXPs
  • Regulatory requirements and customer requirements
  • Identify, document and report findings including any deviations and nonconforming work; communicate the findings to the auditee, Head Of the Division/Department and Quality Manager. Escalate to Management through Quality Manager, where resolutions of audit findings are adequate
  • Randomly review raw data and reports to verify their compliance to SOPs and customer contract requirements. Report any deviations to HOD and Quality Manager.
  • Participate in investigation of deviations &OOX results.
  • Review all QC raw data and results. Ensure corrective actions are taken for any poor unsatisfactory results.
  • Verify calibration data of equipments and ensure that all equipments are maintained in calibrated status.
  • Verify qualification data of equipments and ensure that all equipments are maintained in validated status.
  • Monitoring the GMP compliance in the laboratory.
  • Review of training recordsof department personnel’s.
Location Hyderabad
Division Support Services
Department Quality Assurance
 

" Interested Candidates can drop your CV at sanju.rathod@vimta.in and pvrao@vimta.com "


Analytical Division:

Job Title

Manager – Food and Water Lab

Desired Qualification & Experience Qualification:

1. Ph.D. in Chemistry with 7-10 years of experience in Food and Water lab

2. M.Sc., Chemistry with 8-12 years of experience in Food and Water lab

Experience: 7 to 12 years
Job Profile

The Dy. Manager / Manager – Food &Water Dept. (Analytical Division) maintains operational responsibilities for the activities that are related to Food, Water, Trace Analysis related to Foods, water and Agri. products

The competencies required are ………

  • ­ Design, implement and maintain quality practices and procedures for the management of the department services and integrity of operations. Ensure operations are performed according to contractual requirement and fully meet current GXPs, ISO 17025, as applicable and VIMTA’s policies and management system requirements
  • ­ Implement and proactively monitor for compliance to all applicable quality systems/regulations such as ISO 17025, GXPs,VIMTA’s policies and management system requirements in addition to meeting customer contractual requirements.
  • ­ Focus on continuous quality improvement and KPIs improvement
  • ­ Review Internal and External Audit Reports, PT/ILC Reports and advise effective CAPAs, for timely implementation, as required
  • ­ And many more……
Location Hyderabad, Ahmedabad, Indore, Bhimavaram, Vizag
Division Analytical Division
Department Food and Water Lab
 
Job Title

Scientist/ Sr. Scientist (Trace Analysis - Pharma)

Desired Qualification & Experience M.Sc./ M.Pharm./ B. Pharm. & 1 Years to 6 Years
Job Profile
  • 1. Method development and validation of elemental analysis in different Pharma samples by using Spectrometers.
  • 2. Perform analysis of trace metals in pharmaceuticals samples (any stage) of various matrix compositions in accordance with USP General Chapters and ICH guidelines.
  • 3. Method validations, Method optimizations and Method verifications done for finished products, Injectables and API’s by using ICP-MS & ICP OES
  • 4. Leachable and Extractable studies by using ICP-MS & ICP OES
  • 5. Involved in Delamination Studies.
  • 6. Analysis of different Pharma samples and food samples by using ICPOES as per customer supplied STP’s and in-house validated protocols.
  • 7. Analysing assay and relative substances by using ICPOES & ICPMS
  • 8. Analysis of heavy metal impurities of different Pharma samples and food samples by using ICP MS, ICP OES
  • 9. Protocols, Reports and STP’s preparations for elemental analysis by using ICP-MS.
  • 10. Investigation of Incidents, Occurrences and OOX results to find the root cause.
  • 11. Having experience on Blood sample, on ICP-MS.
  • 12. Calibration of analytical instruments (Analytical balance, ICPOES, ICP MS).
  • 13. Routine sample analysis
  • 14. In-process Sample Analysis
  • 15. Raw Material
Location Hyderabad
Division Analytical
Department Trace Analysis - Pharma
 

" Interested Candidates can drop your CV at suryavamsi.vasireddy@vimta.com and pvrao@vimta.com "