&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Medical Investigator - Vimta Labs Ltd, Cherlapally Qualification: MBBSCTC: As per market standardsLooking candidates from Clinical Research Organization only.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Primary Responsibilities:&nbsp;1.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Ensures that Good Clinical Practices (GCP) are followed.&nbsp;2.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Conduct planned studies as per protocol requirements, quality system procedures and SOPs.3.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Review of pre study health records.4.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Obtain written informed consent before each Volunteer participation in the trial.5.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Ascertaining that clinical data is complete, accurate and is recorded as per protocol and SOP requirements.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;6.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Assessment and documentation of UDS reports &amp; additional test reports.7.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Documentation of eligibility status.8.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Verification of daily Temperature log, Urotherm reading, Emergency medication kit documentation and expired medication discarding.9.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Briefing research staff on conducting the trail and Group briefing of ICF to volunteers10.&nbsp;AE, SAE management, reporting and documentation.11.&nbsp;Monitoring the trial throughout its duration.12.&nbsp;Verifying the data entered on to the CRFs is consistent with source data.13.&nbsp;ICU maintenance including management of emergency conditions.14.&nbsp;Monitoring of Vitals documentation, ECG, Phlebotomy and X-ray procedures.15.&nbsp;Verification of X ray films and X ray report destruction.16.&nbsp;Post study reports assessments and documentation.17.&nbsp;Completion status of CRFs and documentation.&nbsp;Secondary Responsibilities:1.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Review of ICFs, CRFs.2.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Screening and Evaluation of Volunteers for study participation.3.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Monitoring of drug administration to volunteers. Interested candidates can share their resumes to keerthana.rojanala@vimta.com.

Scientist (Bioanalytical) - Vimta Labs, Hyderabad Experience: 4-6 yearsCTC: 4-5 LPAWork Location: Cherlapally. Reports to: HODPrimary Responsibilities:1.&nbsp;&nbsp;Performance of Method Development, Validation and Study Sample Analysis using LC-MS/MS systems.2.&nbsp;&nbsp;Operation, Calibrations and Maintenance of Pipettes, pH meter, Balance, HPLC, Dispensers and Turbo-Evaporators, Centrifuge, Solid-Phase Extraction and other Bioanalytical equipment's.3.Preparation of Method Validation Protocols, Method Validation Reports, Standard Test Procedures, SOPs and Bioanalytical Reports.4.&nbsp;&nbsp;Responsible for documentation as per in house SOPs and practices in raw data forms and logbooks.5.&nbsp;&nbsp;Compilation of Calibration Data, Bio analytical raw data forms and logbooks.6.&nbsp;&nbsp;Maintenance of Workplace.7.&nbsp;&nbsp;Reporting to supervisor/HOD about progress of the jobs assigned.8.&nbsp;&nbsp;Follow in-house procedures for safe disposal of waste generated in the lab.9.&nbsp;&nbsp;Recording the temperature and humidity in the lab.	10.&nbsp;To ensure all applicable SOPs are being complied for the work being done.11.&nbsp;To ensure that raw data and other documents are recorded appropriately reflecting actual sequence of events.12.&nbsp;To ensure that all the results are being transcribed, reported and calculated appropriately matching with chromatographic data and raw data.13.&nbsp;Maintain cleanliness and safety aspects in the Lab.Secondary Responsibilities:1.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;To ensure proper labelling for all the reagents, solutions and chemicals in the laboratory.2.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Maintenance of Columns and Reference Standards in the lab.	3.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Ensure the archival of all completed study and validated documents.4.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Any other responsibility assigned by HOD. Interested candidates can share their profiles to keerthana.rojanala@vimta.com Contact:Keerthana9160712930

QC Executive (Bioanalytical)-Vimta Labs, Hyderabad Experience: 1-3 years in relevant industry CTC: 3 LPA Responsibilities: <ol><li>Responsible for monitoring the compliance of all bioanalytical SOPs.</li><li>Prepare/Review of Validation &amp; Study Protocols, Method STPs &amp; Method Validation Reports,&nbsp;bioanalytical reports and related analytical master files and chromatographic raw data (soft &amp; hard&nbsp;copy).</li><li>Ensuring the calibration status of all bioanalytical equipment and related instruments and the&nbsp;reference standards status.</li><li>Review of Qualification and Calibration records of all equipment.</li><li>Verification of logbooks and temperature recordings of freezers on a regular basis.</li><li>Ensure the archival of all completed study and validated documents.</li><li>Review of Audit Trails and back up data.</li><li>Preparation of responses for QA observations and to take necessary corrective action.</li><li>Provide Training on bioanalytical SOPs and guidelines to bioanalytical team as necessary.</li><li>Responsible for Initiation/Review of all QMS documentation such as change controls, deviations and CAPA.</li><li>Responsible to face Regulatory Inspection and Sponsor audits.</li><li>Responsible for Initiation/Review of all QMS documentation such as change controls &amp; deviations, CAPA.</li></ol>&nbsp;

Medical Monitor @ Vimta Labs, Hyderabad Experience: 3-6 years Qualification: MBBS / MD with relevant experience. CTC: 7-15 LPA Responsibilities:<ul><li> act as medical monitor and interact with site investigators for patients eligibility and SAE documentation and follow up. Coordination with regulatory, ethics committee and sponsor for submission of AE/SAE data. </li><li> Collaborates with clinicians, site investigators, clinical scientists, biostatisticians, to interpret protocol and study results and ensure study results and statistical interpretations are accurately and clearly reflected in relevant documents </li><li> Handle sponsor, regulatory and ethics committee queries related to eligibility, AE documentation and PV. </li><li> Creates and maintains standard operating procedures and work instructions for preparation and maintenance of compliant medical monitoring documents </li><li> Participates in scientific communication planning, including development of strategic medical monitoring/ communication plans </li></ul>Review and edits protocols, regulatory documents, ICFs, CRF/eCRFs and various relevant study plans for efficacy and safety summaries. Review of related clinical documents, such as abstracts, posters, presentations, and manuscripts for Clinical Trial/PK PD study design for biosimilars.<ul><li> Therapeutic area training of clinical operation team and medical input to DM and statistician team </li></ul> Interested candidates can share their resumes to keerthana.rojanala@vimta.com Contact:Keerthana9160712930

Sales Manager - EMI/EMC @ Vimta Labs, Shameerpet Sales Manager EMI/EMC Test Facility : Sales Managers' primary responsibility is to sell an organization's services and products, perpetually finding unique ways to engage and increase audience size and clients. The Sales Manager might be responsible for managing clients at a local and regional geography. Experience required: 3-8 years with any leading regulatory service provider company serving electrical industry for testing and certification for India &amp; Global Market. <ul><li>Excellent communication and presentation skills, self-motivation </li><li>Build and maintaining client relations</li><li>Work with internal departments such as the Marketing and operations teams to engage audiences and clients more deeply</li><li>Meet and exceed KPIs and sales targets </li><li>Possess deep knowledge of business product offering and value proposition, </li><li>Must have experience in working with ESDM, home appliances, Medical device, IT/AV, Defense sector, etc.</li><li>Follow organizational policies and regulations that affect the Sales department</li><li>Proactively pursue new business and sales opportunities</li><li>Solve problems for clients and customers by developing innovative and tailored sales solutions</li><li>Be a brand ambassador and reflect company values at all times</li><li>Extremely strong verbal and written communication skills</li><li>High-level proficiency with MS Office programs</li><li>Capacity to work independently</li><li>Passion and drive</li><li>Competitive spirit</li><li>Professionalism</li></ul> Interested candidates can share their resumes to keerthana.rojanala@vimta.com Contact:Keerthana9160712930