Pharmacovigilance Job Vacancies in Maharashtra

Review medical records and translate them into standardized codes using ICD-10, CPT, and HCPCS coding systems. Collaborate with healthcare providers to obtain accurate information for coding purposes. Ensure all codes are compliant with healthcare regulations and insurance requirements. Assist in maintaining accurate documentation and coding practices to meet healthcare standards. Communicate with the coding and billing departments to resolve discrepancies or issues. Stay updated with changes in medical coding practices and healthcare regulations. Educational Background: Nursing degree (RN, LPN, or related nursing qualifications). Certification (Preferred, but not required): Certification in Medical Coding (e.g., CPC, CCS) or willingness to pursue certification after employment. Technical Skills: Basic knowledge of medical terminology, anatomy.Why Join Us? Training & Development: Comprehensive Medical Coding training will be provided to help you gain expertise in medical coding. Career Growth: We offer opportunities for career advancement and professional development within the healthcare industry. Work-Life Balance: Flexible working hours and a supportive environment. Competitive Compensation & Benefits: Health insurance, paid time off, and other benefitsQualificationsPharmacy : B.Pharmacy / M.Pharmacy / Pharmd Life Sciences : Microbiology,Biotechnology Biochemistry Botany zoology chemistry BioInformatics Medical : MBBS BDSParamedical : BHMS BAMS GNM ANM Nursing MLT Food and Nutrition

Job Description: - Should have knowledge about Adverse Events (AE), PV and Quality check. Adverse Event reporting and its source data collection and Verification Adverse Event reconciliation Listening of sample calls and verifying with respect to AE reporting. Review of sample calls of FC, PTC Interaction summary with respect to AE reporting. Sample Audit of Rx with respect to AE reporting. Preparing report basics all Audit parameters and sharing with HCAH Management & Client Custodian of Adverse Event SOP and Tracker Conducting Process training and Pharmacovigilance / Adverse Event Reporting Should be responsible for checking all AEs, AE tracker, Zelthy hygiene check and Coordination with PV team. Should be responsible for doing Call quality, Documents check and PV check.

Responsibilities Support to manufacturing for achieving performance targets. Lead the technology input into the root cause analysis of complex process/engineering issues. Define improvements and upgrades in existing processes / equipment / technologies to reach higher capacities, higher process efficiencies. Identify, justify and prioritize plant improvements for PIOs, CAPEX, REVAMP projects, including major projects (new plants) and support:- Review process-engineering documents as part of Basic Engineering and Detail Engineering.- Evaluation of external technologies for improvement schemes as well as for new plants- Review of Process Design Package of Technology Licensors- Preparation of Design Basis documents and Process Design Packages for in-house developed / conceptualized improvement schemes- Participation in PHA reviews (HAZID / HAZOP)- Evaluation of vendor technical proposals including cost-benefit analysis - Review of vendor documents post order.- Preparation / review of Operation Manuals, SOPs and SOCs. Catalyst / chemicals / additives / fuels evaluation. Audit and benchmark plant/ product / energy performance. Ensure achievement of set milestones for pilot / scale up studied. Anticipate constraints / trends in technology and product application range and review and recommend alternatives for implementation. Participate in commercial plant trial. Develop, validate, customize & maintain simulation / APC models. Preparation of final technology comparison reports. Participate in PSM activities. To coach/mentor and support the on-boarding and development of the GETs (technology)Skills: Has a thorough knowledge of chemical engineering, codes, and standards, and of process technology in respective domain. Works independently, takes independent actions on technical issues within the field of expertise. Relevant industrial experience (4-8 years) with good technical background and good communication skills.

Job Description Reviewing and giving medical opinion on various reportsoriginating from literature Reviewing literature references for signal detection andaggregate reports Writing medical comments Contributing to creating search strategiesQualifications Medical University degree (Doctor of medicine) Advanced level of English C1 Good IT skills (MS Office) Good baseline knowledge of scientific literature retrievaland valuation (mainly using PubMed and EMBASE) People who are excited to learn and contribute to patientsafety Excellent organization skills with attention to detail Excellent interpersonal and communication skills