Qualification & ExperienceDesignation: Senior Echo cardiography TechnicianQualification: UG,Diploma, Other GraduateKey skills: Perform and assist in Echo cardiography (2D, Doppler) Conduct DSE (Dobutamine Stress Echo) procedures Record and interpret ECG and TMT (Treadmill Test)Interested candidates meeting the above criteria are encouraged to submit their resume to [email protected] or via WhatsApp at +91 63968 52016 .

Qualification & ExperienceDesignation: PharmassistQualification: B.PharmaKey skills: Key pharmacist skills focus on combining deep pharmaceutical knowledge with patient-centered care and operational efficiency.Interested candidates meeting the above criteria are encouraged to submit their resume to [email protected] or via WhatsApp at +91 63968 52016 .

Qualification & ExperienceHospital Management Eligiblity:- Under Graduate, Graduate, Diploma, PG ,Other Graduate. Experience in Hospital Industry is required.Interested candidates meeting the above criteria are encouraged to submit their resume to [email protected] or via WhatsApp at +91 63968 52016 .

Qualification & ExperienceWork Experience : 0-4 Years                 Qualification : B.Pharm/D.Pharm       Description : Health care Experience will be Preferrable and Knowledge        

ResponsibilitiesPiramal Pharma Limited is seeking an Executive, Quality Assurance to ensure the highest standards of product quality and compliance with regulatory requirements. This role involves active participation in quality systems, documentation, and operational oversight within our manufacturing facilities. Preparation of APQR, review of documents and records. Supporting to Customer complaint & assistance in implementation of CAPA. To assist in maintaining Food safety & Quality management system. To review HACCP verification & validation plan, adhere to FSSAI requirements for the food premixes division and comply with the requirements of various regulatory authorities and customers. To review SOPs, batch manufacturing and packing records, specifications and test methods of the products. Handling of deviations, change controls, out of specifications may occur at all stages of storage, dispensing, manufacturing, packing, testing and distribution. To ensure issuance, control, distribution, storage, retention and destruction of quality documents and corporate guidelines as per Food safety & Quality management system. To assist in compliance to the current ISO 9001, D&C Act, FSS Act 2006, FSSC 22000, FAMI-QS, WHO-GMP, UNICEF and other customer and regulatory requirements. Reporting of daily non-conformance, online deviation if any. Preparation and updation of Q.A departmental SOP’s and loading it in DCS (Document Control System) ENSUR , Change control in trackwise and handling of SAP system.

ResponsibilitiesSenior Research Associate - R&DSenior Research Associate - R&D Design the scheme of experiments. Plant trouble shooting, investigation and root cause analysis. IUT support for vendor qualification and plant batches. Carry out experiments during the feasibility and optimization stage. Visualize the development needs of the product. Understand the safety and environmental aspect. Solve the problems and queries related to the development of the product and discuss them with the Group Leader / HOD. Familiarize with the problems faced during scale-up and identifying all critical process parameters for a seamless scale-up Knowledge on IUT, VQ, LFR/PDR reports documentation. Understand the scalability of the chosen process, in coordination with TSD and Production. Amicable relationship with PRD and ARD and work planning accordingly Keep the Group Leader well informed about the experiments and their results by maintaining the lab journal/ documents well.

ResponsibilitiesPlanning of analysis in wet and GC to meet the dispatch requirements as per the customer requirements.  Coordinating with Quality Assurance department in releasing the products.  Timely intimation of the sampling requests with proper documents.  Providing the technical support related to IT where ever required.  Sampling of all materials.  Preparation of packing material specifications and loading in SAP.  Wet analysis of all materials wet parameters.- Planning of analysis in wet and GC to meet the dispatch requirements as per the customer requirements. - Coordinating with Quality Assurance department in releasing the products. - Timely intimation of the sampling requests with proper documents. - Providing the technical support related to IT where ever required. - Sampling of all materials. - Preparation of packing material specifications and loading in SAP. - Wet analysis of all materials wet parameters. MSC Chemistry

Responsibilities Focus on building trustful relationships with TLs and HCPs not covered by field based MSLs, increasing the medical reach and coverage of new specialties /TLs from tier 2 and 3 cities where current field-based MSLs are not reaching out, communicating scientific information about our products and gathering insights to support our decision-making process.  Partnering with internal stakeholders, mainly field based MSL, KAM (Key account manager) and First Line Sales managers (FLSM), the DMSL identifies external customer scientific and educational needs. With an innovation mindset, the DMSL analyzes these insights and proposes content and the channel through which to be delivered, liaising with cross-functional team members (MSL, MA, Clinical operations, BU, amongst others) to create and deliver it.  The DMSL will exchange and disseminate scientific and educational related information with HCPs, engaging with them as a subject matter expert via various innovative TL engagements tactics and formats (both proactive discussions on-label, and reactive discussions for unsolicited off-label questions in alignment with local regulations).  Customer facing will take place via remote channels mainly, with occasional face to face interactions on-need basis.  Responsible for supporting clinical trial team on subjects related to interventional clinical trials. Support with data collection, feasibility & initiation visits.  Responsible for documenting and process medical information queries in alignment with MI handling procedures.  Prepares reports and tracking activities: The DMSL submits timely reports of HCP interactions and events, as well as tracks activities against agreed upon Performance & Development objectives. Qualification & Experience Bachelor’s degree in medicine, natural sciences, or pharmacology. Advanced degree in science-related field eg. MD, MDS, PharmD, PhD preferred.  2-3 year of experience in the pharmaceutical industry as an MSL preferred or experience in drug information, clinical research and development, or other clinical relevant activities.  Preferably experienced in Cardiovascular and Chronic Kidney Disease in Type 2 Diabetes areas.  Innovation and experimentation mindset and creativity, capitalizing on new technologies.  Digital savviness. Experience in digital content creation preferred. Pragmatic manner, adapting quickly to changing environments. 

Responsibilities Exchange and dissemination of scientific, educational, and research related information:  The MSL plans, prepares and engages with Thought Leaders (TLs – Doctors) as an information scientist and colleague both proactively and reactively via various innovative TL engagements tactics and formats. MSLs provide dissemination, clarification and education of scientific data, study protocols, meeting abstracts, and professional literature (both proactive discussions on-label, and reactive discussions for unsolicited off-label questions in alignment with local regulations). Interactions with Medical Societies and Advisory Boards:  The MSL answers medical / scientific queries of Medical Societies with regards to Bayer products and organizes / supports / participates in advisory boards.  Participation at / networking in Congresses and Conventions:  The MSL attends congresses and conventions, interacts with TLs (Doctors), establishes new contacts and gathers competitive intelligence.  Coordination of Scientific Education Activities:  The MSL plans and organizes scientific training and education events / sessions with TLs within their specific therapeutic area or product. TL identification / profiling / segmentation and strategy and engagement planning:  In alignment with product Medical Affairs plan, the MSL contributes to internal understanding of specific TL interests and expertise within the medical community at large. Preparation of reports and tracking activities:  The MSL submits timely reports and tracks activities against agreed objectives Secondary Activities:  External scientific support, training and education: The MSL provides additional external scientific support, training & education not covered by other primary activities Qualification & Experience Qualification in natural sciences, or Medical background (MD/ MBBS/BAMS/ BDS/ MDS)  Basic knowledge of the concerned therapy area (Diabet,CKD,Heart failure) and related molecules  Basic understanding of clinical trials, their design, and rationale 

ResponsibilitiesPublish and dispatch major and complex routine/lifecycle management eCTD submission projects for EU, US and Canada. Exposure in handling post approval submissions publishing and transmitting quality submissions to agency. Perform document level publishing activities, troubleshoot document issues and perform quality control checks for submission ready documents as per the agency guidance. Collaborate with scientific personnel for planning, preparation and publishing Maintain working knowledge of internal and external publishing standards. Basic knowledge of ICH and eCTD related specification/guidelines governing regulatory submissions (eCTD, NeeS, paper) Must be aware of technical systems like Global Insight, Veeva Vault, ISI Toolbox, Adobe Acrobat, Lorenz ValidatorQualification & ExperienceB. Pharm: Minimum 2 years experience in Regulatory Affairs M. Pharm/ Master of Life Sciences: 0-1 year of experience in Regulatory Affairs Command over spoken and written English Sensitivity to the cultural diversity of a global organization Good understanding of regulatory IT systems