Qualification & Experience                              Experience Required : 5 + years of experience in NABL Accredited hospital Laboratory experience                         Qualification Required : MBBS, MD (Pathology)              

ResponsibilitiesProvide clinical support and guidance to doctors, nurses, and hospital staff on product usage. Conduct product demonstrations and in-service training at hospitals and healthcare facilities. Assist in clinical evaluations, trials, and product adoption. Build strong relationships with key stakeholders, including surgeons, nursing staff, and hospital management. Ensure proper usage protocols and compliance with clinical standards. Support the sales team with clinical insights and product positioning. Handle queries, troubleshooting, and post-application support. Maintain accurate records of hospital visits, training sessions, and feedback. Stay updated with clinical knowledge, industry trends, and product developments. Qualification & ExperienceB.Sc. Nursing / GNM Experience: 2–5 years of clinical experience (hospital/ICU/OT exposure preferred). Strong understanding of clinical procedures and patient care. Good communication and presentation skills. Willingness to travel extensively within the assigned region. Ability to work independently and manage multiple hospital accounts. Experience in wound care, critical care, or surgical assistance

Qualification & ExperienceExperience: 1–6 Years Education: B.Tech / M.Sc

Qualification & ExperienceDM/DNB Gastroenterology With 2-10 years experience

Qualification & ExperienceDM/DNB Endocrinology With 2-10 years experience

Responsibilities Safety Physican Role : Responsible for the preparation/ review of safety aspect in clinical documents,clinical study concepts, clinical study protocols, Investigator’s Brochures, clinical study reports, clinical modules of CTD, response documents for EC, MoH on the program. Take on role of safety physician for global clinical studies/programs. Responsible for the medical oversight during trials and functions as SME for scientific and medical questions during the trials. Review of safety review plan, SAE reconciliation, safety listings and coding during the trials/programs Primary study contact for sites’ personnel and project team in the event of medical-scientific questions Collaboration with the other members of the Pharmacovigilance team to process Serious Adverse Events for the clinical trials to which is assigned as CRP Review of CROs-Medical assessment of adverse event reports, detecting and assessing risks and proposing risk mitigating activities Case Narratives review, Coding of medical terms Participating in Risk management activities like protocol modifications due to safety or efficacy concerns, restrictions in study population or indications, changes to the informed consent document relating to safety issues, newsletters to investigators Input in development of Safety Update Reports (PSUR and DSURs) and as necessaryQualification & ExperienceMD or MBBS Minimum Experience/Training Required : At least 5-7 years of experience in pharmaceutical industry with minimum of 3 years in relevant clinical development. Ability to lead clinical programs and to run teams in multi-cultural environment at different sites. Expert knowledge of clinical trial methodology, oversight/evaluation of safety and regulatory requirements governing clinical trials. Developmental and Medical Insights of Emerging markets. Works independently, takes responsibility, strong communication silks (written and oral) in English.

Responsibilities Manage site budget template for new studies (multi-country) & budget template updates for protocol amendments under close supervision of budget manager. Manage licensing agreements process for clinical trials tools/outcome questionnaires, including translations as requested by Project Management with oversight. Update budget comparison files for standard & invoiceable items based on site-specific approved budgets in a timely manner to support Site Operations and Project Management finance forecasting needs. Manage HCP agreement related tasks as assigned, including uploading documents within GPAS, FMV assessments, and routing agreements for signatures as requested by the HCP Team CCAs with oversight. Manage assigned routine amendments (such as PI change, site name change) in support of the US/CALA CCA team.Qualification & ExperienceBachelor’s degree Minimum Experience/Training Required :  2–3 years of experience in clinical research, preferably within the pharmaceutical, medical device, or CRO industry  Background in Finance/accounting and excellent Excel/Analytical skills

Responsibilities Understand the market and category opportunities within territory to identify opportunities for market share growth at the customer/account level Maintain deep, current knowledge about medical and nutritional science, the evolving healthcare landscape, and emerging digital trends to support selling and educating a broad and deep network of HCPs about Abbott products Develop and execute on multichannel customer engagement plans that generate demand for Abbott brand product and grow recommendation and market share Leverage information about customer segmentation, type and behaviors to inform customer engagement and account management strategies Develop and maintain strong relationships with HCPs throughout the customer account, at different levels of responsibility and influence using existing relationships with HCPs and others to expand customer network Secure commitment to recommend Abbott products as the brand of choice by increasing HCP knowledge about the role and importance of nutrition on patient quality of life at key points throughout the patient care journey; and the role of Abbott’s products in increasing quality nutrition through consultative selling dialogues Define and deliver ‘Unique Value Proposition’ from the HCP’s perspective (including but not limited to the positioning of Abbott brand products) by continuously uncovering the needs and priorities of individual HCPs using multichannel touchpoints and engagement activities Effectively deliver a consultative sales call from the perspective of the HCP (and their patients) to expand HCP’s knowledge of nutritional interventions and the measurable benefits of Abbott brand products, anticipate and manage objections, and gain clear commitment to recommending Abbott products and other brand-building activitiesQualification & ExperienceMedicine, science, pharmaceuticals/ nutrition Experience MINIMUM WORK EXPERIENCE Experience Details Minimum 1+ years of relevant experience. Minimum of 1 years’ experience in Pharma/Nutrition Industry

ResponsibilitiesHandling of UV visible spectrophotometer, Karl Fischer, Water content determination, Particle Size determination, Titration. and having knowledge of LIMS. Having knowledge about cGMP and good laboratory practices.Qualification & Expeirence M.Sc / B.Pharm Experience 4 years or more. 

ResponsibilitiesTo perform CCIT test of post media fill units. To perform observation of microbial plates exposed in manufacturing area. To perform media fill unit observation as per SOP. Responsible for reporting any OOS, Deviation to In-charge. Responsible for preparation of standard operating procedures of microbiology department. Responsible to co-ordinate with manufacturing, Engineering, and other QC personnel for respective Qualification / Validation / Re-qualification activity for timely completion of activities. Responsible to participate in perform qualification activities of manufacturing and Microbiology area. Responsible for Compressed air /nitrogen gas monitoring and Personnel monitoring Preparation of indents as per the materials/product requirements. To initiate and review of a) Change controls b) Out of specifications c) Deviations. To attain and complete self- training record. Preparation of study protocols with respect to laboratory. Review of instruments logbooks, raw data of raw materials, packing materials, miscellaneous materials, in-process, finished products and water analysis. Preparation of COA. To keep neat and cleanliness at workplace and follow the good laboratory practices and safety related instruction in the laboratory. To perform water analysis and maintain daily water trend. Sampling, testing and release of Raw material, packing material, miscellaneous material samples and in process sample and maintain reserve sample as per SOP. To keep update of instruments logbooks and to record the data in Laboratory Notebook / and respective software. To monitor and plan the activities of various glassware and items required for microbiological analysis with respect to their cleaning, sterilization, and dehydrogenation. To maintain log and status labels for all such items and reconciliation record. Responsible for Pure culture handling and maintenance. To maintain daily logs of area with respect to temperature, humidity, differential pressure, area cleaning, disinfectant preparation, etc.. Responsible to review the environment monitoring, water trends. Responsible to receive the required resources for EM monitoring e.g., plates, samplers, swabs etc.. from microbiology lab and after completion of EM monitoring plates, samplers, swabs etc.. should be handed over to microbiology lab for further process along with applicable formats which is filled in aseptic area. To maintain the Issuance/reconciliation record of items / media for Environment monitoring material e.g., plates, swabs, etc.. Environmental monitoring of manufacturing clean room area as per the defined schedule. Responsible to participate in media fill simulation study. Non-viable particle monitoring of manufacturing clean room area as per the defined schedule. Compressed air /nitrogen gas monitoring and Personnel monitoring. Review of Media fill CD. Qualification & ExpeirenceQualification - B.Sc. /M.Sc.