Qualification & Experience Educational Qualification Bachelors/ Masters in biomedical sciences/ biomedical engineering Skills required: Knowledge on imaging techniques ( PET CT scan, MRI scan, etc). Should be able to interpret the imaging studies Good analytical skills Good English language skills (oral and written) Knowledge of MS office

Qualification & Experience Experience : Minimum 1 YearEducation : Bsc NursingWe are seeking a compassionate and skilled Registered Nurse to join our Emergency Department team. The ideal candidate will have experience in emergency care, excellent clinical skills, and the ability to work in a fast-paced environment.

Qualification & Experience Experience : 2- 5 yearsEducation : Bsc, GnmThe General Medicine Staff Nurse provides high-quality patient care in the general medicine department, assisting physicians, monitoring patients, and ensuring effective care plans. The role requires a compassionate and detail-oriented professional capable of working in a fast-paced healthcare environment.

Qualification & Experience Experience : 1yearEducation : B Pharm , D Pharm , Pharm D, Pharmacy assistantWe are seeking A hard-working,skilled pharmacist to join our pharmacy Department team. The ideal candidate will have experience in managing pharmacy , excellent clinical skills, and will have ability to work in a fast-paced environment

ResponsibilitiesObstetrics and gynaecology (O&G) care for pregnant women and unborn children, and look after women's sexual and reproductive health.Qualification & ExperienceWork Experience : 1-3 Yrs. Qualification : MS/DNB-Obs. & Gyn.

Qualification & ExperienceWork Experience : Minimum 1 year Qualification : Diploma in Operation Theater Technician Description : Experience in assisting Transplant, Neuro Surgery, Laparoscopy, Endoscopy, Cardiac etc.. Good Communication Skills & Team spirit

ResponsibilitiesHandles the sourcing, negotiation, and procurement of medical supplies, equipment, and services. Key roles, such as Purchasing Managers or Officers, ensure cost-effective, timely acquisition of quality products while maintaining inventory levels to support clinical operations.Qualification & ExperienceWork Experience : 1 - 5 Qualification : Any Graduate

Responsibilities  Hands-on data scientist or machine learning engineer that will be expected to ideate, design, develop, model and deploy advanced solutions  Collaborate with stakeholders to define project objectives, formulate data-driven hypotheses and identify KPIs for analysis  Gather, preprocess and explore large-scale structured and unstructured data from diverse sources, including clinical trials, patient records and genetic data  Apply advanced statistical analysis, machine learning algorithms, and predictive modelling techniques to extract insights and develop models that drive actionable recommendations  Conduct exploratory data analysis (EDA) to identify patterns and anomalies in the data and propose solutions to business problems  Develop and implement predictive models (e.g., regression, clustering, time series forecasting) and generative models (e.g. LLMs) to solve complex business challenges  Collaborate with data engineers and IT teams to ensure data availability, quality and reliability for analysis and modeling  Create and present complex analytical findings and insights to both technical and non-technical stakeholders through clear and compelling visualizations, reports and presentations  Stay up-to-date with the latest methodologies and best practices in statistical analysis, machine learning, and the biopharma industry.Qualification & ExperienceWe welcome a master's or Ph.D. in a relevant fields such as Data Science, Statistics, Computer Science or a related discipline. Proven experience (typically 5+ years) in a data science role, preferably within the biopharma or pharmaceutical industry Strong background in statistical analysis, machine learning and predictive modelling techniques Experience in handling and analyzing large-scale structured and unstructured data sets using SQL, NoSQL or similar technologies Demonstrated ability to develop and implement predictive models and machine learning algorithms Experience working with healthcare data, clinical trials, or related domains is highly desirable Solid understanding of the biopharma industry, including regulatory requirements, clinical trial design, and healthcare data sources

Responsibilities  Good knowledge of ANDA submission activities and post-approval procedures and related ICH and USFDA guidelines.  API DMF and DMF Change Notification review with respect to USFDA regulatory requirement.  Exposure of the Solid oral dosage form / Sterile dosage form / complex dosage form / topical-Inhalation dosage form and brief manufacturing process and key regulatory aspects.  Ability to preliminary review the change cases with respect to ICH quality / post approval USFDA guidance and aware for Post approval submission guideline and procedure for Annual report/CBE 0/CBE 30 and PAS filling  Drafting of the Annual Report with required submission data as per USFDA guidance.  Preliminary review of entire submission package.  Drafting the controlled correspondence/Briefing Package to FDA on specific cases as needed for assigned projects.  Awareness about the FDA recommendation on the commercial marketing status notification submission in terms of content and time frames.  Coordination with Cross Functional teams for the documents availability as per regulatory submission plan.  Ensure the no delay in drafting and compiling the regulatory submission.  Maintain regulatory information as per allocated task. Qualification & ExperienceB. Pharm B. Pharm - Required M. Pharm M. Pharm - Preferred Experience: 5 years or more in 5 - 8 Years

ResponsibilitiesResponsible for review of URS, DQ and vendor/ supplier’s documents related to qualification. Responsible for preparation and review of Validation/ Qualification protocol and report. Responsible for execution and review of Qualification / Re-Qualification and Validation activity of Equipment / System / Facility and Plant utilities. Responsible to co-ordinate with manufacturing, Engineering and QC personnel for respective Qualification / Validation / Re-qualification activity for timely completion of activities. Responsible for preparation and review of media fill and hold time protocol and report. Responsible for preparation of Standard Operating Procedures of Quality Assurance Department. Responsible for assessment of Change Control, Deviation, CAPA, Investigation etc. Responsible to prepare protocols of process validation and cleaning verification/validation. Responsible to conduct sampling activity as per the protocols (Process validation and clearing validation etc.). Responsible for preparation, review and execution of risk assessment activity related to equipment/ process/ facility/ system. Responsible for preparation and updation of Annual Validation Planner. Responsible for review of the master and executed documents of cross functional team (CFT). Responsible for review of master batch documents. Responsible to review the different type planner and calibration certificates. Responsible to monitor cGMP compliance at shop floor. Activities other than defined in the Job responsibility are to be done, as per the requirement of HOD, by following HOD’s instruction and guidance.Qualification & ExperienceQualification: M.Sc / B.Pharm / M.Pharm Experience: 2-5 years Requires experience in Validation for Injectables plant with experience of working in regulated industry including US and/or Europe markets.