Responsibilities Develop, implement, and manage operational excellence strategies and programs aligned with company goals and objectives.  Identify opportunities for process improvement, waste reduction, and cost optimization through data analysis, process mapping, and root cause analysis.  Lead and facilitate Lean, Six Sigma, and other continuous improvement projects from conception to completion, ensuring measurable outcomes.  Train, mentor, and coach employees at all levels on operational excellence methodologies and tools.  Establish and monitor key performance indicators (KPIs) to track progress and success of improvement initiatives.  Collaborate with cross-functional teams (e.g., Manufacturing, Quality, Supply Chain, R&D) to ensure successful implementation of process changes.  Document best practices, standard operating procedures (SOPs), and process flows.  Drive a culture of continuous improvement, problem-solving, and accountability within the organization.  Prepare and present reports on operational excellence activities, achievements, and future plans to senior management.  Stay abreast of industry best practices and emerging trends in operational excellence.Qualification & Experience Bachelor's degree in Engineering, Operations Management, Business Administration, or a related field. Master's degree preferred.  Minimum of 8-10 years of experience in operational excellence, continuous improvement, or a related role within the pharmaceutical or manufacturing industry.  Certified Lean Six Sigma Black Belt or Master Black Belt strongly preferred.  Proven track record of successfully leading and implementing significant operational improvement projects with tangible results.

ResponsibilitiesLiterature study for applications of specific product and data compilation. To perform lab trials related to food/premix applications and conduct stability study. Preparation of premixes as per requirements received from marketing team and to send for analysis and to customer for trial purpose. New product designing including calculations for label claims and respective sources, nutritional values and related aspects. To perform calibration of lab instruments and equipment’s. Maintain documents of lab trials, analytical reports, samples dispatched, marketing queries, audits and routine work requirements. To follow up and review of pending analysis samples and documents. Procurement of new raw materials as per requirement. To ensure compliance of safety measures. Imparting and organizing the internal training activities for HNH and ANH department concern people. To ensure compliance to audits. To ensure avoidance of breach of data integrity. Responsibility of the producing quality products & maintaining quality.

Responsibilities Under general supervision of lab team leader, independently perform routine scientific research tasks using standard techniques, procedures and equipment.  Adapt and optimize or develop new methods and procedures, actively contribute to technical solution finding process.  Propose solutions and discuss with manager  Show engineering and tech transfer proficiency  Assist and support to R & D team and cross functional team in scale-up of new products technology  Troubleshoot & or improve existing processes  Summarize and document results in lab journal, prepare technical reports.  Maintain clean working laboratory environment and suitable working equipment.  Perform general lab assignments (e.g. raw material inventory review, lab instruments ) as assigned. Comply with regulations concerning safety, health and environment.  Under general supervision of lab team leader, independently perform routine scientific research tasks using standard techniques, procedures and equipment.  Adapt and optimize or develop new methods and procedures, actively contribute to technical solution finding process.  Propose solutions and discuss with manager  Show engineering and tech transfer proficiency  Assist and support to R & D team and cross functional team in scale-up of new products technology  Troubleshoot & or improve existing processes  Summarize and document results in lab journal, prepare technical reports.  Maintain clean working laboratory environment and suitable working equipment.  Perform general lab assignments (e.g. raw material inventory review, lab instruments ) as assigned.  Comply with regulations concerning safety, health and environment.

Responsibilities Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned To be well disciplined & maintain the same in the production department. To maintain the safety and housekeeping practices at work place. To ensure and follow good and online documentation practices. To ensure proper labeling procedure wherever applicable as per procedure. To ensure that cleaning the area as per related SOP ‘s are conducted and maintained as per proper cleanliness. To ensure the Calibration/Preventive maintenance of the equipment as per the schedule. To maintain and ensure cleaning and operation activities are performed as per procedure. To maintain the batch as per instruction given in batch document / procedure. To ensure material movement is conducted as per procedure. To ensure training of our self on current version of procedure prior to perform activity. To perform the activities assigned to him by the concerned section seniors or by his superiors in area. To follow the cGMP practices. To showcase the value of collobaration with own/other departments to complete the work assigned. To escalate immediately to concerned superior / manager for any deviation / non-compliance /abnormal observation. Shall always be ready to accept new challenges & multifunctional activities. Shall always stick to the time line provided or assignment given by superiors, to avoid any delays and any non-compliance. Works as a member of a team to achieve all outcomes. Performs all work in accordance with all established regulatory and compliance and safety requirements.Qualification & ExpeirneceB.Pharm Knowledge, Skills and Abilities Adequate knowledge and ability in handling /supervising the manufacturing activities In depth knowledge of cGMP practices Identify and escalate equipment related issues. Experience 5 years 0 months

ResponsibilitiesDevelop, edit, format, and maintain R&D documentation including but not limited to: Design History Files (DHF) Standard Operating Procedures (SOPs) Protocols, Reports, and Technical Files Risk Management Documents (FMEA, ISO 14971 files) Design Control documentation Ensure documents are accurate, consistent, clear, and compliant with regulatory and quality standards.Qualification & ExperienceBachelor’s degree in Life Sciences, Pharmacy, Engineering, or a related field. 3–7 years of experience in documentation within Pharmaceutical or Medical Device R&D. Strong understanding of regulated documentation practices and quality systems. Experience working in compliance with FDA, ISO, and ICH guidelines. Proficiency with EDMS tools 

ResponsibilitiesSupport management of all analytical activities related to projects within in responsibility of AS&T group Support Life-cycle management of analytical methods, including control of method performance, analytical method improvements, pharmacopoeia and health authority compliance (support subject matter expert in health authority inspections) Single point of contact for internal and external clients and contract laboratories, if applicable. Support timely analytical implementation (Method Transfer and Method Validation) for (new) projects in the course of product transfers Setup and monitoring of stability studies Support overarching product investigations cross functional, e.g. QC, QA, Production, MS&T Support implementation of GMP requirements. Support compilation and review of documents (analytical protocols and reports, annual performance quality reports, ongoing process verification reports, registration documents)Qualification & ExpeirneceEducation: M.Pharm/ Engineering/MSc/M.Tech/equivalent from a reputed institute. Experience: Minimum 5 years’ experience in Quality Assurance, Quality Control, Regulatory or in the manufacturing of pharmaceutical drug substances or products/ medical device/ expertise in Learning management system Problem Solving skills and stakeholder management.

Responsibilities Serve as the primary liaison between Novartis and assigned investigational sites Conduct Site Initiation, routine monitoring (on?site and remote), and Close?Out visits as per Monitoring Plan Ensure compliance with protocol, ICH/GCP, regulatory requirements, and Novartis SOPs Proactively identify site risks, issues, and deviations; drive timely mitigation and resolution Build strong site partnerships to optimize patient recruitment, flow, and site performance Ensure accuracy, completeness, and timeliness of site documentation and sTMF Support audit and inspection readiness and implement CAPAs within agreed timelines Collaborate cross?functionally with CPMs, CRA Managers, Medical, MSLs, and other stakeholdersQualification & ExpeirenceDegree in a scientific or healthcare discipline (or equivalent relevant experience). Minimum 4 years of pharmaceutical or clinical research experience Hands?on experience in site monitoring and clinical trial execution Strong knowledge of ICH/GCP, regulatory requirements, and clinical trial processes Ability to manage sites independently with strong decision?making capability

ResponsibilitiesCoordination and management of analytical method transfers and stability studies. Compilation of data reports Life-cycle management of analytical methods, including control of method performance, pharmacopoeia and health authority compliance and definition of method improvements. Handling of deviations, investigation, OOS/OOE/OOT cases as well as changes and complaints Work on various Labware LIMS workflows including various modules like Lot management, stability management, instrument interfacing, reagent management. Management of Master data in Labware LIMS and perform migration of LIMS records. Execute validation of configured workflows and calculations relevant to LIMS modules Perform test run/dry run in Labware LIMS for various workflows. SAP master data management: Maintenance of master data, creation of Q-info records and other SAP related activities. Collect, transcribe and/or compile data from various repositories (SAP, LIMS, external COAs) Trend and report all QMS elements as per the request Monitor, trend and report Health Safety and Environmental parameters Implementation of GMP requirements. Compilation and Review of documents (analytical protocols and reports, annual performance quality reports, ongoing process verification reports, registration documents (Common Technical Document modules). Perform activities of a Quality Control expert as defined by the respective sit and support regulatory requirements – routine queries, Chromatogram requests Create and review GxP documents including SOPs, working procedures, trend reports, qualification reports and technical investigations, as and when needed Qualification & ExpeirnecePharmacy/ Science/ MBA / M.Tech/MSc /Engineering/ equivalent from a reputed institute Min 6 years of experience in Quality Assurance, Regulatory or in the manufacturing of pharmaceutical drug substances/ products/ medical devices GxP knowledge, Basic IT knowledge

ResponsibilitiesDirectly supports electronic submission of regulatory documents / applications including IND, CTA, NDA, BLA, MAA, etc. through formatting, processing, and compilation of Word and PDF documents to the appropriate client specifications. Formats and reviews Word documents in preparation for publishing, in accordance with all relevant client style guides and / or regulatory guidelines and specifications and within all established timelines. Performs document conversion to PDF, and formats and reviews PDF documents to specification (for eCTD compliance), including bookmarks, hyperlinks, keyword linking, document properties, etc., in accordance with all relevant client style guides and / or regulatory guidelines and specifications and within all established timelines. Compiles regulatory documents / reports, gathering all required documents, within all established timelines. Publishes regulatory documents according to all relevant guidelines and specifications for eCTD submission, performing all relevant pre- and post-publishing quality review checks. Prepares and transfers final documents for publishing, supporting client and internal team during submission preparation, routing documents for review and approval, where applicable. Adheres to established regulatory standards / guidelines including but not limited to: ICH E3 / E6(R2) / M4, EU MDR / IVDR, Company standard operating procedures, and client standards instructions. Supports multiple publishing activities / projects simultaneously and manages own workload, ensuring completion of all projects within established timelines, immediately escalating any issues.Qualification & ExpeirenceMinimum 3 years of experience in document publishing and / or formatting. Pharmaceutical / biotech industry experience (specifically, INDs / CTAs, NDAs / BLAs / MAAs) preferred. Other professional and/or educational experience may contribute toward these minimum requirements, as determined on a case-by-case basis.

ResponsibilitiesGeneral Responsibility Adhere and comply with Organization Regulations and Administrative Policies. Adhere and comply with policies and procedure related to patient care, infection control, patient safety and accreditation standard. Care Delivery Demonstrate clinical competence in all aspects of patient care. Evaluate the quality and appropriateness of care and assess the impact of nursing intervention as appropriate. Assessment and reassessment of pain and management of pain Ensure compliance with all policy and procedure for medication management. Explain plan of care to patient and family. Document and handover all patients records as per policies and standards. Educate patient and family as required Ensure the involvement of the patient, family and significant others in the patient's care. Ensure plan of care is implemented. Demonstrates correct use and assembly of required equipments, instruments and appropriate cleaning of the same. Quality Management Understanding of clinical and other established performance indicators to ensure ongoing quality Improvement. Follow international patient safety goals. Report all near miss, sentinel events and any other incidents. Identify and escalate any life threatening issues, associated procedures, protocols and policy guidelines. Always maintain privacy and confidentiality of patient information and records. Comply with all quality standards as decided by organization for patient safety and quality of care Training and Development Participate and contribute in scheduled in service training programs like ACLS, BLS,PALS,NALS(If applicable), CNEs, conferences etc., Functional Area Responsibility Perform Cardio vascular assessment. Understand and demonstrate infection control guidelines, practices and bio medical waste management Handle cardiac monitors. Assess and interpret Intra Cranial Pressure and Glasgow Coma Scale. Haematoma management and post op care. Nursing management of patients on ventilator. Manage IV fluid calculations and drug calculations. Ability to take Care of Intravenous lines and Central lines, Perform Endotracheal and oral suctioning. Ability to position patients appropriately Knowledge about the different types of sterilisation and aseptic techniques followed in NH. Awareness on DVT prophylaxis and FAST HUG protocols. Assisting for pace maker insertion and assisting Different modes of Oxygenation. Interpret Arterial Blood Gas values. Thrombophlebitis and Nursing management. Perform drainage,ROMOVAC drain monitoring and intake and output documentation.  Storage, administration and disposal of Narcotics. Processing patient samples for ABG, VBG, GRBS, CARDIAC SOB ,ACT & PT INR on POCT devices. Performs Allen’s test, draws arterial blood and perform Arterial Blood Gas and Venous Blood Gas analysis for Patient samples. Monitors and update the critical value reporting documents for all POCT reports. Informing panic value to treating consultants and document the same. Qualification & Experience       Education: Diploma / Bachelor’s degree in nursing Registration: Valid registration in the state Nursing Council from where B.Sc. Nursing / GNM was completed. Experience: Freshers / candidates with 1 or 2 years of experience Knowledge & Skills Required: Knowledge of nursing principles, techniques and procedures for the delivery of effective patient care. Good communication & interpersonal skills. Be proactive, punctual and empathetic N.B – The above also includes any other job assigned from time to time.I do hereby declare that the Job Responsibilities are properly explained to me during Induction/ Appraisal/ Redesignation and understood by me. I will try to deliver the best by meeting the mentioned standards.