Responsibilities Lead end-to-end technology transfer of formulations (OSD / semi-solids as applicable).  Plan, review, and approve Technology Transfer Protocols (TTP), Reports (TTR), and risk assessments.  Coordinate transfers from R&D, pilot plant, contract manufacturers, or global sites.  Ensure readiness of manufacturing processes, equipment, and documentation. Process Scale-Up & Validation  Lead scale-up, exhibit, and PPQ batches.  Define and monitor CPPs, CQAs, and control strategies.  Support and review process validation, cleaning validation, and hold time studies.  Drive process optimization and yield improvement initiatives.Experience6–10 years of experience in Technology Transfer, Formulation Development, or Technical Operations within a pharmaceutical formulation company.

ResponsibilitiesPrepare and manage IPQA shift rosters to ensure adequate coverage across all manufacturing and packing areas. Allocate qualified personnel based on activity criticality, workload, and skill matrix. Ensure no gaps during critical operations and maintain backup planning. Ensure IPQA presence during dispensing, granulation, compression, coating, and packing activities to maintain real-time compliance and control. Ensure proper line clearance before starting any activity. Verify equipment cleanliness, status labeling, and removal of previous product/material. Perform and monitor in-process checks such as weight variation, hardness, thickness, disintegration, and coating parameters as per BMR/BPR and SOP requirements. Conduct real-time and final review of batch documents to ensure completeness, accuracy, and compliance with US FDA expectations. Initiate and review deviations, out-of-specification (OOS), and out-of-trend (OOT) events. Drive root cause analysis and ensure effective CAPA implementation.Monitoring of reject handling on shopfloor. Tracking of in-process samples and ensuring timely release of areas for manufacturing and packing. Identification of opportunity of process and practice improvement on shop floor. Ensure all time compliance at manufacturing, packing and warehouse shop floor. Immediate reporting of observed non-compliance to IPQA In charge/ QA Head.Qualification & ExperienceB. Pharm/ M. Pharm/ M.Sc. With relevant experience in pharma. Must have knowledge of working on the shop floor as an in-process quality assurance. Exposure to various regulatory bodies such as US FDA, EU-GMP, MHRA, TGA Exposure to specific dosage forms like OSD.

ResponsibilitiesBe part of the Medicine Department and conduct OPDs on days assigned to you Admit patients under your care in the hospital and manage them independently Take part in any departmental activities for patients Coordinate with senior colleagues and the Director in following the departmental SOPs Maintain meticulous records of patients Ensure that patients are clearly instructed on follow-up visits Attend Departmental meetings and programs Adhere to the hospital guidelines for Associate ConsultantsBe part of the Medicine Department and conduct OPDs on days assigned to you Admit patients under your care in the hospital and manage them independently Take part in any departmental activities for patients Coordinate with senior colleagues and the Director in following the departmental SOPs Maintain meticulous records of patients Ensure that patients are clearly instructed on follow-up visits Attend Departmental meetings and programs Adhere to the hospital guidelines for Associate ConsultantsQualificaation & ExpeirenceMD or DNB in Medicine Experience 5-7 years in a similar role

Qualification & ExperienceQualification:MD/DNB – Emergency Medicine/Anesthesia/General Medicine/Critical CareExperience: 1 year to 7 years

ResponsibilitiesVerification of calibration Validate and dispatch indoor patient’s results Maintains of indents Dispatch EQAS & AIIMS QC result Calibration & validation of cell – counter Observe and act on computer entry Check coagulation controls Look after overall quality of the department Set up new test procedure Check quality control of new lot kit Special coagulation test & special stain Daily indoor reports checking & dispatching Arrange the duties of all the technicians Check annual stock dataQualification & ExperienceB. Sc. (MLT) B. Sc. + D. MLT M. Sc Preferred EXPERIENCE: 8 – 10 years Hospital Experience Preferred Work Experience in Hematology preferred

 ResponsibilitiesDeliver defined operational and documentation activities, managing work independently from initiation through completion, with minimal supervision. Coordinate activities to support self?written supporting documentation, reviewing to ensure alignment with Written Standards and associated governance processes. Review documentation to ensure that it accurately reflects the intent, principles, and requirements of Written Standards, with terminology applied consistently across documents. Support the development, enhancement, and adoption of agile, fit?for?purpose business processes and tools that enable efficient and compliant ways of working. Identify opportunities to improve documentation, tools, or processes, proposing and implementing practical solutions in collaboration with stakeholders. Partner with Training colleagues to support the development and delivery of learning curricula that enable business readiness and effective adoption. Support the Operations & Documentation Lead, contributing to planning, prioritisation, and execution of team activities. Engage with cross?functional colleagues to gather requirements, communicate changes, and support successful implementation of processes and tools. Support audit and inspection readiness activities, including preparation and contribution to corrective and preventative actions where required.Qualification & ExperienceCollege / university degree with 5 years’ experience in regulated industry, pharmaceutical or consumer healthcare business or equivalent experience. Experience developing or maintaining written standards, procedures, or document management. Demonstrated ability to think critically and identify improvement opportunities. Strong written communication skills with attention to detail and accuracy. Confidence working with digital tools and documentation platforms. Ability to work independently, manage priorities, and take ownership of defined deliverables.

ResponsibilitiesDesign and execute new methods and protocols related to area of expertise and/or proactively incorporates new technology and techniques into practice Execute a wide range of experiments/technical studies/tasks Identify and troubleshoot problems in the execution of experimental processes/technical studies/tasks Knowledge of the rationale and hypotheses for experimental designs and/or has extensive theoretical understanding of a particular area of science Develop an understanding of regulatory requirements Actively promote data integrity standards within department Take a leadership role for data integrity projects Assist in new research directions and novel strategies to achieve “project” and department goals Design and execute new methods and protocols related to area of expertise which influence "project" direction Perform complex data management tasks with minimal supervision Interpret results and communicate to supervisor on designs and next logical step of experiments based on the data Keep supervisor informed of progress and activities Independently write specific technical sections of internal and external reports Contribute to scientific papers and internal reports Present at internal Research and Development meetings Begin to develop networking skills through interactions with scientist outside of primary “project” roles Active member of program teams and lead sub-team work Prepare detailed oral or written summaries of results with interpretation for projects/programs Anticipate problems and proactively seeks input from other scientists Qualification & ExpeirenceMaster's Degree from reputed educational institute and relevant discipline (consult manager on equivalent practical work experience in relevant discipline) Experience in Analytical Sciences - NPD

ResponsibilitiesTesting Management: Develop and implement comprehensive testing strategies for Informatica Cloud (IDMC) solutions, focusing on both manual and automated testing. Ensure the quality and reliability of data integration processes through rigorous testing methodologies. Coordinate testing activities across teams, ensuring alignment to delivery plans and environments. Partner with development teams to identify, document, and resolve defects efficiently. Design and implement automation frameworks to streamline testing processes and improve efficiency. Leverage automation tools to enhance the testing lifecycle and reduce manual intervention. Continuously improve automation practices in line with platform and industry capabilities Develop and execute test cases for Data Quality (DQ) rules implemented in Informatica Cloud Data Quality (ICDQ). Validate DQ rule logic, thresholds, transformations, exception handling, and cleansing routines. Perform unit, system, and regression testing for DQ rules across IDMC mappings, mapplets, and integration tasks. Execute end-to-end test cycles covering: Rejection logic Suspense/error queue handling Automated notifications Record cleansing and enrichment routines Ensure consistent DQ rule behaviour across DEV, QA, and PROD environments, validating migration and deployment steps. ExperienceMinimum of 10 years of experience in Testing and documentations, with a focus on Informatica Cloud (IDMC). Proven experience in Testing Specialist with a focus on Informatica Cloud (IDMC) testing and automation Experience operating within regulated environments, including understanding validation, quality, and compliance standards Understanding of the Haleon Quality System and validation requirements, policies, procedures, and standards

ResponsibilitiesTo review of analytical documents generated during the analysis of QC, Stability and Microbiology for adequacy and accuracy. To carry out investigation in-case of out of specification (OOS) and deviation and take the corrective and preventive action (CAPA).To ensure the calibration of all the analysis instruments is accurate.To sign off electronically the final document of sample set generated through Empower and all other software where (E-signature is applicable) for all the analysis in QC, stability & microbiology.To ensure the preparation of working standards as per the guidelines and pharmacopoeias.To review of calculation of the respective test protocol and daily release status.To ensure online recording and documentation of all the data related to the testing on daily basis and ensure the tractability of the same.To check the record of preparation of the reagent and volumetric solutions.To prepare SOP as per the change proposal.

ResponsibilitiesActively Support launch and sustenance of Baxter commercial products globally by following the Baxter Quality Management Systems. Assist in the management of the Baxter product design throughout the product lifecycle and maintenance of the product DHF, or similar product design governance documents for a particular product family. Identify and analyze design problems to achieve optimal solutions that satisfy cost and technical requirements. Formulate new, innovative approaches to solve technical problems on a consistent basis. Actively involve in commercialized product investigation, execute batches in laboratory, prepare report to support the investigation. Involve in compendial product change/proposal discussion, assess the proposed change impact on the product quality & patient safety. Provide support to analytical team by providing the required product solution/placebo solution samples. Execute batches in laboratory, assess the study outcome to support the compendial product change requirement. Ensure response to customer queries, agencies query, market compliance. Design and execute batches/experiments in laboratory, prepare report to support queries/market compliance. Responsible for ensuring the availability of required licenses and materials (raw material, packaging materials) in laboratory.Qualification & ExperienceEducational Qualification: Master’s in Pharmaceutics or equivalent Hands on experience in laboratory batch execution and drive the towards the expected result. Good communication skills for effective liaison and teamwork Problem-solving skills, analytical skills and attention to detail Excellent organizational skills and the ability to work on several tasks or projects concurrently