ResponsibilitiesCompetencies Collaboration Customer Centricity Developing Talent Innovation & Creativity Process Excellence Result Orientation Stakeholder Management Strategic Agility

ResponsibilitiesValidation & Qualification Management Preparation, review, and approval of: User Requirement Specifications (URS) Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) Computer system validation (CSV) Quality Control laboratory equipment qualification SOP and Protocols preparation; review and approval Execution of FAT/SAT and commissioning supportExpeirenceBachelor / Master of Pharmacy / Master of Science 07 to 09 years

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.

 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

ResponsibilitiesManage and oversee packaging operations to ensure pharmaceutical products are packaged in accordance with established specifications and quality standards Oversee the operation and optimization of packaging equipment including automated packaging systems, blister packing machines, bottle filling and capping equipment, and cartoning and labeling systems Manage packaging personnel including scheduling, training, and performance management to ensure adequate work coverage Ensure accurate and complete batch documentation and packaging records are maintained as required by regulatory standards Contribute to maintaining a clean, organized, and compliant work area in accordance with area cleaning and sanitization protocols Identify, document, and report deviations and non-conformances during packaging activities in accordance with established quality procedures Lead continuous improvement efforts in packaging operations by identifying and implementing process improvements Ensure compliance with cGMP, regulatory requirements, and internal quality standards across all packaging activities Qualification & ExpeirenceB. Pharm B. Pharm - Required M. Pharm M. Pharm - Preferred Experience: 8 years or more in 8 - 10 Years

ResponsibilitiesTo follow the safety rules in the premises according to the company norms. Monitoring of DP, RH and temperature area in their visual inspection Responsible for Operation and Cleaning of Wrap around labeling machine, Autocartonator machine, Online check weigher, track and trace system, Bopp taping machine with weighing balance and PFS machines. Responsible for labeling and packing of products as per BPR. Responsible to perform visual inspection of the products /media filled vials or PFS as per the sop. Responsible for Operation and cleaning of Automatic visual inspection machine and X-RAY inspection machine. Operation and cleaning of visual inspection table and Operation of Lux meter. Responsible to perform the in process checks during operation.Qualification & Experience4 years or more in 2-3 yearsBachelor Degree (BS) - B. Sc./ B.Pharma. - Required Master Degree (MS) M. Sc. - Preferred

ResponsbilitiesMaintain and effectively communicate deep scientific knowledge: Engage in continuous learning to maintain the highest level of technical expertise within oncology. This will enable the MSL to answer deep scientific questions and be sought after by their customers based on peer-credible knowledge and expertise. As a result, the MSL will establish themselves as a reliable, trusted resource of unbiased, accurate, up-to-date medical and scientific knowledge. Excel at customer engagement and support medical/scientific information needs of scientific experts: Through the application of emotional intelligence and a deep understanding of their customers, the MSL will act as one of the primary interfaces between Lilly medical and scientific experts to deliver the best-in-class customer experiences. Core to the role is to answer customer questions by providing deep and advanced disease state and product information. Additionally, the MSL will connect scientific experts with other Lilly resources or internal business partners as appropriate and identify possible collaborative research or external collaborations. Strategic vision and leadership: Synthesize complex data and effectively communicate meaningful clinical insights and unanswered customer questions they receive from scientific experts to Lilly medical and cross-functional teams. The MSL will use creative problem-solving skills and utilize internal resources effectively to execute upon solutions. The MSL will use a principle-based approach to make decisions independently or escalate them appropriately. They cultivate internal networks and collaborate effectively across functions with an active contribution to medical planning and strategy in Lilly India. Territory ownership: The MSL will be expected to demonstrate strategic analysis, planning, and prioritization to maximize efficiency. They will implement and evaluate a strategic territory plan prioritizing core MSL activities and take personal accountability for results. The MSL will execute the role in a compliant manner, adhering to all governing internal and external requirements, procedures, and laws, demonstrating good judgment at all times.

ResponsibilitiesA professional approach must be adapted with all patients, staff and visitors. To provide medical cover, routine and emergency, during hours of duty and work in conjunction with the other specialties to serve the institute. Follow all Clinical safety, hygiene, infection control protocols to be adhered to (e.g. wearing gloves when required, aprons, hand hygiene, etc) Is required to be willing and available to see patients when required or when requested. Required to actively participate and contribute in Classroom and bedside teaching programs for postgraduate students. Required to assist the consultants in the operation theatre and can assist in surgeries under supervision of consultants. Required to be skilled and knowledgeable enough to identify the complex surgical problems take appropriate action in case of emergency with permission by treating consultant. Required to supervise post graduate students; however, the attending surgeon is ultimately responsible for the care of the patient. Supervise the daily clinical management of all patients in conjunction with the RMOs and under the guidance of Consultants Ensure that patient report and documentation is complete and consents for surgery and procedures are taken. Effective communication with patients, family, colleagues and other health care workers. Treatment sheets are to be written with diagnosis in capital letters, whenever situation demands it. Each treatment sheet should be dated, named and signed by the writing doctor. Doctors should refer to the progress notes while writing treatment sheets. Required to accompany respective Consultants for rounds apart from taking independent rounds themselves and should follow up the patients for any further care (change in plan of Treatment).Qualification & Experience0 - 5 YearsQualificationMBBS, and MD/DNB/MS (Specialization as per the dept’s requirement of qualification)

Responsibilities  Coordinating smooth stay of the patients from admission till discharge  Attending clinical meetings/ CME Programs  Ensures compliance of Hospital policies and proceduresQualification & Experience Degree in MBBS , BAMS/BHMS  Degree in medical science Fresher Or Experienced Are Preferred.