ResponsibilitiesPrevent incidences across Unit to ensure employees and stakeholder¢�s safety Assess and Improve emergency preparedness across Unit to reduce impact of Incidences to human and propertyExecution of the planned Activity, promotional Activity and improvement and Statutory complianceQualification & ExperienceScience graduate in chemistry/ Diploma or Degree with Diploma in Advance industrial safety Relevant Work Experience 2 years of safety experience in Pharma or chemical industries

ResponsibilitiesPerform method transfers/ validations / method verifications to the complex analytical techniques Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions. Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies. Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current. Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database. Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction. Qualification & ExpeirneceMaster’s degree in chemistry/ pharmacy with 8-10 years of experience in Analytical Method Transfer / Validation) Qualified in multiple analytical techniques (HPLC-with Empower, GC, IC, ICP-MS, Potentiometry, UV?Vis, FTIR, Karl Fischer, and pH meters) Demonstrated technical skills in method validation and testing Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Conduct analytical method validation in accordance with ICH Q2 (R1/R2), USP, and EP standards, encompassing protocol preparation, execution, approval of validation summaries, and coordination with cross?functional teams. Conduct test method GAP assessments against USP, EP, BP, and JP requirements for New Product Introduction (NPI). 

ResponsibilitiesTo perform QC activities in order to ensure quality of products and services and maintain related documentation to adhere to quality operations and regulatory requirements. Qualification & ExperiencePOST GRADUATE IN CHEMISTRY/PHARMACY Experience: 3-5 years in a Quality Control/Analysis laboratory in a cGMP/ISO environment, with exposure to method development and validation activities

ResponsibilitiesImplementing monthly production schedule with consistent quality, adhering to Regulatory, GQS, and HSE guidelines, with proper utilization of resources and optimum cycle time. Performing the production activities in assigned areas in order to achieve 100 % customer service. Performing the SAP related activities Able to handle the team consist of Contractual persons ,FTC & Operators in allocated shift Able to do troubleshooting in the allocated areaQualification & ExperienceB.Pharm (Bachelor of Pharmacy) , M.Pharm (Master of Pharmacy) Experience 1 to 6 years in pharmaceutical manufacturing (Preferably in Packing )

ResponsibilitiesIP Landscape Preparation, FTO searches & preparing evaluation reportsIP litigation support: Provide litigation support including review of documents, discovery and coordinate with various internal stakeholders and counsel.Pre-PIF assessments: Preparation of prosecution summary of relevant patents, IP Summary etc.Timely support to Portfolio, Business Development, R & D, PMO, and Regulatory teamsNew Product Opportunity Identification - based on IP scenariosMonitoring of IP updates, Competitive Intelligence and regulatory developmentsQualification & Experience Master of Pharmacy or M.S. (Pharma) or M. Tech. (Pharma) or Ph.D. (Pharma) (Pharmaceutics or Chemistry preferred) from reputed institute.At least 8-10 years of relevant experience in IP domain

ResponsibilitiesReceipt, evaluation and logging of complaints into TrackWise.Receipt, evaluation and logging of customer queries.Coordinate with internal & external stakeholders involved in the complaint handling process.Provide the acknowledgement and the response letter to the complainant.Reconciliation of received Product Quality Complaints.Qualification & Experience B.Pharma / M.Sc (Life Sciences)5-6 Years

ResponsibilitiesTo dispense prescriptions accurately and promptly.To actively participate in the creation of the Pharmacy FormularyTo process Billing of dispensed items for inpatient and outpatients.To implement the SOP’s.To provide drug information to patients and other healthcare Professionals.To ensure proper storage and record keeping of drugs.To maintain up to date knowledge about all drugs and medical supplies.To review and monitor patient profiles of orders, cost effectiveness of drugs and intervenes appropriately.To play an active role in ensuring proper inventory control systems including, control and monitoring of stocks, introduction of new items, removal of non moving and expired stock.To be well groomed, punctual & adhere to company policies and practices.To have complete orientation of QMS and EMS system of Hospital.To have complete Awareness about Disaster Management Programme (DMP) of the hospital.To Comply with the service quality Process, environmental & occupational issues & policies of the respective area.To comply with patient safety policy.To ensure safe utilization of equipments and proper waste disposal systemQualification & Experience B Pharma D Pharma

ResponsibilitiesOversee pharmacy operations and maintain the required stock of medicinesDispense medications as prescribed by the Medical OfficerVisit and educate the community on healthBuild the capacity of community health workersQualification & Experience A diploma or bachelor’s degree in pharmacy with 5 years of relevant work experienceAn active registration with the Karnataka State Pharmacy Council (KSPC)Familiarity with MS Office tools, POS software and ERP / related softwareAn unwavering commitment to serve the communities, and the resilience to work full-time (6 days a week, Mon-Sat) in an evolving environmentFluency in Kannada and Hindi language is preferred

ResponsibilitiesTo supervise compliance to all cGMP, GxP, or any other regulatory requirements, including EH&S requirements. Complete self-training and monitor training of team members on the relevant SOPs. Authorization of standard operation procedures and ensure its implementation. Handling of product recalls. Approval of annual product report. Report any quality concerns or suggestions for improvements to HOD. Execute and supervise all tasks and activities as per the applicable SOPs. Responsible to complete the assigned trainings, applicable for workgroup “Manufacturing-Manager-Goa” in the L2LMS. Overall responsibility to ensure effective and efficient manufacturing/packing operation to meet the sales and distribution requirements. To ensure that the Products are produced and stored in accordance to appropriate documentation to obtain required quality. To ensure preparation of all documents as & when required of production department and to approve instructions/documents related to production and ensure their strict implementation.Qualification & Experience10 - 15 years experience in manufacturing. Education Graduation in Pharmacy

Qualification & Experience           Deptt : Pharmacy     Qualification : Dip. Pharm/B.Pharm                  Experience : 1+ years