Qualification & Experience GNM / Bsc Nursing 2 to 4 years of experience   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"

Qualification & Experience MBBS 0-1 years of experience Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Qualification & Experience M.Pharm/Ph.d Experience: 6-8 years   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Responsible for Preparation and Review Analytical method development and validation. To guide team members for cost effective method development. To monitor the execution of R&D samples, stability samples, raw materials and excipients received from contract giver. To provide job training and related advance tories as and when it required. Responsible for execution and approval of Anarytical Instrument Qualification and Calibration. Responsible for preparation, review and approval of STP, SOP, Protocol and its reports. Responsible to ensure all quality related issues are handing as per respective SOP, investigation to identify root. Responsible to maintain and follow GLP and GDP in compliance manner in laboratory. Having the leadership quality and Responsible to build the team. Responsible to develop quality culture     Qualification & Experience M.Sc./M.Pharm, with 10+ years of experience Candidate having more than 10 years of experience Experience in review of HPLC, GC, LCMS and other chromatography systems Preferred-faced regulatory audits like USFDA/MHRA/TGA   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Execution of All IPQA related activities within manufacturing unit. Line clearance, in-process dispensing and sampling activities. BMR/BPR issuance, review and preparation under the guidance of seniors. Issuance of Standard Formats and submitting the documents. Preparation of SOP as per the current organization norms and cGMP guidelines under the observation of seniors. Execute routine IPQA monitoring. Review and approve on-line documentation of manufacturing, testing and packing activity. Investigation of any deviation / abnormal observation. Review the GDP issues in Production / QC / QA and in logbooks. Execute CAPA defined by management/QMS. Review critical quality attributes of products, review trend analysis and keep track of OOT results. Execution of All Process Validation related activities within manufacturing unit. Review process validation, qualification planner. Conduct Material issuance for validations activities. Sample withdrawal during process validation. Record observations in observation sheets for process validation. Coordinate and execute process validation, qualification activities & inform about deviation from planning. New equipment qualification & validation. To help in identification of any deviation and report further. To support in investigation of any product deviation and Out of Specification (OOS). To suggest / recommend the changes in the Standard Operating Procedure (SOP). To help in investigation of OOS and Documentation of the same. To be updated about the new changes in all international and local regulatory requirements. To monitor and implement the Good Manufacturing Practice (GMP) standards in the plant. To help in conducting monthly Corrective and Preventive Action (CAPA) meetings and preparation of CAPA summary report and gather CAPA details generated from individual quality sub-systems (e.g. Deviation, Change Control, OOS, Complaint, External inspection, Self-inspection)   Qualification & Experience B.Sc / M.Sc / B.Pharm / M.Pharm Experience : 02-07+years   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities To carry out the sampling of all the materials according to Standard Operating Procedure (SOP). To carry out the testing of Raw Material and Packing Material according to approved procedure. To release Raw Material and Packing Material. To carry out the calibration of instruments as per the schedule. To prepare the working standards as per the guidelines and various pharmacopoeias. To ensure the status tag on the released material and transfer such material in the released area. To analyze the artworks as per the guidelines. To follow the Good Laboratory practices and Good Manufacturing practices (GMP). To prepare requirement list of chemical & reagent for procurement. To perform the analysis of stability sample as per current specification. To compile the data required for internal quality audit in the plant, as and when required. To implement the cGMP standards.   Qualification & Experience B.Sc / M.Sc / B.Pharm / M.Pharm Experience : 02-07+years   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities To ensure the clean environment for sterile preparation by implementing the Good Manufacturing Practice (GMP) norms as per the international standards and guidelines. To do sampling of Water for Injection (WFI), Double Reverse Osmosis (DRO), Single Reverse Osmosis (SRO), Raw water and pure steam. To analyze water samples for pH, conductivity, Bacterial Endotoxin Test (BET), bioburden, Total Organic Carbon (TOC), pathogens, chlorides, hardness, silt density index and other testing as per the requirements. To analyze the samples of water system after maintenance work . To observe and record the results the microbiological plates and test tubes after analysis as well as supervise discarding method of same. To perform the timely microbiological testing of finished product samples, pre-sterile samples, Raw material as well as Packing material sample as per the requirements and SOPs and record the results for the same.     Qualification & Experience B.Sc / M.Sc / B.Pharm / M.Pharm Experience : 02-07+years   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

 Responsibilities Promote and sell pharmaceutical products to healthcare professionals Establish and maintain strong relationships with existing and potential customers Identify new business opportunities and generate leads Provide product information and educational materials to healthcare professionals Regularly meet sales targets and contribute to the company's growth Attend conferences, trade shows, and other industry events Stay up-to-date with the latest developments in the pharmaceutical industry Collect and analyze market data to identify trends and opportunities     Qualification & Experience Junior candidate with 1 to 3 years of experience in the pharmaceutical sales industry. Excellent communication and interpersonal skills Strong time management and organizational abilities Thorough product knowledge and understanding of the pharmaceutical industry Ability to effectively market and promote products Exceptional customer service skills Knowledge of the healthcare industry and market dynamics  

Qualification & Experience B pharmacy / M pharmacy fresher candidates for Production Department for our Unit-2 plant  0 to 1 year  experience   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Qualification & Experience B.sc (Nursing) / GNM(Nursing) Registration Certificate is compulsory Experience Required :- 0 to 5 Years   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"