Responsibilities Sampling and analysis of Raw materials, Packing materials, In process, Intermediate and Finished products Calibration of Quality Control instruments Conducting Stability/Holding time studies Handling of Reference Standards and qualification of Working Standards Analyst qualifications Analytical Method Validation. Management of Control samples (Retain sample) Conducting OOS investigations (Phase-1)   Qualification & Experience 2-3 years experience in Pharmaceutical Quality Control M.Pharmacy/B.Pharmacy/M.Sc. (Chemistry)/B.Sc. (Chemistry) Experience in handling HPLC, GC and other Quality Control instruments preferred Good documentation skills with exposure to GLP, GDP and cGMP practices  

Responsibilities Business development and marketing of APIs to Generic Pharmaceutical Companies in domestic, emerging markets and EU markets for a few products. Finding and selecting new Customers, distributors, and agents in the concerned market. Playing a significant role in planning the strategic road map of the organization by setting up a product selection process in the company and, designing the product pipeline and prioritization for planned future.   Qualification & Experience 5-7 years for Assistant Manager and 8-10 Years for Manager. Experience of sales, business development or corporate strategy in Pharma industry is required B.Pharmacy/ M.Pharmacy/ MBA  

Qualification & Experience  ITI / D.Pharma / B.Pharma. (with relevant experience) 02-08 Years (Granulation, Compression, Coating, Primary & Secondary Packing).   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Qualification & Experience M.Pharm / B.Pharm / M.sc 2 to 6 years of experience   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Development and implementation of Standard Operating Procedures (SOPs). Review and perform signal management activity as per guideline and SOP. Preparation, review & reporting of aggregate reports (Such as PADER, PBRER & PSUR) as per regulatory requirement with compliance to guideline & SOP. Oversight of in-house & out-sourced PV activities & maintain monthly compliance process. Ensure compliance (quality, procedures, regulations, timeliness, consistency) of aggregate reports, Signal management & all EU activities. Facilitate safety monitoring by optimising scientific quality documentation & data entry of safety case reports including spontaneous litigation reports. Management of ICSR activities as per respective regulatory requirements including safety data accuracy in safety databases. Responsible for partner/vendor audit and communication for all PV activity. Preparation and review of SDEA. Handling of RMP program in line with innovator for UK & EMA. Management of XEVMPD & SPOR databases with timely update safety variation in line with Art. 57 guideline.   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Qualification & Experience M.sc  Plus 12 years of experience   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Qualification & Experience GNM & BSC 1+ Years of Hospital Relevant Experience Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Qualification & Experience B.Pharm/Diploma in Pharmacy/M.Pharm 2+ Years of Hospital Relevant Experience   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Qualification & Experience Any Graduate 1+ Years of Hospital Relevant Experience   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities You will be responsible for adhering to GLP (Good Laboratory Practices) and safety practices, and ensuring compliance with the SOP (Standard Operating Procedure). Your responsibilities include analysis of samples as assigned by the group leader, ensuring adherence to relevant SOPs and Standard Testing Protocols (STPs), and following online documentation and calculation practices. You will also be responsible for authorized transactions in SAP and LIMS (Laboratory Information Management System), as well as the online reporting of any Out-of-Specification (OOS), Out-of-Trend (OOT), and incidents to the group leader. You will be responsible for verifying that analytical results are conforming with specification limits. You will maintain and monitor 5S practices in the laboratory, perform sample management for the team and handle any other responsibilities assigned by the team leader.     Qualification & Experience 5 to 8 years of experience in a laboratory setting, preferably in pharmaceutical or related industries