Roles and Responsibilities Arranging appointments with doctors and pharmacists, which may include pre-arranged appointments or regular calling. Meet the number of Doctor and Chemist calls per day as decided by respective divisions as per company policy. Making presentations (detailing) to doctors, specialists, etc. Do chemist survey to ensure availability of products. Facilitating Medical conferences. Ensure proper distribution of samples and promotional scientific materials to selected Doctors. Building and maintaining positive working relationships with chemist and stockiest Planning work schedules and weekly and monthly tour programme. This may involve working with your superiors and HO staff. Regularly attending company meetings, product launch and briefings. Ensure on time payment collection and sales and stock data from stockiest. Monitoring competitor activity and competitors' products; Developing strategies for increasing opportunities and have discussion with Medical Services to resolve Drs queries. Staying informed about new hospital, or doctor in territory. Desired Candidate Profile - Age Upto 21-28 years. - Bpharma/BSC Freshers can also apply salary 3.75 Lacs - Any graduates with minimum 1 year experience in pharma selling can apply.
Position: Asst. Manager Qualification: M.Pharm /B.Pharm/M.Sc. having 8+ years experience in EU/ LATAM market Job profile: 1. Responsible for the designated regulatory projects with respective deadlines 2. Expertise in authoring CMC documentation for EU MAA and post-approval submissions with hands-on experience on using eCTD software Good coordination skills with stakeholders on regular basis to source the documents in accordance with project timelines Review the documents against the Agency guidances assuring regulatory compliance Keep knowledge up to date about regulatory guidelines 6. Manage administration of regulatory documentation and ensure the traceability of regulatory history (filing, archiving, database etc) Position: Sr.Officer/ Executive Qualification : M.Pharm /B.Pharm/M.Sc. having 4-6 years experience in US market Job profile: 1) Author and compile CMC documentation for ANDA filings and post-approval submissions 2) Coordination with stakeholders on regular basis to source the documents in accordance with project timelines 3) Review the documents against the FDA guidances assuring regulatory compliance 4) Keep knowledge up to date with regard to regulatory guidelines 5) Hands-on experience on using eCTD software Position: Officer Qualification : M.Pharm /B.Pharm/M.Sc. having 2-3 years experience in US market Job profile: 1) Author and compile CMC documentation for ANDA filings and post-approval submissions 2) Coordination with stakeholders on regular basis to source the documents in accordance with project timelines 3) Review the documents against the FDA guidances assuring regulatory compliance 4) Keep knowledge up to date with regard to regulatory guidelines 5) Hands-on experience on using eCTD software Position: Asst. Manager/ Sr.Exexcutive Qualification : M.Pharm /B.Pharm/M.Sc. having 8+ years experience in US market Job profile: 1) Responsible for the designated regulatory projects with respective deadlines 2) Expertise in authoring CMC documentation for ANDA filings and all post-approval submissions 3) Good coordination skills with stakeholders on regular basis to source the documents in accordance with project timelines 4) Review the documents against the FDA guidances assuring regulatory compliance 5) Keep knowledge up to date with regard to regulatory guidelines 6) Manage administration of regulatory documentation and ensure the traceability of regulatory history (filing, archiving, database etc)
Finalization of accounts, Cash flow (in-flow) projections, Supervision of billing, collections, banking, statutory compliances Periodical MIS & Budgeting Correspondence to bankers on financing & Debt Management Role & responsibilities CHARTERED ACCOUNTANT PREFERABLE
Role & responsibilities Time Office Management Recruitment Onboarding activities Offer letter, Appointment letter, confirmation letter drafting and issuance Documents filing work Contract labour Management Exit Formalities Mediclaim activities PMS Training and development Employee Engagement Compliance according to the law. Preferred candidate profile Immediate joiner proffered
Role & responsibilities Responsible for purchase of Lab and R&D Chemicals. Engineering, Instruments, AMC / CMC. Identify new vendors for KSM, Solvent, Raw materials and packaging material. Coordinate with vendor for material procurement as well as timely delivery of material. Maintain approved supplies and vendor list. Calculate vendor Q Score on annual basis. Responsible to prepare MOP data of purchase department for ISO/ EHS. Responsible for preparation, changes and release Purchase order for Raw material, Packing material, Import material, Lab chemicals. Responsible for preparation of Purchase related SOPs & related documents. Responsible for reviewing and maintaining of all the Quality Management System (QMS) documents and SOPs. Initiate & Implement action plan to achieve department objectives. Responsible for vendor development, monitoring of vendor performance. Handle electronic system like SAP, eDMS, eQMS, and LMS. Preferred candidate profile
Role & responsibilities Literature search and review from all the available sources related to product. Targeting the development of stable, scalable, bio-equivalent and Cost- effective generic formulations To discuss with the higher designees such as team leader regarding the development strategy and plan. Ensure product formulations comply with product label claims and established specification. Finding Ways to enhance solubility of newly found drugs Preparing Thermo cycling study protocol, thermal excursion study protocol and photostability protocol for prepared batches. Ensure Product formulations are as per FDA guidance and regulations. Conducted bench trials, Pilot trials and stability studies for new product development and reformulation. Formulation Development involving in various steps like Literature Search, Reference Product Characterization. Check Updates, latest information, guidance form Daily Med and Drugs @FDA,Dissolution Database, IIG limits, Monographs, New Approvals and Submissions etc. Indenting Raw Materials, API, Reference Products, tooling and Coating Materials etc. Co-ordination with various departments like Analytical, Regulatory Affairs, QA, Technology Transfer, Production. To maintain lab and instruments/equipment usage records. Maintained accurate LNB records of all experimental data. Preparation of various document such as stability protocol, MFC, Stability Compilation data, PDR, Tech Transfer documents. Preferred candidate profile
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