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)
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