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  • Handling of production equipment. * Documentation capabilities like filling of BMR / BPR etc. * Knowledge of basic cGMP *Food & Drug Administration Maharashtra State Liquid & Oral S Certificate is Mandatory

  • Handling of production equipment. * Documentation capabilities like filling of BMR / BPR etc. * Knowledge of basic cGMP *Food & Drug Administration Maharashtra State Liquid & Oral S Certificate is Mandatory

  • Maintaining relationship with existing as well as new Doctors Assess clients needs and present suitable promoted products Provide product information and deliver product samples Monitor and analyze data and market conditions to identify competitive advantage Pursue continuous learning and professional development and stay up-to-date with latest medical data

  • SSZ INFOTECH 22 years old organization Medical Transcription JOBS for Freshers / Housewives / Teachers / Retired Professionals / BAMS / BHMS We are recruiting any Graduates with good English communication skills MT’s start their career with a pay scale of Rs. 10,000/- to 15,000 per month. With little Experience, MT’s can earn Rs.30,000/- per month and are eligible for other perquisites and benefits. Medical ...

  • SSZ INFOTECH is a 22-years old organization in Health care sector. URGENT and IMMEDIATE Requirement at SECUNDERABAD Female Graduates Fresher’s or experienced, with good Communication skills Undergraduates with experience and EXCELLENT ENGLISH communication abilities can also apply This is a permanent position for the right candidate Eligibility: B Tech / BCom / BA/ BSc Female Graduates Fresher’s or ...

  •  Building rapports and talking to manufacturer in India.  Negotiation for rates.  No targets to be achieved  Fresher Sourcing Executive The candidate must have good communication skills He must be a graduate He must have basic computer knowledge Fresher candidates ...

  • Reports: Pricing & Reimbursement reports, this includes data pulling, standardization & calculations. • Portal: Updating, pricing & reimbursement information on tool & maintaining it. • Analytics: Performing various task of analysis using our database. Pricing analysis • Calculations: COT (cost of treatment) calculation with help of extensive research. • Research: Conducting market research on pharmaceutical products and ...

  • Reports: Pricing & Reimbursement reports, this includes data pulling, standardization & calculations. • Portal: Updating, pricing & reimbursement information on tool & maintaining it. • Analytics: Performing various task of analysis using our database. Pricing analysis • Calculations: COT (cost of treatment) calculation with help of extensive research. • Research: Conducting market research on pharmaceutical products and ...

  • Reports: Pricing & Reimbursement reports, this includes data pulling, standardization & calculations. • Portal: Updating, pricing & reimbursement information on tool & maintaining it. • Analytics: Performing various task of analysis using our database. Pricing analysis • Calculations: COT (cost of treatment) calculation with help of extensive research. • Research: Conducting market research on pharmaceutical products and ...

  • Reports: Pricing & Reimbursement reports, this includes data pulling, standardization & calculations. • Portal: Updating, pricing & reimbursement information on tool & maintaining it. • Analytics: Performing various task of analysis using our database. Pricing analysis • Calculations: COT (cost of treatment) calculation with help of extensive research. • Research: Conducting market research on pharmaceutical products and ...

  • Reports: Pricing & Reimbursement reports, this includes data pulling, standardization & calculations. • Portal: Updating, pricing & reimbursement information on tool & maintaining it. • Analytics: Performing various task of analysis using our database. Pricing analysis • Calculations: COT (cost of treatment) calculation with help of extensive research. • Research: Conducting market research on pharmaceutical products and ...

  • Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Determine regulatory reportability of cases obtained from clinical trials, spontaneous and solicited reports within assigned therapeutic team and across all products/sites, as necessary, and in a timely fashion Determine seriousness and relatedness across products as ...

  • Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Determine regulatory reportability of cases obtained from clinical trials, spontaneous and solicited reports within assigned therapeutic team and across all products/sites, as necessary, and in a timely fashion Determine seriousness and relatedness across products as ...

  • Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Determine regulatory reportability of cases obtained from clinical trials, spontaneous and solicited reports within assigned therapeutic team and across all products/sites, as necessary, and in a timely fashion Determine seriousness and relatedness across products as ...

  • Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Determine regulatory reportability of cases obtained from clinical trials, spontaneous and solicited reports within assigned therapeutic team and across all products/sites, as necessary, and in a timely fashion Determine seriousness and relatedness across products as ...

  • Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Determine regulatory reportability of cases obtained from clinical trials, spontaneous and solicited reports within assigned therapeutic team and across all products/sites, as necessary, and in a timely fashion Determine seriousness and relatedness across products as ...

  • Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Determine regulatory reportability of cases obtained from clinical trials, spontaneous and solicited reports within assigned therapeutic team and across all products/sites, as necessary, and in a timely fashion Determine seriousness and relatedness across products as ...

  • Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Determine regulatory reportability of cases obtained from clinical trials, spontaneous and solicited reports within assigned therapeutic team and across all products/sites, as necessary, and in a timely fashion Determine seriousness and relatedness across products as ...

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