Scientist II, Bioanalytical

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Irfa******

  • India 
  • Last Update: 30.05.2019 at 12:00

Job Type
Full Time
Start
May , 2019
Duration
6 Month
Place
Hyderabad
Country
India

Category


Regulatory, Quality and Clinical

Description


Responsibilities:Complying with editorial policies and conventions.Achieve production volume and quality targets.Recording performance against target.Taking an active role within the team to ensure targets are met.Maintain awareness of current developments in own technology areas.Achieve and maintain consistent quality standards.Effective personal planning and time management.Maintain a flexible and adaptable approach towards process change.To take responsibility for identifying technology training and developmental needs for yourself on an on-going basis.To make positive efforts to promote personal safety and that of others by taking reasonable care at work, by carrying out the requirements of the law or following recognised codes of practice provided or advised by management to ensure safe working practices.To undertake any other reasonable duties as requested by your line manager / director on a permanent or temporary basis.Topics to be prepared:Patent basics, basic biotechnological concepts, biological drugs, eg antibodies, protiens, RNA interference agents; gene therapy, biomarkers, vaccines, cell culture methods, protein purification and isolation techniques, drug delivery methods and devices, diagnostic techniques, brief knowledge on pharma companies, basics in molecular genetics (eg gene modifications using CRISPR), good comprehensive writing skills

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