Responsibilities: To assist and advise others on work, including validation and research projects Multiple scientific project management
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- efficiently running 2 key projects within Chemistry and/or Biochemistry/Immunology related subject areas.
To maintain current legislation, regulatory requirements, interpret and develop additional systems/available data where specified To interpret experimental results and collate data for use in regulatory submissions, notifications and peer reviewed publications To provide product support to customers within the Company, especially Regulatory Affairs, QA, QC and Sales in the development and validation of products and processes to meet business needs and current legislation To maintain project lead times and run key projects ensuring the interpretation of business requirements for product development.
To also ensure that project details are communicated to all sponsors and stakeholders and communicate project requirements to the Method Development Manager and /or Global Head of Development Author high quality scientific technical reports, papers and presentations Lead and assist in research and development of complex techniques Requirements: Relevant PhD 3 years industry experience Member of a learned society (RSC, RSB, RPS) Proven ability to develop and validate analytical methods High level of scientific understanding Experience of developing analytical methods in Pharma Knowledge of method validation Good statistical and data interpretation knowledge