Messina Group is looking for a remote Senior Consultant of Analytical Services to work with our client out of their home office with 50% travel. 

Essential functions

  • Manages multiple analytical projects related to the development, qualification and/or troubleshooting of sensitive, efficient, and reliable assays for a wide class of biological molecules simultaneously.
  • Prepares, reviews, and edits method transfer, qualification, and validation protocols, analytical technical reports, and CMC regulatory documentation. 
  • Writes regulatory documentation.
  • Provides technical expertise and advises project representatives/teams on topics pertaining to biopharmaceutical analysis and CMC development, including assay development and selection, structure-activity relationships, product characterization strategy, impurity identification, Quality-by-Design, product quality attribute classification, and study design. Often presents findings and/or results to client senior management.
  • Communicates effectively in a timely manner with external and internal clients regarding technical, scientific, and other project-related issues and progress.
  • Provides technical guidance to others in resolving challenging issues relating to analytical methods
  • Supports our clients marketing efforts by actively seeking new clients and repeat business opportunities.
  • Keeps current with technical developments in the industry and regulatory agency thinking.
  • Types of Projects: Recombinant proteins, peptides, oligonucleotides, Gene and Cell Therapies
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Senior Consultant, Analytical Services | Direct Hire

Remote, IL

Messina Group is looking for a remote Senior Consultant of Analytical Services to work with our client out of their home office with 50% travel. 

Essential functions

  • Manages multiple analytical projects related to the development, qualification and/or troubleshooting of sensitive, efficient, and reliable assays for a wide class of biological molecules simultaneously.
  • Prepares, reviews, and edits method transfer, qualification, and validation protocols, analytical technical reports, and CMC regulatory documentation. 
  • Writes regulatory documentation.
  • Provides technical expertise and advises project representatives/teams on topics pertaining to biopharmaceutical analysis and CMC development, including assay development and selection, structure-activity relationships, product characterization strategy, impurity identification, Quality-by-Design, product quality attribute classification, and study design. Often presents findings and/or results to client senior management.
  • Communicates effectively in a timely manner with external and internal clients regarding technical, scientific, and other project-related issues and progress.
  • Provides technical guidance to others in resolving challenging issues relating to analytical methods
  • Supports our clients marketing efforts by actively seeking new clients and repeat business opportunities.
  • Keeps current with technical developments in the industry and regulatory agency thinking.
  • Types of Projects: Recombinant proteins, peptides, oligonucleotides, Gene and Cell Therapies

Learn More:

John Dewar

Sr. Talent Advisor

jdewar@messinagroupinc.com

(847) 692-0624

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