Senior Analytical Development Scientist - CMC
Ceredigion
WHO ARE THEY
My client is an industry leading healthcare company looking for a Senior Analytical Development Scientist to join their team on a permanent basis!
THE ROLE
Oversee the development and validation of analytical techniques to support manufacturing activities of new and established biological goods Supervise the characterization of new and established products as part of lifecycle management projects Experienced in developing studies using techniques such as U/HPLC, binding assays (SPR Biacore, BLI, ELISA), SDS and Circular Dichroism Maintain and develop state of the art knowledge applicable to existing and future processes and maintain up-to-date knowledge on regulatory expectations Independently design, plan and manage own studies Represent the CMC team at project team meetings and provide expert technical advice in analytical issues to Quality Control and manufacturing
WHAT YOU WILL NEED
Educated to degree level in an appropriate scientific discipline Significant experience in analytical development in a biopharmaceutical or closely related industry and strong knowledge of regulatory requirements. Computer literate.
BENEFITS
Work for a global organisation Beautiful location Private healthcare Up to 36 days holiday
#J-18808-Ljbffr
Ceredigion
WHO ARE THEY
My client is an industry leading healthcare company looking for a Senior Analytical Development Scientist to join their team on a permanent basis!
THE ROLE
Oversee the development and validation of analytical techniques to support manufacturing activities of new and established biological goods Supervise the characterization of new and established products as part of lifecycle management projects Experienced in developing studies using techniques such as U/HPLC, binding assays (SPR Biacore, BLI, ELISA), SDS and Circular Dichroism Maintain and develop state of the art knowledge applicable to existing and future processes and maintain up-to-date knowledge on regulatory expectations Independently design, plan and manage own studies Represent the CMC team at project team meetings and provide expert technical advice in analytical issues to Quality Control and manufacturing
WHAT YOU WILL NEED
Educated to degree level in an appropriate scientific discipline Significant experience in analytical development in a biopharmaceutical or closely related industry and strong knowledge of regulatory requirements. Computer literate.
BENEFITS
Work for a global organisation Beautiful location Private healthcare Up to 36 days holiday
#J-18808-Ljbffr
