High End Jobs in Petaluma, CA

Job ProfileWe are seeking a Quoting Executive to manage and complete inquiries from various channels product sectors and end-markets. This role plays a key part in ensuring the highest level of customer service by providing accurate and timely quotations supporting controlled substance inquiries and...

Job DescriptionThe Oligo Manufacturing Technician I is responsible for supporting Molecular Biology Conversion manufacturing in an ISO 9001 (Custom RUO) and/or ISO 13485 (DxGMP) regulated environment. This position performs production procedures in compliance with current Good Manufacturing Practice...

Position SummaryThe Oligo Manufacturing Technician I is responsible for supporting Molecular Biology Conversion manufacturing in an ISO 9001 (Custom RUO) and/or ISO 13485 (DxGMP) regulated environment. This position performs production procedures in compliance with current Good Manufacturing Practic...

Position SummaryThe Oligo Manufacturing Technician I is responsible for supporting Molecular Biology Conversion manufacturing in an ISO 9001 (Custom RUO) and/or ISO 13485 (DxGMP) regulated environment. This position performs production procedures in compliance with current Good Manufacturing Practic...

This is an Swing Shift: Monday-Thursday (4 x 10 hours 1pm - 11:30pm).The QC Associate Scientist brings scientific experience to LGC and is open to both learning more and sharing knowledge with others. You will be part of an ambitious and collaborative team that strives for flawless execution in all...

Position Summary: This role is responsible for the manufacturing of Controlled Pored Glass (CPG) materials by following established and robust protocols. This position will primarily work with solid phase chemistry that is used in oligo manufacturing.CPG material manufacturing includes amine and nuc...

Explore an outstanding opportunity to join a world-class team at LGC as a Scientist I this role you will play a crucial part in supporting therapeutic oligonucleotide manufacturing by flawlessly transferring processes from development stages to GMP manufacturing. You will author essential documenta...