- job summary: Ready to leverage your expertise in medical review to shape promotional materials and drive strategic initiatives? We're seeking a Medical Reviewer/Safety Reviewer III to join our team on a contract basis. In this hybrid role based in Florham Park, NJ, you'll be instrumental in ensuring the accuracy and compliance of branded and unbranded content by providing crucial medical input throughout the Medical, Legal, and Regulatory (MLR) review projob summary: Ready to leverage your expertise in medical review to shape promotional materials and drive strategic initiatives? We're seeking a Medical Reviewer/Safety Reviewer III to join our team on a contract basis. In this hybrid role based in Florham Park, NJ, you'll be instrumental in ensuring the accuracy and compliance of branded and unbranded content by providing crucial medical input throughout the Medical, Legal, and Regulatory (MLR) review pro
- job summary: Primary responsibility is large scale recombinant protein production operations for commercial production through execution of SOPs, Batch Records, and all associated cGMP activities in the manufacturing facility. Duties include operation, maintenance, cleaning (CIP) and sterilization (SIP) of large scale cell culture bioreactors and associated operations such as media preparation, infection and harvest. The incumbent is capable of identifyinjob summary: Primary responsibility is large scale recombinant protein production operations for commercial production through execution of SOPs, Batch Records, and all associated cGMP activities in the manufacturing facility. Duties include operation, maintenance, cleaning (CIP) and sterilization (SIP) of large scale cell culture bioreactors and associated operations such as media preparation, infection and harvest. The incumbent is capable of identifyin
- job summary: Step into a vital role supporting the production of a key vaccine product at a well-established pharmaceutical manufacturing site in Pearl River, NY. This 100% onsite opportunity is perfect for candidates with 1-2 years of cGMP manufacturing experience and familiarity with systems like SAP, Veeva, and LIMS. You'll be part of the team responsible for producing drug substance through downstream processing techniques such as filtration, centrifujob summary: Step into a vital role supporting the production of a key vaccine product at a well-established pharmaceutical manufacturing site in Pearl River, NY. This 100% onsite opportunity is perfect for candidates with 1-2 years of cGMP manufacturing experience and familiarity with systems like SAP, Veeva, and LIMS. You'll be part of the team responsible for producing drug substance through downstream processing techniques such as filtration, centrifu
