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Research Associate/Sr. Research Associate - Upstream
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Job Description
My client is a dedicated contract development and manufacturing organization ( CDMO
) focused on development and cGMP manufacturing of biopharmaceutical products derived from mammalian cell culture. They provide a comprehensive range of process development, high qu
Dec 05,2018
USA-CA-Tustin
Research Associate/Sr. Research Associate - Upstream
) focused on development and cGMP manufacturing of biopharmaceutical products derived from mammalian cell culture. They provide a comprehensive range of process development, high quality cGMP clinical and commercial manufacturing services for the biotechnology and biopharmaceutical industries. The
Dec 05,2018
USA-CA-Tustin
Research Associate/Sr. Research Associate - Upstream
Job Type
Direct Hire
Date
Dec 05, 2018
Job ID
2644097
My client is a dedicated contract development and manufacturing organization ( CDMO
) focused on development and cGMP manufacturing of biopharmaceutical products derived from mammalian cell culture. They provide a comprehensive range of process
Dec 05,2018
USA-CA-Tustin
Research Associate/Sr. Research Associate - Upstream
My client is a dedicated contract development and manufacturing organization ( CDMO
) focused on development and cGMP manufacturing of biopharmaceutical products derived from mammalian cell culture. They provide a comprehensive range of process development, high quality cGMP clinical and commercia
Dec 05,2018
USA-CA-Tustin
Research Associate/Sr. Research Associate - Upstream
Job Type:
Direct Hire
Salary:
$65,000.00 - $75,000.00
Date:
12/5/2018
Job ID:
02644097
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Job Description
My client is a dedicated contract development and manufacturing organization ( CDMO
) focused on development and cGMP manufacturing of bi
Dec 05,2018
USA-CA-Tustin
Research Associate/Sr. Research Associate - Upstream
My client is a dedicated contract development and manufacturing organization ( CDMO
) focused on development and cGMP manufacturing of biopharmaceutical products derived from mammalian cell culture. They provide a comprehensive range of process development, high quality cGMP clinical and commercial
Dec 05,2018
USA-CA-Tustin
Research Associate/Sr. Research Associate - Upstream
My client is a dedicated contract development and manufacturing organization ( CDMO
) focused on development and cGMP manufacturing of biopharmaceutical products derived from mammalian cell culture. They provide a comprehensive range of process development, high quality cGMP clinical and commercial
Dec 05,2018
USA-CA-Tustin
Research Associate/Sr. Research Associate - Upstream
Job Description
My client is a dedicated contract development and manufacturing organization ( CDMO
) focused on development and cGMP manufacturing of biopharmaceutical products derived from mammalian cell culture. They provide a comprehensive range of process development, high quality cGMP clinica
Dec 05,2018
USA-CA-
Research Associate/Sr. Research Associate - Upstream
My client is a dedicated contract development and manufacturing organization ( CDMO
) focused on development and cGMP manufacturing of biopharmaceutical products derived from mammalian cell culture. They provide a comprehensive range of process development, high quality cGMP clinical and commercial
Dec 05,2018
USA-CA-Tustin
Research Associate/Sr. Research Associate - Upstream
Job Type
Direct Hire
Date
Dec 05, 2018
Job ID
2644097
My client is a dedicated contract development and manufacturing organization ( CDMO
) focused on development and cGMP manufacturing of biopharmaceutical products derived from mammalian cell culture. They provide a comprehensive range of process
Dec 05,2018
USA-CA-Tustin
Research Associate/Sr. Research Associate - Upstream
My client is a dedicated contract development and manufacturing organization ( CDMO
) focused on development and cGMP manufacturing of biopharmaceutical products derived from mammalian cell culture. They provide a comprehensive range of process development, high quality cGMP clinical and commercia
Dec 05,2018
USA-CA-Thousand Oaks
Technical Writer - Quality or document control, Medical Device or regu
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Job Description:
Looking for a Document Management Specialist for development of regulated or process documents with the ability to deliver high quality documentation including technical writing. The primary responsibilities may include, but are not limited to the following:
Dec 06,2018
USA-CA-Thousand Oaks
Technical Writer - Quality or document control, Medical Device or regu
Technical Writer - Quality or document control, Medical Device or regu
Thousand Oaks, California - USD
Unspecified
Posted:
Wednesday, 5 December 2018
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Job Description:
Looking for a Document Management Specialist for development of regulated or process documents with the
The quality control aseptic coaches are expected to be on the floor, in real time, observing and coaching aseptic operators in proper aspeticc technique.
Individuals need to have experience and knowledge of the aseptic environment and proper asepti
Lead Training Support for CCV PMSR Project and Integrate with PRISM Project
Finalize training plan
Develop learning objectives and design curriculum for effective adult learning for a global organization
Training strategy
Training needs ass
Collaborate with preclinical scientists across research units (Immunology & Inflammation, Internal Medicine, Rare Disease, CTI) to design, analyze and present experiments.
Bring innovative statistical thinking and methods to help drive the enhanced quantitative dru
Dec 08,2018
USA-CA-Los Angeles
Head of Site Capital Engineering - Los Angeles
Head of Site Capital Engineering - Los Angeles
Los Angeles, California
Unspecified
Posted:
Saturday, 8 December 2018
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Leads & Executes projects according to engineering and project management requirements. Leads & executes projects according to Sh
Dec 04,2018
USA-CT-Farmington
Supervisor Lead
Description Westaff is looking for a Production Warehouse Floor Lead for 2nd shift to\u00a0 work side by side with the Production Warehouse floor Supervisor and coordinates, organizes and monitors the receiving, storage, distribution and return of materials (including but not limited to raw mat
Leads & Executes projects according to engineering and project management requirements. Leads & executes projects according to Shire internal requirements fulfilling internal quality/compliance requirements.
Essential Duties an
Dec 10,2018
USA-FL-Orlando
Pharmacy Shipping Coordinator
Our client is seeking an individual to work under general supervision, the Shipping Coordinator is responsible for pack out of individual patient orders in shipping containers appropriate to stability requirements of drugs and creating accompanying FedEx shipping labels. Responsibilities: Performs o
Technician Pharmacy Jobs
