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R&D Associate I / R&D Associate II MD
2/11/2016 7:18 AM

The R&D Associate I/II will be required to document assay data in a GxP manner, analyze test data, interpret results and complete a variety of sample testing within established timelines. This role will include training on new assays and new equipment as tranfers occur between the group and internal/external partners. The chosen candidate will be responsible for follwing the AZ code of conduct whe  ...View Job
Associate QC Scientist MD
2/10/2016 6:28 AM

* Performs routine testing for release, stability and in process samples. * Drives the implementation of new technology. *Provides technical guidance for lower level personnel * posesses broad instrument and theoretical knowledge of multiple specialized analytical areas (e.g. HPLC, CGE, cIEF, UPLC, bioanalyzer) * Serves as QC interface with internal and external customers. * Provide  ...View Job
Manager, Mfg. & Process Safety MD
2/10/2016 6:28 AM

Implement and manage SHE programs within Biopharmaceutical Development to protect personnel and the environment, maintain compliance, and minimize business risks with direct support to the Gaithersburg Pilot Facility, Development Scale-Up, Quality Assurance, and Quality Control at MedImmune's Gaithersburg campus. Major Responsibilities: Utilize Behavioral Safety Program within Biopha  ...View Job
Business Analyst - PMO CO
2/10/2016 6:28 AM

Supports AstraZeneca's Operations' Boulder Manufacturing Center (BMC) site projects, project execution processes and project reporting including PMO-based operational excellence projects. Interfaces with project team members to ensure effective project administration and reporting. Supports all site project, BMC portfolio management and governance processes. Reports to the Project Management depar  ...View Job
Senior Manager Manufacturing CO
2/10/2016 6:28 AM

Manage and lead the Upstream production area of a biological manufacturing process. Knowledgeable of the current Code of the Federal Regulations (CFR's) and Current Good Manufacturing Practices (cGMP's) Manage production operations, with emphasis on safety and quality to on-time delivery of biologics to supply plan Investigate and resolve problems, and identify and implement process impro  ...View Job
Sr. Manager - Manufacturing CO
2/10/2016 6:28 AM

Manage and lead the Downstream production area of a biological manufacturing process. Knowledgeable of the current Code of the Federal Regulations (CFR's) and Current Good Manufacturing Practices (cGMP's) Manage production operations, with emphasis on safety and quality to on-time delivery of biologics to supply plan Investigate and resolve problems, and identify and implement process imp  ...View Job
Production Tech II MD
2/9/2016 6:50 AM

* Manufactures clinical and commercial biologics meeting the regulatory requirements of both domestic and international markets * Experts and Qualified Trainers in the operation of production equipment in multiple areas in a large scale, automated bioprocess plant such as, bioreactors, centrifuges, virus filtration, depth filtration, tangential flow filtration, chromatography equipment, washers  ...View Job
QC Analyst/Sr. QC Analyst MD
2/8/2016 6:52 AM

Performs selected quality control testing activities, dependent upon assigned area, including the following: * Responsible for conducting in process, finished product and stability testing according to standard operating procedures. * Completes appropriate documentation supporting testing procedures, including data capture forms, equipment logbooks, and inventory forms. * Identifies and t  ...View Job
Scientist II - Validation MD
2/5/2016 6:48 AM

The Scientist II core responsibilities include designing validation sampling/test plans, performing development studies, generating validation protocols, executing validation studies, resolving technical issues encountered during study execution, and preparing validation final reports. This position independently plans, designs, and executes projects that are complex and scientifically demanding.   ...View Job
Scientist I - Validation MD
2/5/2016 6:48 AM

The Scientist I core responsibilities include designing validation sampling/test plans, performing development studies, generating validation protocols, executing validation studies, resolving technical issues encountered during study execution, and preparing validation final reports. This position conducts and participates in projects that are complex and scientifically demanding. This position h  ...View Job
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