Scientist

Thousand Oaks, California | Contract

Post Date: 12/04/2017 Job ID: 3639 Industry: Biotech

Description:

 

Scientist responsibilities include, but are not limited to, the following: 
  • Independently execute experiments in order to characterize and enable implementation of new capabilities that advance state-of-the art automation, high throughput screening, formulation, filling, lyophilization and analytical technologies 
  • Serve as single point of contact and subject matter expert (SME) on complex capabilities. Enable walk-up utilization and own business process. 
  • Independently design and execute process development studies to characterize formulation, filling, lyophilization, capping, and inspection operations to deliver robust manufacturing processes and drug products 
  • Apply fundamental scientific (biochemistry, biophysics, statistics, etc.) and engineering principles to resolve issues and evaluate effects of process improvements, equipment, scale, and raw materials 
  • Conduct analysis of data generated from any of the above listed activities, including statistical analysis using SAS, JMP etc., and effectively communicate results 
  • Troubleshoot malfunctioning equipment, work with Lab Ops, Asset Management, Facilities and vendors to repair 
  • Author/review technical documents, such as technical protocols, technical assessments, technical reports, regulatory documents 
  • Perform tasks related to safety and compliance initiatives in the lab. 
  • Manage procurement and inventory levels of commonly used lab supplies and chemicals 

 

 

Preferred Qualifications: 
 
  • Displayed critical thinking, problem solving and independent research skills 
  • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies 
  • Good computer and organizational skills with strong attention to detail 
  • Excellent communication (oral and written) 
  • Excellent project management skills including the ability to manage project resource requirements (material, manpower, time, etc.), and ability to elevate relevant issues to project lead and line-management 
  • Self motivation, adaptability and a positive attitude 
  • Ability to work independently and as part of a team with internal and external partners 
  • Experience working in GMP environments or process development 

 

Qualifications: 
 

B.S. with 4? 6 years of industry experience, M.S. with 3? 4 years experience, with degree in Engineering

 
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