Teva Bioprocess Associate Post Vacancy – Biotechnology Jobs
Teva Bioprocess Associate Post. Teva invites postgraduate Biotechnology candidates for the post of associate. Associate post vacancy at Teva Pharmaceuticals. Job Opening at Teva. Biotech jobs in West Chester, Pennsylvania, US. Interested candidates may check out all the relevant details on the same below:
Job Title: Bioprocess Associate
Location: West Chester, Pennsylvania, US
Qualifications for Bioprocess Associate Post
- MS in Biotechnology with at least 1 year of downstream biologics process development experience
- In-depth understanding and hands-on experience in downstream unit operations like process chromatography in bind and elute as well as flowthrough mode, virus reduction filtration, ultrafiltration/diafiltration, etc
- Experienced in using AKTA chromatography systems (both lab and process-scale) and UNICORN software
- Experienced in using normal flow and tangential flow filtration skids
- Good understanding of process development and cGMP operation
- Knowledge of protein characterization methods and analytical techniques
- Excellent verbal and written communication skills required
- Highly motivated individual with the ability to work collaboratively in a team environment
Job Description
- Develop a stage-appropriate downstream process for Teva’s biologics pipeline and generate material for formulation development and toxicology study
- Evaluate new purification technologies to improve the efficiency of the biologics manufacturing process and reduce the cost of good
- Design fit-for-purpose purification experiments according to the stage of development, execute the runs in the process development lab, analyze performance data and write technical reports and prepare a presentation for management update
- Critically analyzes complex data, interprets and integrates experimental results with project objectives and write technical reports in timely manners
- Interact cross-functionally with Upstream process development, Drug Product,
- Analytical, Facilities, Quality Control, and other internal and external functions to support successful process development
- Support cGMP clinical manufacturing campaigns in Biologics Manufacturing Facility as needed
- Expands the technical capabilities of the Process Development group, by offering expertise in areas such as technology development, platform development, or using a literature precedent
