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Scientist II, Biologics Drug Substance Development, Cell Culture Development

AbbVie

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AbbVie

Scientist II, Biologics Drug Substance Development, Cell Culture Development

Onsite South San Francisco, CA, United States Full Time
Posted 20 hours ago
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powertofly approved What AbbVie Has to Offer:

Our work can—and does—have a tangible, lasting impact on millions of people. But it’s not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.

Job Details


Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.


Job Description

The Cell Culture Development Group in South San Francisco, CA is seeking a Scientist II to join a talented and collaborative team to develop cell culture processes for GMP applications.

In this position, you will perform cell culture process development, scale-up, and technology transfer activities in a well-supported and dynamic environment to help advance novel biotherapeutics into human clinical studies.

KEY RESPONSIBILITIES:

· Develop and optimize robust and scalable cell culture processes in ambr250 and 2L bioreactors

· Perform pilot scale material generation using 50L, 200L and 500L single use bioreactors

· Develop inoculum expansion and master cell bank generation processes

· Design and execute small scale and pilot scale depth filtration and centrifugation primary recovery processes

· Perform tech transfer of Master cell bank generation, cell culture and primary recovery processes to the GMP manufacturing facilities

· Provide person-in-plant support at the GMP manufacturing facility

· Develop and optimize N-1 perfusion processes as well as intensified fed-batch processes

· Represent the cell culture development group in cross-functional meetings and collaborate closely with cell line, purification, analytical and formulation development leads to meet project timelines

· Author and review technical reports, GMP campaign summary reports and relevant sections in regulatory filings

· Proactively identify and implement opportunities to optimize platform processes and deepen process understanding

· Present scientific findings at internal or external conferences


Qualifications

Basic:

· Scientific degree in chemical engineering, bioengineering, biotechnology, or a related field, ≥ 5 years for M.S., or ≥ 7 years for B.S.

· Proficient in aseptic techniques

· Experienced in developing and executing mammalian suspension cell culture processes in shake flasks, ambr250 and 2L bioreactors

· Significant experience with perfusion technology, especially Alternating Tangential flow filtration (ATF) at bench and pilot scale

· Strong understanding of mammalian cell and molecular biology and cell culture bioprocess engineering concepts

· Strong attention to detail; active and quick learner; able to change courses quickly as needed, raises the bar and is never satisfied with the status quo; open to suggestions and embraces the ideas of others; collaborative actively builds relationships with others

· Experienced in technical report authoring and reviewing

· Proficient with Microsoft Office software (Word, Excel, and PowerPoint) and statistical modelling software such as JMP

Preferred:

· Experience with authoring peer-reviewed publications, technical reports, regulatory documents, and/or presentations at conferences

· Basic knowledge of automation and coding languages (Python, etc.)


Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​

  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time ofthis posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location,and we may ultimately pay more or less than the posted range. This range may be modified in the future. ​

  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​

  • This job is eligible to participate in our short-term incentive programs. ​

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of anybonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's soleand absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. 

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Company Details
AbbVie
 Chicago, IL, United States
Work at AbbVie

Together, we break through We believe the paths we take to achieving our breakthroughs matter. At AbbVie, every one of our 50,000 employees is a... Read more

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