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Associate Scientist, Process Development II


AbbVie Inc.


Location

South San Francisco, CA | United States


Job description

The Biologics CMC Development team at AbbVie in the Bay Area has a long and rich history of biologics development. Now located in a new state of the art facility in South San Francisco, the team leverages its comprehensive end-to-end CMC capabilities to work collaboratively through all phases of CMC development with a primary focus on advancing complex biologic therapies, such as bi-specifics and novel modalities, to human clinical studies and eventual licensure.  This Scientist I  role is within a team of highly experienced scientists and managers who have directly enabled the development/IND submissions of 20+ novel oncology drugs and successfully filed two BLAs.

As one of CMC purification development scientists, you will work in the CMC purification team to develop robust, phase-appropriate processes for drug substance GMP production to enable human clinical studies and eventual licensure. This position is an onsite role in a lab-based function. To be successful, candidates must enjoy and thrive in an onsite, highly collaborative lab environment with daily face-to-face interactions between scientists.

R esponsibilities include:

· Support development, optimization, and scale-up of purification processes through lab-based and pilot plant operation activities

· Support transfer of purification processes to GMP manufacturing for clinical material production

· Execute routine purification development operations from harvest to UF/DF operations competently and independently, and generate reliable and consistent results

· Analyze and critique experimental results, noting significant deviations

· Prepare small to large (500L) batches of buffer solutions following batch record recipe

· Support pilot plant activities including preparation and execution

· Perform routine analytical measurements using HPLC and UV-vis instrumentation

· Accurately record and manage multiple data sets and batch records in electronic notebooks, databases and excel files

· Perform general lab maintenance including cleanliness, equipment maintenance and maintaining inventory

· Collaborate within the team in order to follow best practices and meet project goals

· Be flexible to participate in innovative projects with shifting priorities and ambiguity in direction

· Learn and understand new experimental techniques

· Must be comfortable with physical activities of constant standing, walking, sitting and occasionally lifting up to 50Ibs

· Author technical reports and presentations including preparing verbal updates and presentations at group meetings

Basic:

· Bachelor’s Degree or equivalent education and typically 3 years of experience; MS or equivalent education and typically 0 years of experience

· Must have hands-on protein purification experience such as chromatography separations and filtration operations

· Experience with operating and programing methods for AKTA chromatographic instruments (such as AKTA Avant, AKTA Purifier, AKTA Pure or similar)

· Must have excellent attention to detail and ability to keep detailed written records

· Able to analyze and critique experimental results and note significant deviations

· Able to work collaboratively within and outside of the group

· Able to learn and understand new experimental techniques

· Has understanding of bioprocess engineering concepts

· Has strong planning and analytical skills

· Has strong interpersonal and communication skills

· Proficient in scientific writing skills and verbal communication including scientific data presentations

· Proficient in Microsoft Office software and have ability to learn new software applications

Preferred:

· Has hands on experience with purification development operations including harvest, depth filtration, virus inactivation, chromatographic membrane, polishing chromatography, virus filtration, and UF/DF operations

· Has hands on experience with monoclonal antibody or antibody-like molecule purification at GMP, pilot and/or laboratory bench scale

· Understanding of analytical techniques, such as HPLC, LAL, and ELISA

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

AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.


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