Process Development Associate II, Upstream at Abzena Inc. – San Diego, California
Abzena Inc.
San Diego, California, 92101, United States
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About This Position
Process Development Associate II, Upstream
With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing.
Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely.
We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services.
We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient.
The Associate II performs process development activities in collaboration with other individuals and departments to devise scalable and robust processes on accelerated timelines.
Qualifications- BS or MS degree in biological sciences, biotechnology, biochemistry or related fields with 3+ or 2+ years’ experience, respectively, in the pharmaceutical or biotechnology fields.
- Strong knowledge of mammalian cell cultures and concepts of cell metabolism, protein production, and characterization.
- Strong knowledge of cell culture process steps including cell banking, thaw and expansion, production (batch-fed and perfusion), and harvest.
- Skilled in operating ambr250 and STRs (2 L, 50 L, and 200 L); Sartorius STR experience preferred.
- Strong knowledge and skill in using equipment for determining cell counts and cell metabolism.
- Strong knowledge and experience with single-use technologies.
- Strong knowledge of quantitative and qualitative analytical methods and interpretation of analytical data.
- Skilled in data management.
- Skills in problem-solving and troubleshooting.
- Ability to follow instructions and to maintain accurate records and notes to write detailed development reports.
- Practical experience of cGMP manufacturing operations and fluency of regulatory regulations is desired.
- Comfortable in a fast-paced environment with minimal direction and able to adjust workload based upon changing priorities.
- Ability to work effectively in a team environment and motivated to work on multiple and various tasks, when required.
- Skill with Microsoft Office suite.
- Ability to safely operate production equipment in accordance with established practices.
FLSA: Non-Exempt
Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.
This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.
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Job Location
San Diego, California, 92101, United States
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