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Scientist I/II, Biologics Upstream Process Development

Our mission at Asimov is to advance humanity's ability to design living systems, enabling biotechnologies with outsized benefit to society. We're developing a mammalian synthetic biology platform––from cells to software––to enable the design and manufacture of next-generation therapeutics.


We are seeking a Scientist I/II, Biologics Upstream Process Development to join our team in Boston, MA and help push the boundaries of biopharmaceutical and gene therapy process development. This role is for a technical expert who will conduct bioprocess engineering for biologics, design complex experimental approaches to improve our workflows and systems, apply scaling principles to upstream processing, and coordinate interdepartmental project efforts.

 

The successful candidate will work closely with Asimov’s synthetic biology, cell line development, and analytical development teams, along with interfacing with external partners. The role reports to the Head of Process Development and is a unique opportunity to work at a nimble, forward-thinking synthetic biology startup and help build the future of biological engineering.


About the Role:
  • You will be involved hands-on in projects that include media/feed optimization, bioreactor process development, process scale-up and characterization at Ambr15, Ambr250, and benchtop scale (2L/10L).
  • Serve as a technical subject matter expert (SME) in upstream process development for both internal and external projects.
  • You will represent the process development team on cross-functional projects, making decisions for process development activities and effectively communicating results, progress, and plans.
  • Work together with the strategic alliance and commercial teams to technology transfer developed upstream processes to external partners.
  • Collaborate with internal process modeling team to test hypotheses for developing robust predictive models using DOE approaches, machine learning algorithms, and multi-omics analysis.
  • Collaborate with the software team to develop integrated data platforms and analysis for streamlined data analysis.
  • Author, review, and approve process development reports and technology transfer protocols.
  • Organize and document experiments and data in an electronic lab notebook.
  • Perform clarifications, downstream processing/purification, and product quality assessment with analytical tools when needed.


About You:
  • You have a PhD in Biological Engineering, Chemical Engineering, Cell Biology, Molecular Biology, or a related field with 0-2 years of relevant hands-on experience in bioprocessing. Alternatively, a MS with minimum of 4 years or a Bachelors with minimum 6 years of hands-on industry experience.
  • You are a creative problem solver and get excited about the opportunity to drive the creation of industry-disruptive technology.
  • Mammalian (CHO) process development is squarely in your wheelhouse. Experience with LVV and AAV process development is beneficial but not essential.
  • Experience with “-omics” (i.e., metabolomics, proteomics, glycomics) and impact on drug product quality attributes is a plus.
  • You have experience with Ambr15, Ambr250, and/or benchtop scale fed-batch bioreactor (WAVE, STR) processes. Perfusion experience is welcomed but not required. Analytical development and downstream purification experience (i.e., TFF) is also highly preferable.
  • Being detail-oriented is not just a sound bite for you, it is part of your DNA. Keeping track of a bunch of moving parts is easy for you because you are highly organized. It is not your first time following a standardized workflow or pipeline.
  • Experience in the technology transfer of manufacturing processes and CMC filing in the pharmaceutical industry is required.
  • You are an expert in spreadsheets such as Google Sheets or Excel and ideally Spotfire, Google Apps Script (JavaScript) and/or BigQuery to facilitate data management and analysis.
  • Experienced using DOE software to develop robust experiments. Familiarity with implementing algorithm-based design approaches is a plus.


We're fueled by a vision to transform biological engineering into a fully-fledged engineering discipline. Should you join our team, you will grow with a constantly evolving organization and push the frontiers of synthetic biology. Company culture is key to Asimov, and ours is a culture of recombination; we believe that our mission can only be achieved by bringing together a diverse team with a mixture of backgrounds and perspectives.

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What You Should Know About Scientist I/II, Biologics Upstream Process Development, Asimov

At Asimov, we're on a mission to empower humanity to design living systems that deliver extraordinary benefits to society through innovative biotechnologies. We're excited to welcome a Scientist I/II in Biologics Upstream Process Development to our vibrant team in Boston, MA. This unique opportunity is for a technical aficionado who thrives at the intersection of science and creativity, keen to explore biopharmaceutical and gene therapy process development. In this role, you’ll dive into hands-on projects involving media/feed optimization and bioreactor process development, utilizing Ambr15, Ambr250, and benchtop scales. As the go-to expert in upstream process development, you’ll not only engage with internal teams but also bridge connections with our external partners. Your contribution will be vital as you author and review development reports, coordinate cross-functional projects, and implement predictive models while collaborating with our software team to streamline data analysis. If you possess a PhD or MS in a related field and have a strong foundation in mammalian process development, this could be the perfect place for you to thrive. You’ll be working with a dedicated team of innovators who are passionate about pushing the frontiers of biological engineering. Join us in shaping the future, where your talent can make a significant impact!

Frequently Asked Questions (FAQs) for Scientist I/II, Biologics Upstream Process Development Role at Asimov
What are the key responsibilities of a Scientist I/II in Biologics Upstream Process Development at Asimov?

As a Scientist I/II in Biologics Upstream Process Development at Asimov, your primary responsibilities include engaging in hands-on projects, conducting media/feed optimization, and leading bioreactor process development. You will be involved in process scale-up efforts and collaborate closely with cross-functional teams to ensure effective communication and project advancement.

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What qualifications are required for a Scientist I/II at Asimov?

Candidates for the Scientist I/II role at Asimov should hold a PhD in Biological Engineering, Chemical Engineering, Cell Biology, or related fields, or possess a Master’s with at least four years of experience or a Bachelor’s with six years of hands-on industry experience. Experience in mammalian process development and analytical tools is essential.

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How does teamwork function for the Scientist I/II position at Asimov?

Teamwork is a cornerstone of the Scientist I/II position at Asimov. You will coordinate with various departments, including synthetic biology, analytical development, and commercial teams, ensuring that upstream processes are successfully transitioned to external partners while leveraging diverse insights to enhance project outcomes.

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What kind of projects will a Scientist I/II work on at Asimov?

As a Scientist I/II in Biologics Upstream Process Development at Asimov, you will work on projects that involve media/feed optimization, process development in bioreactors, and the science of scaling up these processes. You will also collaborate on creating predictive models using advanced data analysis techniques.

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Is prior experience in technology transfer important for the Scientist I/II role at Asimov?

Yes, prior experience in technology transfer of manufacturing processes and CMC filing is crucial for the Scientist I/II position at Asimov. It ensures that you can effectively contribute to the transition of upstream processes developed in-house to our external partners.

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Common Interview Questions for Scientist I/II, Biologics Upstream Process Development
Can you explain your experience with upstream bioprocessing technologies?

To effectively answer this question, highlight specific technologies you’ve used, such as Ambr150 or Ambr250. Discuss projects you’ve worked on, the results achieved, and how your experience can contribute to Asimov's goals.

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How do you approach media and feed optimization in bioreactor processes?

You can answer by describing your systematic approach to media optimization, including parameters you analyze, the impact of different media components on cell growth, and examples from past projects that illustrate successful optimization.

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What strategies do you use to collaborate with cross-functional teams?

Discuss your communication techniques, tools you utilize like project management software, and examples where your collaboration has led to successful outcomes. Emphasize the importance of shared goals.

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Describe a time when you encountered a challenge during an experiment and how you resolved it.

Think of a specific example where you faced a difficult situation, communicate your thought process, the steps you took to troubleshoot, and the lessons learned from it.

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What are the important quality attributes of biologics that you consider during process development?

Focus on stability, efficacy, safety, and consistency. Explain how you ensure these attributes are preserved through process development stages and what tools or methodologies you use.

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What experience do you have with analytical tools used in downstream purification?

Share your experience with specific tools like TFF, HPLC, or FPLC, and discuss how you have employed them in past roles to assess product quality parameters.

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How do you document and organize your experiments in the lab?

Detail your use of electronic lab notebooks and your structured approach to documenting protocols, data, and outcomes to ensure reproducibility and clarity.

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What role does data analysis play in your work, and what tools do you use?

Discuss the significance of data analysis in bioprocessing and tools that you have experience with, such as Google Sheets, Spotfire, or statistical software, emphasizing your ability to interpret and visualize data effectively.

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How familiar are you with design of experiments (DOE) methodologies?

Outline any previous experiences employing DOE, mentioning specific projects where these methodologies improved your results, emphasizing your analytical skills in designing robust experiments.

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Why do you want to work at Asimov and in this specific role?

Articulate your passion for synthetic biology and your admiration for Asimov’s mission. Connect your skills and experiences to the role, expressing how you envision contributing to the team.

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Full-time, on-site
DATE POSTED
December 15, 2024

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