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Scientist II, Biologics Drug Product Development

Company Description

  • Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
  • We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.

 

Job Description

Job description:

The Biologics Drug Product Development team develops antibody drug conjugates (ADC) and other biologics by state-of-the-art formulation and analytical technologies. We create valuable intellectual property through new formulation compositions, cost effective manufacturing processes and prepare and defend CMC (Chemistry, Manufacturing and Control) regulatory content. We are looking for a highly motivated person to support Developability and Formulation Development. The candidate will support early-stage assessment of candidates coming out of the Discovery pipeline, as well as the design and development of stable and robust drug product formulation for biologics used in clinical trials. In this role, the candidate will be part of a global team and will work closely with scientists from multiple functional areas, including Discovery, Analytical, and Process R&D.

Responsibilities:

  • Support the biologics characterization and stability assessment activities of the assigned biologics, including candidate screening and selection for clinical studies and commercialization of monoclonal antibodies, antibody drug conjugates, bispecifics, and fusion proteins.
  • Execute studies evaluating the stability (chemical & physical) of biologics against solution conditions (pH, ionic strength, temperature, light, etc.) and physical stresses arising from manufacturing process conditions (freeze thaw, mixing, filtration, filling, and lyophilization), and screen excipients (buffers, stabilizers, surfactants, etc.) to develop robust formulations for frozen, refrigerated liquid, and lyophilized dosage forms.
  • Prepare concise and sound scientific presentations of experimental results to the management and assist in authoring detailed scientific technical reports.
  • Stay current with the scientific literature and support new scientific initiatives.

Requirements:

  • BS or MS in a scientific field and typically 4 (BS) or 2 (MS) years of relevant experience.
  • Extensive hands-on expertise using analytical methods for chemical and structural characterization of biologics e.g. HPLC, UPLC, capillary electrophoresis, particle analysis, and other biophysical techniques (UV-vis, DLS, DSC, etc.) for protein characterization is a requirement.
  • Scientific understanding of the structure & function of monoclonal antibodies, antibody constructs/conjugates, bispecifics, and fusion proteins and their modes of degradation/stabilization.
  • Strong laboratory skills focused on formulation development for monoclonal antibodies and antibody constructs/conjugates (standard excipient selection, functional excipients, high throughput assays).
  • Solid understanding of the various unit operations of aseptic manufacturing such as bulk freeze thaw, compounding/mixing, filtration, filling, and lyophilization for liquid and lyophilized NBEs.

Key Competencies:

  • Builds strong relationships with peers and cross functionally with partners outside of the team to enable higher performance.
  • Excellent oral communication skills in a scientific setting, as well as sound technical writing and documentation competencies are required.
  • The candidate must be able to work independently, respond to changing priorities and short lead times for multiple tasks; able to identify problems and work toward solutions.
  • Raises the bar and is never satisfied with the status quo.
  • Creates a learning environment, open to suggestions and experimentation for improvement.
  • Embraces the ideas of others, nurtures innovation and manages innovation to reality.

Additional Information

All your information will be kept confidential according to EEO guidelines.

Average salary estimate

$80000 / YEARLY (est.)
min
max
$70000K
$90000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About Scientist II, Biologics Drug Product Development, Katalyst Healthcares & Life Sciences

At Katalyst Healthcares & Life Sciences, we are on the hunt for a dedicated Scientist II in Biologics Drug Product Development to join our exceptional team based in Antioch, IL. As part of our Biologics Drug Product Development team, you'll play a key role in developing cutting-edge antibody drug conjugates (ADC) and other biologics using state-of-the-art formulation and analytical technologies. Your contributions will help shape new formulation compositions and efficient manufacturing processes, all while ensuring compliance with Chemistry, Manufacturing and Control (CMC) regulatory standards. In this fascinating role, you'll be deeply involved in the development and characterization of biologics for clinical trials. Your responsibilities will include assessing the stability of various biologics and executing rigorous studies that evaluate their durability under a variety of conditions. Collaborating with scientists across Discovery, Analytical, and Process R&D, you'll support the successful selection and screening of candidates for clinical studies. If you're passionate about pushing boundaries in pharmaceutical science and making a difference in patients' lives, this position at Katalyst is an exciting opportunity to grow and innovate in the world of biologics.

Frequently Asked Questions (FAQs) for Scientist II, Biologics Drug Product Development Role at Katalyst Healthcares & Life Sciences
What responsibilities does a Scientist II in Biologics Drug Product Development at Katalyst Healthcares & Life Sciences have?

The Scientist II in Biologics Drug Product Development at Katalyst Healthcares & Life Sciences is responsible for supporting the biologics characterization and stability assessments, executing studies that evaluate the stability of biologics under various conditions, and screening excipients to develop robust formulations. Additionally, they prepare scientific presentations of experimental results and author detailed technical reports.

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What qualifications are needed for the Scientist II position in Biologics Drug Product Development at Katalyst?

Candidates for the Scientist II position at Katalyst must possess a BS or MS in a scientific field with relevant experience, typically four years for a BS or two years for an MS. Hands-on expertise in analytical methods for characterizing biologics, as well as an understanding of monoclonal antibodies and their degradation modes, is crucial.

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What skills are essential for a Scientist II at Katalyst in the field of Biologics Drug Product Development?

Key skills for a Scientist II in Biologics Drug Product Development at Katalyst include strong laboratory expertise in formulation development, excellent oral and written communication skills, and the ability to work independently and collaboratively within a team. Additionally, insight into aseptic manufacturing operations is highly beneficial.

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How does the Scientist II position at Katalyst contribute to clinical trials?

The Scientist II contributes to clinical trials at Katalyst by supporting the early-stage assessment of biologics candidates from the Discovery pipeline. This role is crucial for designing and developing stable and robust drug product formulations that will be evaluated in clinical studies.

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What type of environment does Katalyst Healthcares & Life Sciences provide for a Scientist II in Biologics Drug Product Development?

Katalyst provides a dynamic and supportive environment that fosters innovation and collaboration. As a Scientist II, you'll have the opportunity to work with talented individuals across various scientific disciplines, encouraging a culture of learning and experimentation for continuous improvement.

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Common Interview Questions for Scientist II, Biologics Drug Product Development
What experience do you have with the characterization of biologics?

When responding to this question, highlight your hands-on experience with various analytical methods used in biologics characterization, such as HPLC and UPLC. Discuss specific projects where you've successfully applied these methods to evaluate the stability or quality of biologics.

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How do you approach formulation development for biologics?

In your answer, describe your systematic approach to formulation development, including candidate screening, stability assessments, and excipient selection. Provide examples that showcase your problem-solving skills and your ability to create robust formulations.

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Can you discuss a challenging problem you faced in a previous role and how you resolved it?

Answer this by outlining a specific challenge related to biologics formulation or characterization. Explain the steps you took to investigate and resolve the issue, emphasizing your analytical thinking and collaboration with your team.

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How do you stay current with advancements in biologics and drug formulation?

Share your strategies for keeping up with the latest research and scientific literature. Mention subscriptions to relevant journals, participation in conferences, and any professional organizations you are a part of.

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What role do you believe communication plays in a laboratory team?

Discuss the importance of clear and effective communication in ensuring that all team members are aligned on project goals, methodologies, and results. Provide examples of how you've successfully communicated complex information to both scientific and non-scientific stakeholders.

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Describe your experience with CMC regulatory content preparation.

Talk about your familiarity with Chemistry, Manufacturing, and Control regulatory requirements. Discuss any experience you have in preparing CMC documentation and how you ensure compliance while developing biologics.

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How do you prioritize tasks in a fast-paced research environment?

Explain your method for prioritizing tasks effectively, how you manage deadlines, and ensure that critical experiments are completed efficiently. Discuss any tools or techniques you utilize to stay organized.

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What analytical techniques do you find most useful in biologics product development?

Detail the analytical techniques you find most valuable, such as DLS, UV-Vis spectroscopy, or particle analysis, and explain how you apply them in your work to ensure the quality of biologics.

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What excipients do you think are most important for protein stabilization?

Discuss various excipients such as buffers and stabilizers that you believe play critical roles in protein stabilization. Provide insights into your experience selecting functional excipients for formulation development.

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How would you handle a situation where experimental results do not meet your expectations?

Describe your strategy for troubleshooting unexpected results in experiments. Emphasize your analytical mindset, willingness to investigate, and the importance of documenting findings for future learning.

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MATCH
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SENIORITY LEVEL REQUIREMENT
TEAM SIZE
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HQ LOCATION
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EMPLOYMENT TYPE
Full-time, on-site
DATE POSTED
March 27, 2025

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