Scientist III

Reference: 632260Posted: 2026-11-04Location: North Chicago, IllinoisCompany: Planet Pharma GroupContact: ApplicationsEmail: View email address on click.appcast.io PR Range: 42-52/hr

• Depending on experiencePurpose:Biologics Drug Product Development (Bio DPD), a part of Development Sciences within R&D, is a global organization that is responsible for drug product formulation and process development, and definition of the product presentation for biologics and genetic medicine (proteins, conjugates, peptides etc.). Seeking a highly motivated candidate for the position of Scientist III, Biologics Drug Product Development, located in North Chicago, IL. We are seeking an accomplished scientist with a proven track record in biologics formulation and process development, and characterization.Responsibilities:* Lead the design and execution of biologics drug product formulation and process development, characterization and robustness studies.
• Support scale-up and technology transfer activities to internal and external manufacturing sites.
• Keep abreast of the latest advances in biologics formulation and process technologies.
• Effectively and timely communicates study plans, risks and mitigation plans to stakeholder and line management.* Understand relevant scientific literature and apply theoretical framework to solving problems within scientific discipline in a timely manner.
• Responsible for compliance with all applicable Corporate and Divisional policies and procedures.
• Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.Qualifications:
• Proven ability to solve critical scientific problems.
• Hands-on experience with biologics formulation development .
• Hands-on experience with analytical and biophysical characterization of proteins and solid-state characterization methods.
• Solid understanding of biologics degradation mechanisms and stabilization strategies.
• Hands-on experience with Design of Experiments (DoE), multivariate statistical analyses and data visualization tools. * Understanding of relevant cGMP and regulatory guidance.
• Experience with sterile manufacturing unit operations (freez-thaw, mixing, filtration, filling, and lyophilization) development, characterization, scale-up and technology transfer.
• Experience with quality risk management and drug product control strategies.Experience Level:
• Bachelors, Masters, or PhD in pharmaceutics, pharmaceutical sciences, chemistry, chemical engineering, or related disciplines with 8+ (Bachelors), 6+ (Masters), or 0+ (PhD) years of relevant industry experience.