Scientist III
Confirmed on the employer's own hiring board on Nov 8, 2026. First seen by Alion on Nov 5, 2026. Planet Pharma scores B on the Alion truth index.
Target PR Range: 42-52/hr
*Depending on experience
Purpose:
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.