Duration: 12 months contract (possible extension – based on performance and business needs )
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.).
- Client is 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.
Top Skills Required:
- Hands-on experience with biologics formulation development .
- Hands-on experience with analytical and biophysical characterization of proteins and solid-state characterization methods.
- Experience with sterile manufacturing unit operations (freeze-thaw, mixing, filtration, filling, and lyophilization) development, characterization, scale-up and technology transfer.
- Proven ability to solve critical scientific problems.
- 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.
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com .
Equal Employment Opportunity (EEO): US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
AI Statement: By applying, you acknowledge that AI-assisted tools may be used during hiring.
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