• Full Time
  • Bend, OR
  • Dec 31, 2022

Website Lonza

Lonza Pharma & Biotech has an opening for a Scientist III on the Product Development team. A successful Scientist must be sound in fundamental scientific knowledge and methods, proficiently execute a wide range of techniques and processes with little supervision, demonstrate effective technical writing, and be a leader and mentor in the laboratory environment.


Key Responsibilities:

Recognized expert in laboratory techniques and instrumentation relevant to technological focus
Demonstrate an advanced understanding of at least one fundamental discipline (1) with functional proficiency in all
Select appropriate models for data analysis and understand underlying derivation
Demonstrate an advanced understanding of transport phenomena and process engineering
Independently acquire knowledge to solve new problems
Mentor and provide feedback to peers and Scientist I/II
Successfully prioritize and manage multiple program deliverables across several phases of development (discovery through clinical) and consistently delivers with high scientific quality and on time
Document and communicate design and outcomes (both written and verbal) to the internal project team and the client without supervision
Assist in defining strategy for projects/programs
Draft and edit complete drafts of client documents that are ready to send with little input/revision
Interface with colleagues broadly and proactively throughout the organization/site to achieve goals
Demonstrate familiarity with experimental instrumentation and techniques outside of technological focus
Support GMP analytical and manufacturing activities as necessary serving as the SME on risk assessments, investigations, and troubleshooting on methods or materials
Perform other duties as assigned
Key Requirements:

B.S./M.S. with experience relating to pharmaceutical formulation development and analytical chemistry
Experience with analyzing, and interpreting common analytical data used for amorphous pharmaceutical applications such as dissolution, GC, XRPD, HPLC, KF and particle sizing
Experience in method development, qualification and validation around common pharmaceutical analytical techniques
Knowledge of CMC (Chemistry, Manufacturing and Controls) and regulatory experience with advancing drug product formulations through later stage clinical trials encouraged
Demonstrated ability to work successfully in a highly collaborative, team oriented, customer focused environment
Must possess excellent verbal and written communication skills and ability to work in a dynamic, multi-disciplinary, research and manufacturing environment
Promote safety and demand high quality standards for work being performed

To apply for this job please visit lonza.wd3.myworkdayjobs.com.