Job Description
Job Summary:
- Client is seeking a highly motivated formulation scientist to join its Pharmaceutical Research Sciences department in Lexington, Massachusetts.
- The candidate will be responsible for the formulation and characterization of PEP Product, proteins, small molecules, and bioconjugates.
Duties and Responsibilities:
- Prepare PEP Product and protein injectable formulations for in vitro and in vivo studies including selection of buffers, excipients, surfactants and conducting the relevant biophysical characterization and stability studies
- Collaborate with cross-functional teams to ensure the selected dosage form meets the desired biophysical and biochemical profile and contribute to early screening strategies and execution
- Operate, maintain, and troubleshoot lab instruments such as biophysical and analytical characterization equipment
- Conduct laboratory work in a safe, efficient manner that ensures a safe working environment for colleagues
Education and Experience:
- Bachelor’s Degree required.
- Degree within subject matter expertise (biological, biochemical, or pharmacological sciences) preferred
- 2+ years’ relevant technical experience required.
- Experience in preparing injectable formulations for animal studies
- Experience in managing projects and working collaboratively with cross-functional teams.
- Experience with spectroscopy, calorimetry, light scattering, and other biophysical methods for PEP Product and protein injectable formulations is a plus.
Knowledge, Skills and Abilities:
- Highly communicative and able to quickly solve problems as they arise.
- Strong knowledge and expertise in biophysical characterization and injectable formulation development.
- Proficient in data analysis and interpretation for drawing conclusions and making recommendations.
- Excellent scientific communication skills and ability to engage with stakeholders effectively.
- Strong attention to detail and ability to document experimental work with electronic laboratory notebooks (ELN).
- General knowledge of cGMP, GLP, and regulatory requirements for pharmaceutical industries a plus.