Formulation Development Scientist - Oral Solid Dosage

Eurofins Scientific•Cambridge, MA

35d•$90,000 - $99,000•Onsite

About The Position

This scientist will develop formulations for oral solid dosage forms (tablets and capsules) on high-priority programs with accelerated timelines. Key responsibilities include designing and executing formulation and process development experiments, interpreting scientific data, and communicating findings to stakeholders. The role requires close coordination with cross-functional teams to meet tight project deliverables and authoring technical reports and CMC sections for regulatory submissions.

Requirements

A degree in chemistry, biology, pharmacy, engineering, or a related pharmaceutical science with at least 4 years of formulation development experience
BS with at least 6 years of industry experience, MS with at least 4 years of industry experience, or PhD with at least 6 months of industry experience in formulation development
Must have experience specificially with oral solid dosage formulation development
Strong knowledge of CMC pharmaceutical development, including hands-on operation manufacturing equipment and laboratory instruments (compression, wet/dry granulation, capsule filling, etc.)
Sound knowledge of current Good Manufacturing Practices
Technical writing experience
Experienced working in a multi-disciplinary team environment
Must be eligible to work in the United States indefinitely without restriction or sponsorship

Responsibilities

Understand project timelines and deliverables and plans/coordinates project work accordingly with stakeholders.
Contribute significantly and independently to project work which may include multiple projects within functional area.
Review, interpret and communicate data within project teams.
Plan and implement resolutions to technical problems/issues.
Independently design and execute experiments and report results.
Proactively analyze manufacturing issues and coordinate potential resolution with the drug substance team.