What are the responsibilities and job description for the Senior Development Scientist, Oral Solid Dose position at SRG?
Senior Development Scientist - Oral Solid Dose (OSD)
Location: Richmond, VA
Shape the future of oral solid dose products. We're looking for a Senior Development Scientist to lead formulation design, scientific experimentation, and scale-up for our OSD portfolio - driving innovation from lab bench to manufacturing floor.
About the Role
As Senior Development Scientist on our Oral Solid Dose (OSD) development team, you'll drive formulation design, rigorous scientific experimentation, scale-up, and technical risk assessment for existing OSD products. You'll bring strong expertise in formulation science, material characterization, and process understanding - translating laboratory insights into scalable, robust manufacturing processes. This role serves as a scientific leader for OSD projects, ensuring our products meet the highest standards of quality, performance, manufacturability, and regulatory compliance.
What You'll Do
- Lead formulation design and development using principles of scientific rigor, Quality by Design, and material science
- Develop prototypes, optimize formulations, and establish a Design Space through structured experimentation
- Evaluate interactions between API, excipients, and process parameters, translating that understanding into robust formulation strategies
- Develop Direct Compression, wet and dry granulation, and continuous manufacturing formulations based on project needs
- Plan, execute, and interpret Design of Experiments (DoE) to understand critical material attributes and critical process parameters
- Apply root cause analysis to resolve formulation and process failures
- Perform or interpret key characterization of raw materials and blends, including PSD, microscopy, rheology, compatibility, moisture sorption, and compressibility
- Design scalable manufacturing processes and partner with site technical teams on knowledge transfer
- Prepare technical protocols, reports, and regulatory documentation (CMC Module 3)
- Partner with Analytical, Quality, and Regulatory teams to ensure end-to-end technical alignment
- Present at internal R&D forums and external meetings
- Independently develop and communicate conclusions and recommendations for next steps
- Keep matrix leaders informed of progress and activities
What You'll Bring
Required:
- Bachelor's degree in Pharmacy or Life Sciences
- 5 years of relevant experience
Preferred:
- Master's, PhD, or equivalent practical experience in a relevant discipline
- Knowledge of regulatory requirements and the drug development process
- Strong problem-solving and scientific expertise
- Project management experience
- Experience analyzing data
- Ability to influence and collaborate across teams
Impellam Group and its brands are equal-opportunity employers committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, pregnancy or maternity, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application, interview process, pre-employment activity, and the performance of crucial job functions.
If you require additional disability considerations, modifications, or adjustments please let us know by contacting HR-InfoImpellamNA@impellam.com or fill out this form to request accommodations.
Salary : $50 - $54