Senior Development Scientist - Oral Solid Dose (OSD)

Hello,

I hope you're doing well.

My name is Uzma Kousar Mohammed, and I'm reaching out from Intellectt Inc. regarding an exciting contract opportunity for a Senior Development Scientist Oral Solid Dose (OSD) based in Richmond, VA with one of our prestigious clients.

I would love to connect and discuss this opportunity in more detail. Please feel free to share your updated resume at View email address on us.fitly.work

Role: Senior Development Scientist Oral Solid Dose (OSD)



Location: Richmond, VA Onsite



Rate: $40 - $45/hr on W2

Job Summary:

We are seeking a Senior Development Scientist with strong Oral Solid Dose (OSD) formulation experience to lead formulation development, scientific experimentation, scale-up, and process optimization from laboratory through manufacturing.

Key Responsibilities:

• Lead OSD formulation development using Quality by Design (QbD) and material science principles.
• Develop and optimize formulations using Direct Compression, Wet/Dry Granulation, and Continuous Manufacturing.
• Design and execute Design of Experiments (DoE) and establish formulation/process design spaces.
• Evaluate API, excipient, and process parameter interactions.
• Perform root cause analysis and troubleshoot formulation/process issues.
• Characterize materials and blends, including PSD, microscopy, rheology, moisture sorption, compatibility, and compressibility.
• Support scale-up, process development, and technology transfer to manufacturing sites.
• Prepare technical protocols, reports, and CMC Module 3 documentation.
• Collaborate with Analytical, Quality, Regulatory, and Manufacturing teams.
• Present scientific findings and provide technical recommendations to project leadership.

Required Qualifications:

• Bachelor's degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, or related field.
• 5+ years of relevant pharmaceutical development experience.
• Strong experience in OSD formulation and process development.
• Knowledge of QbD, DoE, material characterization, and scale-up.
• Strong scientific problem-solving, data analysis, and communication skills.

Preferred:

• Master's/PhD or equivalent practical experience.
• Knowledge of regulatory requirements and drug development/CMC processes.
• Project management and cross-functional collaboration experience.

Benefits: Eligible employees may have access to benefits offered by Intellectt Inc. in accordance with the applicable benefit plans and eligibility requirements.

Equal Employment Opportunity:
Intellectt Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, disability, genetic information, veteran status, or any other characteristic protected by applicable federal, state, or local law.

Thanks & Regards,
Uzma Kousar Mohammed
Technical Recruiter
Intellectt Inc


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