FSP Associate Scientist: Pharmaceutics, Solid Dosage Preparation
About The Position
The Associate Scientist will prepare solid dosage formulations, including blends, tablets, and capsules, independently or in collaboration with internal scientists in development and pilot plant laboratories. The role performs characterization of drug substances, excipients, intermediates, and finished formulations to assess material attributes and performance. Analyses include powder flow, bulk and tapped density, particle size distribution, compaction properties, tablet hardness and tensile strength, solid fraction, friability, disintegration, and solubility. The scientist reviews experimental data, identifies trends, and proposes hypothesis-driven follow-up experiments. The role requires documenting research in an electronic lab notebook according to departmental guidelines, complying with environmental health and safety requirements, completing required training, and communicating findings and technical recommendations to cross-functional teams in the Synthetic Molecule Pharmaceutics group. Work takes place in a laboratory and/or clinical environment. Conditions may include exposure to electrical office equipment, biological fluids and infectious organisms, and rare exposure to irritants, radiation, toxic materials, hazardous waste, or extreme temperatures. Required PPE includes protective eyewear, garments, and gloves. Occasional site drives and domestic travel may be required.
Requirements
- Bachelor's degree in chemistry, material sciences, pharmaceutical sciences, chemical engineering, or a closely related area.
- Experience providing the knowledge, skills, and abilities to perform the job, comparable to 0 to 1 years; an appropriate combination of education, training, and/or directly related experience may be considered equivalent.
- Proficiency in following complex, repetitive experimental protocols and batch records without deviation.
- Demonstrated proficiency in Microsoft Office, including Excel, Word, and PowerPoint, for documentation and data management.
- Excellent organizational skills and ability to maintain focus and quality during routine tasks while meeting deadlines under pressure.
- Clear written and verbal communication skills to record data accurately and report findings to project teams.
- Ability to work collaboratively in fast-paced settings and contribute to cross-disciplinary project teams.
Nice To Haves
- Knowledge and hands-on experience in powder processing, handling, and characterization.
- Strong background in applied mathematics and core engineering principles.
- Hands-on experience with solid dosage form development and powder characterization.
- Prior hands-on experience in a 100% laboratory-based operational environment.
- Alignment with the company’s values of Integrity, Courage, and Passion.
Responsibilities
- Prepare solid dosage formulations, such as blends, tablets, and capsules, in development and pilot plant laboratories, independently or with internal scientists.
- Characterize drug substances, excipients, drug product intermediates, and final solid dosage formulations to assess material attributes and formulation performance.
- Evaluate characteristics including powder flow, bulk and tapped density, particle size distribution, powder compaction properties, tablet hardness and tensile strength, solid fraction, friability, disintegration time, and solubility.
- Review and analyze experimental data, identify trends and takeaways, and propose hypothesis-driven follow-up experiments.
- Document research work in an electronic lab notebook in accordance with departmental documentation guidelines.
- Comply with EHS and safety requirements and complete required training.
- Present research findings and technical recommendations to cross-functional teams in the Synthetic Molecule Pharmaceutics group.
Benefits
- Choice of national medical and dental plans and a national vision plan, including health incentive programs.
- Employee assistance and family support programs, including commuter benefits and tuition reimbursement.
- At least 120 hours of paid time off and 10 paid holidays annually.
- Paid parental leave: 3 weeks for bonding and 8 weeks for caregiver leave.
- Accident and life insurance, and short- and long-term disability in accordance with company policy.
- Competitive 401(k) U.S. retirement savings plan.
- Employees’ Stock Purchase Plan offering eligible colleagues the opportunity to purchase company stock at a discount.
- May be eligible for a variable annual bonus based on company, team, and/or individual performance.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
