FSP Associate Scientist: Pharmaceutics, Solid Dosage Preparation

Thermo Fisher Scientific • South San Francisco, CA

2d

About The Position

The Associate Scientist supports solid dosage formulation preparation and characterization within Thermo Fisher Scientific’s PPD Laboratory Services and Synthetic Molecule Pharmaceutics group. The role prepares formulations such as blends, tablets, and capsules in development and pilot plant laboratories; evaluates materials and formulation performance; analyzes experimental results; and communicates findings and recommendations to cross-functional teams. The position requires accurate documentation, adherence to departmental procedures, and compliance with environmental, health, and safety requirements.

Requirements

• Bachelor’s degree in chemistry, material sciences, pharmaceutical sciences, chemical engineering, or a closely related area.
• Comparable experience of 0 to 1 years; an equivalent combination of appropriate education, training, and directly related experience may be considered.
• Proficiency in following complex, repetitive experimental protocols and batch records without deviation.
• Demonstrated proficiency in Microsoft Office, including Excel, Word, and PowerPoint.
• Excellent organizational skills and the ability to maintain focus and quality during routine tasks while meeting deadlines under pressure.
• Clear written and verbal communication skills to accurately record data 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, including blends, tablets, and capsules, independently or with internal scientists in development and pilot plant laboratories.
• Characterize drug substances, excipients, drug product intermediates, and final solid dosage formulations.
• Evaluate 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 key findings, and propose hypothesis-driven follow-up experiments.
• Document research work in an electronic lab notebook and follow departmental documentation guidelines.
• Comply with environmental, health, and safety requirements and complete required training.
• Present research findings and technical recommendations to cross-functional teams within 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, including 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.
• 401(k) U.S. retirement savings plan and other retirement and savings programs.
• Employees’ Stock Purchase Plan, offering eligible colleagues the opportunity to purchase company stock at a discount.
• Potential eligibility for a variable annual bonus based on company, team, and/or individual performance results.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level