About the Company
Takeda Pharmaceuticals is a global, values-based, R&D-driven biopharmaceutical leader committed to bringing better health and a brighter future to patients by translating science into life-changing medicines. With a strong presence in the U.S., Takeda focuses its research and development efforts on four therapeutic areas: Oncology, Gastroenterology (GI), Rare Diseases, and Neuroscience. Our mission is powered by our people, who are dedicated to improving the lives of patients worldwide.
Job Description
We are seeking a highly skilled and motivated Formulations Scientist to join our dynamic R&D team in Rancho Cucamonga, CA. The successful candidate will play a critical role in the development of innovative tablet and liquid medicine formulations from pre-formulation to commercialization. This position requires a strong understanding of pharmaceutical sciences, formulation technologies, and regulatory requirements. You will be responsible for designing, executing, and interpreting experimental studies to advance our product pipeline.
Key Responsibilities
- Design and execute formulation development studies for solid oral dosage forms (tablets) and liquid formulations, including solutions, suspensions, and emulsions.
- Conduct pre-formulation studies to characterize drug substances and excipients, identifying potential formulation challenges.
- Develop and optimize manufacturing processes for various dosage forms at laboratory and pilot scales.
- Perform analytical testing of formulations using techniques such as HPLC, dissolution, particle size analysis, and rheology.
- Interpret experimental data, document findings in lab notebooks and technical reports, and present results to cross-functional teams.
- Collaborate with analytical, process development, and manufacturing teams to ensure successful product transfer and scale-up.
- Troubleshoot formulation and process-related issues, proposing effective solutions.
- Stay current with industry trends, regulatory guidelines (FDA, ICH), and new technologies in pharmaceutical formulation.
- Ensure all work is conducted in compliance with cGMP, safety, and quality standards.
Required Skills
- Bachelor's or Master's degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related scientific discipline.
- Minimum of 3 years of experience in pharmaceutical formulation development, specifically with tablets and liquid dosage forms.
- Proficiency in various formulation techniques and unit operations (e.g., blending, granulation, compression, coating, sterile filtration).
- Strong understanding of physicochemical properties of drug substances and excipients.
- Experience with analytical techniques used for formulation characterization (e.g., HPLC, dissolution, DSC, TGA).
- Excellent problem-solving, analytical, and communication skills.
- Ability to work independently and as part of a collaborative team.
Preferred Qualifications
- Ph.D. in Pharmaceutical Sciences or related field.
- Experience with QbD (Quality by Design) principles in formulation development.
- Familiarity with statistical design of experiments (DoE) software.
- Knowledge of biopharmaceutical classification system (BCS) and its implications for formulation.
- Prior experience in a GMP environment.
Perks & Benefits
- Comprehensive medical, dental, and vision insurance.
- 401k retirement plan with company match.
- Paid time off and company holidays.
- Employee assistance program.
- Professional development and training opportunities.
- On-site fitness center and wellness programs.
- Life and disability insurance.
- Employee stock purchase plan.
How to Apply
If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:
- An up-to-date Resume or CV
- A brief cover letter summarizing your experience and motivation
Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.
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