About the Company
Bayer is a global enterprise with core competencies in the Life Science fields of health care and nutrition. Our products and services are designed to benefit people and improve their quality of life. At Bayer, we’re committed to advancing medical innovation and sustainable solutions. Join a team dedicated to making a tangible difference in the world.
Job Description
We are seeking a highly skilled and motivated Formulations Scientist to join our dynamic R&D team in Kansas City, MO. In this critical role, you will be responsible for the design, development, and optimization of pharmaceutical formulations, with a primary focus on tablet and liquid medicine dosage forms. You will contribute to the entire product lifecycle, from pre-formulation studies through process development and scale-up, ensuring robust and stable formulations that meet regulatory requirements and patient needs. This position offers an exciting opportunity to innovate and contribute to life-changing medicines.
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 activities to characterize active pharmaceutical ingredients (APIs) and excipients.
- Develop and optimize manufacturing processes for experimental and clinical batches.
- Perform stability studies and interpret data to determine shelf-life and appropriate storage conditions.
- Prepare comprehensive technical reports, development summaries, and regulatory documentation (CMC sections).
- Collaborate cross-functionally with analytical, process engineering, manufacturing, and regulatory teams.
- Operate and maintain laboratory equipment, ensuring compliance with GMP/GLP standards.
- Troubleshoot formulation and process challenges, implementing effective solutions.
- Stay current with scientific literature, industry trends, and new technologies in pharmaceutical formulation.
- Mentor junior scientists and contribute to a collaborative team environment.
Required Skills
- PhD in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related field; or MS with 3+ years of relevant experience; or BS with 5+ years of relevant experience.
- Proven experience in pharmaceutical formulation development for both solid oral dosage forms (tablets) and liquid formulations.
- Strong understanding of physicochemical properties of APIs and excipients.
- Proficiency in experimental design (DOE) and statistical analysis.
- Familiarity with various drug delivery technologies and formulation strategies.
- Knowledge of GMP/GLP regulations and ICH guidelines.
- Excellent problem-solving, analytical, and communication skills.
- Ability to work independently and as part of a multidisciplinary team.
Preferred Qualifications
- Experience with scale-up and tech transfer activities.
- Prior experience working with sterile liquid formulations.
- Familiarity with Quality by Design (QbD) principles.
- Experience with controlled release technologies.
- Strong publication record or patent contributions.
Perks & Benefits
- Comprehensive health, dental, and vision insurance
- 401k matching program
- Generous paid time off and holidays
- Life and disability insurance
- Employee assistance program
- Tuition reimbursement
- On-site fitness center
- Professional development and growth opportunities
- Discounts on company products
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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