Pharmaceutical Development Scientist II: Formulations & GMP

Catalent Pharma Solutions; Kansas City (MO); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Medical, dental, and vision benefits —

Tuition reimbursement

8 paid holidays

Onsite position in Kansas City

Job summary

Catalent Kansas City is hiring a Pharmaceutical Development Scientist II to support formulation and process design for oral solid dosage forms and contribute to clinical trial manufacturing. The role emphasizes GMP compliance, cross-functional teamwork, and high-quality execution in a 100% onsite Kansas City, MO environment.

The candidate will train others, lead small projects, and apply core principles within the discipline, with strong communication and technical skills under pressure to

Qualifications

• Ability to proactively address work issues at both an individual and team level.
• Ability to propose deviations from established procedures and methods based on sound judgment.
• Experience developing and executing procedures, methods, and manufacturing processes with minimal complexity and high quality.
• Demonstrated ability to lead small team projects and identify unmet needs within the department.
• Basic to moderate understanding of manufacturing equipment operations and troubleshooting skills in multiple techniques.

Responsibilities

• Train others on procedures and laboratory techniques.
• Execute efficiency improvement projects with guidance.
• Apply knowledge of principles and concepts within the discipline.
• Use technical and functional knowledge to perform duties on most projects or assignments within the group or project team.
• Conduct work in a GMP area under minimal supervision.
• Perform all other duties as assigned.

Skills

Leadership

Problem solving

Communication

GMP experience

Project execution

Education

Master’s degree in life or physical science

Doctorate in life or physical science

Job description

Catalent Kansas City is hiring a Pharmaceutical Development Scientist II to support formulation and process design for oral solid dosage forms and contribute to clinical trial manufacturing. The role emphasizes GMP compliance, cross-functional teamwork, and high-quality execution in a 100% onsite Kansas City, MO environment.

The candidate will train others, lead small projects, and apply core principles within the discipline, with strong communication and technical skills under pressure to