Onsite Pharma Development Associate II

Catalent, Inc.; Kansas City (MO); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Career growth opportunities

Diverse, inclusive culture

Paid time off

8 paid holidays

Tuition reimbursement

Job summary

Catalent is hiring a Pharmaceutical Development Associate Scientist II for our Kansas City, MO site. You will support formulation and process design for oral solid dosage forms, participate in clinical trial manufacturing, and ensure compliance with regulatory requirements and GMP.

This 100% onsite role involves executing lab work plans, drafting batch records and technical reports, training others, and contributing to efficiency improvements while maintaining high quality documentation and

Qualifications

• Bachelor's degree required in a life science or physical science field with 0+ years of experience.
• Basic knowledge of pharmaceutics principles and concepts.
• Ability to apply mathematical and scientific reasoning.
• Basic understanding of equipment/instrument operations and troubleshooting across multiple techniques.
• Excellent written and verbal communication with internal/external customers.
• Understanding of current Good Manufacturing Practices and ability to work in GMP environment under supervision.

Responsibilities

• Execute laboratory work plans and schedules with input from supervisors or senior team members.
• Draft batch records, technical reports and SOPs with guidance.
• Perform parallel review of manufacturing documentation and may qualify to perform technical review for accuracy and compliance.
• Train others on basic laboratory techniques.
• Assist in efficiency improvement projects with guidance.
• Maintain high-quality laboratory documentation per regulatory guidance and site procedures.
• Perform physical testing (bulk/tap density, FT4 flow analysis, sieve analysis).
• Execute procedures or methods of moderate complexity with high quality.

Skills

Pharmaceutics knowledge

Mathematical reasoning

Instrumentation troubleshooting

Communication skills

GMP understanding

Education

Bachelor's degree in Life or Physical Science

Job description

Catalent is hiring a Pharmaceutical Development Associate Scientist II for our Kansas City, MO site. You will support formulation and process design for oral solid dosage forms, participate in clinical trial manufacturing, and ensure compliance with regulatory requirements and GMP.

This 100% onsite role involves executing lab work plans, drafting batch records and technical reports, training others, and contributing to efficiency improvements while maintaining high quality documentation and