Pharmaceutical Development Scientist II – Formulation & GMP

Catalent; Kansas City (MO); On-site; USD 90,000 - 110,000; Full time

Job summary

Catalent's Kansas City facility is seeking a Pharmaceutical Development Senior Associate Scientist II to support formulation and process design for oral solid dosage forms and participate in clinical trial manufacturing. The role requires GMP compliance and meticulous documentation.

This onsite, full-time position in Kansas City, MO offers growth within a dynamic team. Shift is M-F 8am-5pm, and you will work with advanced technologies while collaborating with skilled professionals to deliver

Qualifications

• Bachelor's degree in life/physical science with 4+ years experience, or Master's with 2+ years.

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 expertise to complete assignments within the group or project team.
• Conduct work in GMP areas under minimal supervision.
• Perform other duties as assigned.

Education

Bachelor’s degree in a related life science or physical science field

Master’s degree in a related life science or physical science field

Job description

Catalent's Kansas City facility is seeking a Pharmaceutical Development Senior Associate Scientist II to support formulation and process design for oral solid dosage forms and participate in clinical trial manufacturing. The role requires GMP compliance and meticulous documentation.

This onsite, full-time position in Kansas City, MO offers growth within a dynamic team. Shift is M-F 8am-5pm, and you will work with advanced technologies while collaborating with skilled professionals to deliver