Impactful Senior Scientist, Pharmaceutical Development

Catalent Pharma Solutions

Kansas City (MO)

On-site

USD 60,000 - 90,000

Full time

14 days+
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Benefits offered by this job

PTO + 8 paid holidays
401K match
Medical, dental and vision benefits

Job summary

Catalent is seeking a Pharmaceutical Development Senior Associate Scientist I for 2nd shift on-site in Kansas City. You will support formulation design and development of oral solid drug products and train others in clinical trial manufacturing operations according to cGMP/SOPs.

Maintain quality lab docs, draft notebooks, protocols and batch records. Lead small team projects and contribute to regulatory-compliant procedures, ensuring high-quality manufacturing processes.

Qualifications

  • Bachelor’s degree in a life or physical science with at least 2 years of related experience, or a Master’s degree.
  • Ability to interpret written, oral, diagram, or schedule instructions.
  • Physical requirements include standing, walking, and lifting up to 50 pounds, with respirator use when required.

Responsibilities

  • Maintain high quality laboratory documentation in accordance with regulatory guidance and Site SOPs.
  • Draft technical documents such as laboratory notebook writeups, protocols and batch records.
  • Trains others on procedures and laboratory techniques.
  • Executes efficiency improvement project with guidance.
  • Has applied knowledge of the principles and concepts of a discipline.
  • Applies technical and functional knowledge to job related duties on most projects/ assignments within own group/project team.
  • Performs parallel review of GMP documents and laboratory notebooks and may become qualified to conduct compliance technical reviews.
  • Develop and executes procedures, methods, manufacturing processes with minimal complexity, with high quality.
  • Demonstrated ability to lead small team projects.
  • All other duties as assigned.

Skills

Laboratory documentation
Technical writing
Training others
Project coordination

Education

Bachelor’s degree in life sciences or physical sciences

Job description

Catalent is seeking a Pharmaceutical Development Senior Associate Scientist I for 2nd shift on-site in Kansas City. You will support formulation design and development of oral solid drug products and train others in clinical trial manufacturing operations according to cGMP/SOPs.

Maintain quality lab docs, draft notebooks, protocols and batch records. Lead small team projects and contribute to regulatory-compliant procedures, ensuring high-quality manufacturing processes.

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