Formulation & Process Scientist I – Onsite

Catalent Pharma Solutions

Kansas City (MO)

On-site

USD 85,000 - 110,000

Full time

6 days ago
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Benefits offered by this job

Competitive PTO + 8 holidays
Benefits from day one (medical/dental/

Job summary

Catalent's Kansas City facility is seeking a Pharmaceutical Development Scientist I to support formulation and process design for oral solid dosage forms and participate in clinical trial manufacturing. The role requires strong communication, regulatory knowledge, and the ability to work under pressure to meet deadlines. Shift: M-F 8am-5pm.

Location: Kansas City, MO. 100% Onsite. You will develop lab plans, author documents, and mentor others while applying advanced pharmaceutics principles to

Qualifications

  • Bachelor's degree with 6+ years of related experience or higher degrees preferred.
  • Ability to proactively address work issues at team and individual levels.
  • Experience developing and executing procedures and manufacturing processes with quality.
  • Demonstrated ability to lead small team projects and identify unmet needs.

Responsibilities

  • Develop and execute laboratory work plans and schedules to meet milestones.
  • Author protocols, batch records, test methods, technical reports, and SOPs.
  • Train or mentor others on technical development or business issues.
  • Apply knowledge of high-shear granulation, fluid-bed tech, roller compaction, coating.
  • Execute efficiency improvement projects with moderate guidance.
  • Identify business opportunities on project basis and support design goals.

Skills

Formulation design
Process design
Communication skills
Team leadership
Troubleshooting

Education

Bachelors in life/physical sciences
Masters in life/physical sciences
PhD in life/physical sciences

Job description

Catalent's Kansas City facility is seeking a Pharmaceutical Development Scientist I to support formulation and process design for oral solid dosage forms and participate in clinical trial manufacturing. The role requires strong communication, regulatory knowledge, and the ability to work under pressure to meet deadlines. Shift: M-F 8am-5pm.

Location: Kansas City, MO. 100% Onsite. You will develop lab plans, author documents, and mentor others while applying advanced pharmaceutics principles to

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