Senior Pharmaceutical Development Lead Scientist

Catalent

Kansas City (MO)

On-site

USD 140,000 - 190,000

Full time

14 days+
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Benefits offered by this job

Career growth
Diversity & inclusion
Paid time off & holidays
Medical benefits from day one
Tuition reimbursement

Job summary

Catalent is seeking a Pharmaceutical Development Lead Scientist I to spearhead formulation design and development of oral solid dosage forms at our Kansas City site. The role emphasizes regulatory compliance, GMP practices, and leadership of a multi-disciplinary team.

The candidate will design experiments, author technical documents, and drive client-facing project outcomes while mentoring junior staff in a fast-paced onsite environment in Kansas City, MO.

Qualifications

  • Bachelor's degree with 11+ years of related work experience preferred.
  • Expert in data interpretation and regulatory guidance.
  • Experience evaluating changes to controlled documents or project scope.
  • Strong written and verbal communication skills.
  • Leadership development and supervisory abilities are expected.

Responsibilities

  • Develop and execute lab work plans and schedules.
  • Author and approve technical documents such as protocols and reports.
  • Review documents for regulatory compliance and accuracy.
  • Train, coach and mentor team members.
  • Supervise technical staff and manage performance.
  • Act as technical lead on projects with customer interaction.
  • Identify opportunities and drive efficiency improvements.
  • Maintain high-quality laboratory documentation per regulatory guidance.

Skills

Leadership
Data interpretation
Regulatory knowledge
Communication skills
Project management
Mentoring

Education

Bachelor's degree in life/physical science
Master’s degree in related field
Doctorate in related field

Job description

Catalent is seeking a Pharmaceutical Development Lead Scientist I to spearhead formulation design and development of oral solid dosage forms at our Kansas City site. The role emphasizes regulatory compliance, GMP practices, and leadership of a multi-disciplinary team.

The candidate will design experiments, author technical documents, and drive client-facing project outcomes while mentoring junior staff in a fast-paced onsite environment in Kansas City, MO.

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