Biologics Analytical Characterization Lead

Catalent Pharma Solutions

Kansas City (MO)

On-site

USD 90,000 - 140,000

Full time

14 days+
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Benefits offered by this job

Medical, dental, vision
Tuition reimbursement
Paid time off + 8 holidays
Career growth opportunities

Job summary

Catalent’s Kansas City facility is seeking a Group Leader, Analytical Characterization, Biologics to manage a sub-team of scientists and serve as a technical expert on projects. The role includes mentoring associates, supporting client audits, and coordinating analytical activities for Biopharma product development under cGMP guidelines.

Location: Kansas City, MO. Shift: Monday–Friday, 8:00 AM–4:30 PM. 100% onsite; opportunity to drive quality and growth within a dynamic team at Catalent.

Qualifications

  • Bachelor’s, Master’s, or Doctorate with relevant experience in department-specific techniques.
  • Leadership experience at Catalent or equivalent may substitute external experience.
  • Willingness to mentor and lead junior scientists and manage HR-related activities.

Responsibilities

  • Plan, prioritize, organize, and execute analytical work in the laboratory per client contracts.
  • Ensure cGMP practices are followed by the team and self.
  • Maintain safety and comply with SOPs and safety regulations.
  • Establish and maintain technical communications with other groups and clients as needed.
  • Conduct performance reviews and HR activities (time entry, PTO approvals, salary adjustments).
  • Foster team engagement and a learning culture.
  • Lead by example consistent with Catalent’s values and ethics.
  • Perform other duties as assigned.

Skills

Leadership
Project management
Coaching
Customer communication
Multitasking

Education

Bachelor's degree
Master's degree
Doctorate degree

Job description

Catalent’s Kansas City facility is seeking a Group Leader, Analytical Characterization, Biologics to manage a sub-team of scientists and serve as a technical expert on projects. The role includes mentoring associates, supporting client audits, and coordinating analytical activities for Biopharma product development under cGMP guidelines.

Location: Kansas City, MO. Shift: Monday–Friday, 8:00 AM–4:30 PM. 100% onsite; opportunity to drive quality and growth within a dynamic team at Catalent.

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