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Catalent

Global contract drug formulation, manufacturing, packaging

Operations Zone Manager

Machine & Process OperationConfirmed live in the last 24 hours
Full-timeKansas City, MO, USANo salary listed

About the Job

Requirements

  • A high school diploma or General Educational Development (GED) is required.
  • Ability to create and work within an operating plan framework and budget.
  • Thorough knowledge of equipment and processes used in pharmaceutical manufacturing.
  • Strong understanding of current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), Medicines and Healthcare products Regulatory Agency (MHRA), European Union (EU), and Drug Enforcement Administration (DEA) guidelines and their application.
  • Knowledge of solid dosage manufacturing.
  • Ability to manage priorities and projects effectively, with strong communication and people management skills.
  • Excellent computer skills.
  • Ability to work effectively in a matrix organization.
  • Demonstrable leadership experience at Catalent, including participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW, may be considered in place of external experience.

Responsibilities

  • Manage Pharmaceutical Manufacturing Technicians within the assigned zone, including selection, performance evaluation, counseling, and conflict resolution.
  • Collaborate with Supply Chain, Maintenance, and Quality Assurance to ensure efficient schedules and high-quality products.
  • Oversee daily performance against standards and schedules, resolving workflow and technical issues as needed.
  • Make personnel decisions regarding staffing, wages, and performance reviews while maintaining compliance with current Good Manufacturing Practices and safety regulations.
  • Ensure the facility remains tour ready and that people, materials, and cleaning processes are maintained effectively.
  • Execute training for Technicians on manufacturing and cleaning standard operating procedures and applicable regulations.
  • Oversee personnel allocation to ensure timely project completion and accurate batch records.
  • Provide updates to management and stakeholders on project timelines.
  • Troubleshoot processing, equipment, or utilities issues and support workforce motivation and training.
  • Define and implement Corrective/Preventive Actions in response to audits and deviations, driving process improvements through change control.
  • Support 24/7 operations as needed and perform other assigned duties.

Desired Qualifications

  • Five years of prior supervisory or relevant management experience, such as in pharmacy, chemistry, or science.

About the Company

Catalent

Global contract drug formulation, manufacturing, packaging

Catalent provides end-to-end contract development and manufacturing services for pharmaceutical, biotechnology, and consumer health products. Its offerings cover drug formulation, large-scale manufacturing, clinical supply, and packaging under long-term partnerships, coordinating through a connected supply chain to move products from development to market. It differentiates itself with a broad, integrated service platform and long-standing customer relationships that help clients accelerate development and ensure reliable supply. The company aims to help clients bring products to market efficiently while balancing quality, cost, and sustainability across the product lifecycle.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Franklin Township, NJ
Founded
1996

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