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Catalent

Global contract drug formulation, manufacturing, packaging

Pharmaceutical Manufacturing Operator 1

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeKansas City, MO, USANo salary listed

About the Job

Requirements

  • A high school diploma or GED is required.
  • Equipment process and framework knowledge, working knowledge of basic hand tools, and basic computer skills are required.
  • Knowledge of current good manufacturing practice (cGMP), Food and Drug Administration (FDA), Medicines and Healthcare products Regulatory Agency (MHRA), and Drug Enforcement Administration (DEA) guidelines and how to apply them effectively is required.
  • The candidate must be able to manage priorities and projects effectively and work in a matrix organization.
  • The candidate must maintain current knowledge of cGMP regulations and regulatory trends relevant to the responsibilities.
  • The candidate may be required to sit, stand, and walk regularly and occasionally lift up to 40 pounds.
  • The candidate must be able to wear a powered air-purifying respirator (PAPR) during manufacturing when required, wear required gowning in GMP manufacturing areas, and wear steel-toed safety shoes for 8 to 12 hours per shift.

Responsibilities

  • Ensure cGMP compliance and general good housekeeping, and inform the Senior Pharmaceutical Technician or Pharmaceutical Manufacturing Lead of work orders needed for processing rooms and equipment within the core group.
  • Ensure 5S standards are met and maintained, the facility remains tour-ready, and people, material, flow, cleaning, and zone concepts are maintained.
  • Build the ability to learn batch records to support clarity and processing accuracy; keep training current and progressing for core group requirements under the direction of the Senior Pharmaceutical Technician or Pharmaceutical Manufacturing Lead.
  • Ensure assigned operational areas process under GMP conditions and applicable standard operating procedures (SOPs) are followed.
  • Provide information to support core group metrics and efficiency improvements.
  • Build proficiency with business-critical equipment within the core group while maintaining high quality standards.
  • Follow Catalent safety procedures, identify and communicate necessary adjustments to address potential safety concerns, and ensure proper use of personal protective equipment (PPE).
  • Operate safely in a dynamic environment with mobile and fixed equipment and changing conditions while completing tasks ranging from simple to complex, including multitasking.
  • Perform other duties as assigned.

Desired Qualifications

  • Zero to three years of experience in a pharmaceutical or cGMP manufacturing environment is preferred.
  • Knowledge of solid dosage manufacturing is preferred.

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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