C

Catalent

Global contract drug formulation, manufacturing, packaging

Pharmaceutical Manufacturing Operator 1

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeKansas City, MO, USA

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 the ability to apply them effectively, is required.
  • The ability to manage priorities and projects effectively and work in a matrix organization is required.
  • The employee must maintain current knowledge of cGMP regulations and regulatory trends relevant to the responsibilities.
  • The employee must be able to sit, stand, and walk regularly and occasionally lift up to 40 pounds.
  • The employee must be able to wear a powered air-purifying respirator (PAPR) when required, wear required gowning in GMP manufacturing areas, and wear steel-toed safety shoes for 8 to 12 hours depending on shift duration.
  • The employee must operate safely in a dynamic environment with mobile and fixed equipment and changing conditions while completing simple to complex tasks and multitasking.
  • The employee must follow safety procedures and use personal protective equipment (PPE).

Responsibilities

  • Ensure cGMP compliance and maintain general good housekeeping.
  • Inform the Senior Pharmaceutical Technician or Pharmaceutical Manufacturing Lead when work orders are needed for processing rooms and equipment within the core group.
  • Meet and maintain 5S standards, keep the facility tour-ready, and maintain people, material, flow, cleaning, and zone concepts.
  • Learn batch records to ensure clarity and processing accuracy; keep training current and progressing for core group requirements under direction from the Senior Pharmaceutical Technician or Pharmaceutical Manufacturing Lead.
  • Ensure assigned operational areas process under GMP conditions and follow applicable standard operating procedures (SOPs).
  • Provide information to support core group metrics and efficiency increases.
  • Build proficiency with business-critical equipment within the core group while maintaining high quality standards.
  • Identify and communicate necessary adjustments to address potential safety concerns.
  • Perform other duties as assigned.

Desired Qualifications

  • Experience in a pharmaceutical or cGMP manufacturing environment, with 0–3 years preferred.
  • Knowledge of solid dosage manufacturing.

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

Recently Posted Jobs

Explore more opportunities at Catalent

See more jobs