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Catalent

Global contract drug formulation, manufacturing, packaging

Process Technician

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeStrathroy, ON, Canada$26.93 /hr

About the Job

Requirements

  • A high school diploma, GED/CAEC, and/or educational credential assessment is required.
  • The role requires being clean-shaven to wear a respirator, which is mandatory for health and safety.
  • The role requires frequent standing, walking, climbing ladders or steps, reading written documents, using a computer monitor, talking, and listening; occasional stooping, kneeling, crouching, bending, carrying, reaching with hands and arms, and occasional lifting and/or moving up to 25 kg; employees may be exposed to inclement weather or environments requiring protective gear and heightened safety awareness.
  • Candidates with non-Canadian credentials must provide an evaluation confirming Canadian equivalency as determined by the Alliance of Credential Evaluation Services of Canada, such as WES.

Responsibilities

  • Minimise equipment downtime and improve equipment availability by being accountable for delivering and reducing machine turnaround time.
  • Ensure the team consistently sets and upholds site safety best practices by demonstrating zero-tolerance behaviours, continually challenging and raising safety standards, eliminating risk to employees, products, and the environment through active participation in safety and accident investigations, and completing high-quality, current risk assessments.
  • Ensure the team consistently sets site quality best practices by demonstrating zero-defect behaviour and continually challenging and raising quality standards.
  • Ensure batch manufacturing records are accurately completed in real time to support timely documentation approval, follow processes and procedures including online and in-process quality checks rigorously to deliver consistent, high-quality products, and ensure all team members adhere to standard operating procedures and comply with individual current Good Manufacturing Practice responsibilities to prevent deficiencies.
  • Carry out specific targeted training as required and ensure ComplianceWire training requirements are completed within specified due dates.
  • Recommend improvements to the batch manufacturing process and standard operating procedures to increase process efficiency and effectiveness, and maintain 5S and continuous improvement activities.
  • Ensure all interactions and engagements are carried out with high ethical and professional standards and that all work is accomplished with quality and in accordance with Catalent values.
  • Perform other duties as assigned.

Desired Qualifications

  • At least two years of manufacturing-environment experience is preferred.
  • Good Manufacturing Practice work experience is preferred.
  • Pharmaceutical manufacturing experience is an advantage.
  • Good mathematics skills and ability to operate related computer applications.
  • Ability to work independently and complete daily activities.
  • Ability to write batch records.
  • Good standard of oral and written English and ability to follow written instructions.

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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