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Catalent

Global contract drug formulation, manufacturing, packaging

Quality Assurance Supervisor

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeStrathroy, ON, Canada$65k - $81k

About the Job

Requirements

  • A bachelor's degree in science, engineering (chemistry or biochemistry), or a related field is required.
  • At least 3 years of experience in quality assurance/quality control or a related field is required.
  • While performing the role, the employee must be able to talk and hear, sit, and use their hands and fingers to handle or feel and manipulate keyboard keys; manual dexterity is required. The employee must occasionally stand, walk, reach with arms and hands, bend or twist, and stoop, kneel, crouch, or crawl. Close vision is required, and exposure to chemicals is possible.
  • 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

  • Communicate daily work plans and priorities with the Quality team to meet product release timelines and expectations.
  • Collaborate with functional areas to resolve quality issues and ensure product compliance with cGMP, SOPs, and standards.
  • Lead, coordinate, and participate in investigations and corrective actions for deviations and documentation issues, ensuring timely closure.
  • Work with operations to support the quality management system and provide guidance on cGMP and SOP compliance during production and packaging.
  • Ensure manufacturing batch documents for finished products are properly maintained and controlled.
  • Review and approve quality documents, including Master Batch Production Records, specifications, directives, reports, and SOPs.
  • Liaise with customer QA contacts regarding quality issues and agreements.
  • Provide leadership, motivation, and training for employees, and monitor performance in line with company policies.
  • Perform other duties as required.

Desired Qualifications

  • At least 1 year of supervisory experience is preferred.
  • Experience working in manufacturing, pharmaceutical, and/or GMP facilities is preferred.
  • Understanding of overall business needs and objectives.
  • Expertise in tools to meet current and advancing cGMP requirements.
  • Strong verbal and written communication skills.
  • Ability to multitask and prioritize effectively.
  • Ability to respond quickly to a changing regulatory environment.
  • Candidates with non-Canadian credentials must provide an evaluation confirming Canadian equivalency as determined by the Alliance of Credential Evaluation Services of Canada (ACESC), such as WES.

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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