Quality Assurance Supervisor: cGMP Compliance Lead

Catalent Pharma Solutions

Strathroy-Caradoc

On-site

CAD 65,000 - 81,000

Full time

14 days+

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Benefits offered by this job

Health, dental, vision, and life保险
Group retirement savings with employer
Tuition reimbursement

Job summary

Catalent Pharma Solutions in Strathroy, Ontario, is seeking a Quality Assurance Supervisor to lead the QA team, ensure cGMP compliance, and manage batch release processes onsite. The role emphasizes quality systems support and continuous improvement initiatives within a 100% onsite setting.

The candidate should have a science/engineering background, 3+ years in QA/QC with supervisory experience, and strong documentation and leadership skills.

Qualifications

  • Bachelor’s degree in science, engineering or related field.
  • 3+ years QA/QC experience with at least 1 year supervisory.
  • Must be able to communicate clearly and document quality issues.
  • Familiarity with cGMP, SOPs and batch documentation.
  • Willingness to work onsite in Strathroy, Ontario.

Responsibilities

  • Communicate daily work plans and priorities with the Quality team to meet release timelines.
  • Collaborate with functional areas to resolve quality issues and ensure cGMP compliance.
  • Lead investigations and corrective actions for deviations and documentation issues.
  • Support the quality management system during production and packaging.
  • Ensure manufacturing batch documents are maintained and controlled.
  • Review and approve quality documents and directives.

Skills

Leadership
Communication
Quality systems
cGMP knowledge
Documentation
Problem solving

Education

Bachelor’s degree in science/engineering

Job description

Catalent Pharma Solutions in Strathroy, Ontario, is seeking a Quality Assurance Supervisor to lead the QA team, ensure cGMP compliance, and manage batch release processes onsite. The role emphasizes quality systems support and continuous improvement initiatives within a 100% onsite setting.

The candidate should have a science/engineering background, 3+ years in QA/QC with supervisory experience, and strong documentation and leadership skills.

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