Pharma QA Specialist — Onsite & Impactful Role

Catalent Pharma Solutions; Canada; Remote; CAD 48,000 - 55,000; Full time

Benefits offered by this job

Health, Dental, Vision, Life Insurance

RPP Pension Plan

Development opportunities

Tuition reimbursement

Job summary

Catalent is seeking a Quality Assurance Associate for our Adair, Ontario facility. The role focuses on preventing quality issues, ensuring regulatory compliance, and supporting continuous improvement in a fast-paced pharmaceutical manufacturing environment.

You will perform in-process audits, final release activities, and coaching on documentation practices, contributing to cGMP standards and overall product quality.

Qualifications

• Bachelor’s Degree in Science, Engineering (Chemistry, Biochemistry) or related field.

Responsibilities

• Perform in-process document auditing and product quality checks; ensure issues communicated to production and QA, including QA sign-off.
• Conduct final release auditing of batch documentation for cGMP and SOP compliance.
• Assist in investigating manufacturing issues and deviations; coach operators on cGMP practices.
• Perform weekly compliance audits in production and packaging; prepare QA reports.
• Act as QA representative on shift for decision-making and issue resolution; escalate as needed.
• Assist in writing/revising SOPs and in filing, archiving, and review of quality documents.
• Perform finished product blister inspection prior to batch release.

Skills

Analytical skills

Problem solving

Communication skills

Independent work

Coaching/leadership

Education

Bachelors in Science/Engineering (Chemistry, Biochemistry)

Job description

Catalent is seeking a Quality Assurance Associate for our Adair, Ontario facility. The role focuses on preventing quality issues, ensuring regulatory compliance, and supporting continuous improvement in a fast-paced pharmaceutical manufacturing environment.

You will perform in-process audits, final release activities, and coaching on documentation practices, contributing to cGMP standards and overall product quality.