Join Apotex as a Quality Oversight Manager to spearhead external quality operations for pharmaceutical products. Your work will ensure the highest standards are met across manufacturing partners.

In this pivotal role, you will manage quality oversight of all third-party finished products for Apotex, actively collaborating with both internal teams and external partners. You will be responsible for implementing and maintaining compliance with cGMP regulations, while fostering strong working relationships. Your leadership will impact product quality and compliance strategies effectively.

Key Responsibilities:
• Oversee quality issues for third-party manufacturing
• Engage in new product introductions to ensure quality
• Develop and review quality agreements with partners
• Drive improvement plans post-audit and inspections
• Assess customer complaints and initiate CAPA processes

Requirements:
• Bachelor's degree in relevant science field
• At least 10 years in QA/QC in the pharmaceutical sector
• Excellent grasp of manufacturing regulations
• Proven ability to manage multiple projects
• Preferred experience in sterile product manufacturing

Elevate quality assurance practices at Apotex and make a difference in global health standards.
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Quality Oversight Manager in Pharma