Join Bora Pharmaceuticals as a QA Compliance Specialist, managing quality assurance processes in a full time, 18-month contract role. Your focus will be on GMP compliance across projects.

This position at Bora Pharmaceuticals requires a proactive QA Compliance Specialist to support diverse departments including Engineering and Production. Your key tasks will involve issuing critical quality documents and analyzing systems to maintain compliance amidst complex product transfers. Engage in supplier management and lead investigations to enhance product quality standards globally.

Key Responsibilities:



• Plan and manage global compliance requirements • Author and approve standard operating procedures • Identify process vulnerabilities and drive remediation • Conduct supplier reviews for compliance assurance • Participate in internal audits and training

Requirements: • Bachelor’s degree or College Diplomas in relevant fields • At least 5 years of quality experience in pharmaceuticals • In-depth knowledge of GMP standards • Skilled in risk management and quality metrics • Advanced proficiency with office and electronic systems

Leverage your QA expertise at Bora Pharmaceuticals to impact global drug quality. #J-18808-Ljbffr

📌 Lead QA Compliance for Pharmaceuticals (Winnipeg)
🏢 Bora Pharmaceutical Services
📍 Winnipeg