Lead a dynamic quality control team at AbbVie as a QC Pharma Projects Supervisor for 12 months. Oversee cleaning validations, method transfers, and ensure compliance with GMP standards.
At AbbVie, the QC Pharma Projects Supervisor will guide a team of 8-12 members, overseeing critical QC activities within the Westport site. This role requires strong leadership and analytical skills while maintaining relationships with various business units. The supervisor will ensure that operations adhere to regulatory requirements, focusing on timely completion of tasks and staff training.
Key Responsibilities:
• Guide team to meet GMP-compliant schedules
• Maintain effective communication across departments
• Motivate team performance and manage attendance




• Conduct performance meetings as per policies
• Provide analytical support for process validations
Requirements:
• Degree in a science discipline, preferred in chemistry
• 3+ years as an analyst in GMP environments
• Experience with HPLC and GC analytical techniques
• Robust conflict handling and analytical skills
• Proven ability to build collaborative relationships
Transform quality assurance processes while leading a dedicated team at AbbVie.
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📌 QC Pharma Projects Supervisor at AbbVie (Westport)
🏢 AbbVie
📍 Westport