We are currently hiring a QC pharma Projects Supervisor for a fixed-term period of 12 months at our Westport site. The QC Pharma Projects Supervisor will lead a team of 8-12 direct staff members within the Projects team. The role is responsible for overseeing the QC Pharma Projects team in supporting Operations cleaning validations, residual monitoring and method transfers to the QC laboratory.

Responsibilities

• Provide guidance to direct reports to ensure activities are completed on schedule, in a GMP-compliant manner and in line with regulatory, Quality Assurance, Environmental Health and Safety, and corporate requirements.
• Maintain strong relationships with management, colleagues, direct reports and customers across the business units and Quality function, and communicate analytical requirements clearly, concisely and professionally.
• Motivate the team and take appropriate corrective action on individual or team performance where required.
• Hold performance meetings in accordance with company policy.
• Update the time management system and take appropriate action where attendance or timekeeping is below the expected standard.
• Actively participate in the training and certification of new employees.
• Ensure the area is fully staffed and manage any constraints appropriately.
• Coach and develop team members to support company succession planning.
• Represent the company as a subject matter expert during regulatory inspections, as required.
• Provide analytical support and scheduling for residual monitoring, process validations and cleaning validations across all business units.
• Lead New Product Introductions from an analytical perspective, including method co-validation and onboarding of new hires.