Laboratory Supervisor Central Services QC
- Westport, Co Mayo
- Permanent
- Full-time
- Lead and guide the Stability & Data Management Team to ensure timely and GMP-compliant completion of activities in line with regulatory and corporate standards.
- Develop and maintain strong relationships with management, colleagues, and customers across various business units and project teams.
- Oversee project management, including the creation of Gantt charts and managing projects from initiation through to successful completion.
- Motivate the team, addressing performance issues and conducting performance meetings as per company policy.
- Review and approve Stability Master Documents as required
- Manage team attendance and timekeeping, taking corrective action when necessary.
- Actively participate in the training and certification of new employees.
- Ensure adequate staffing within the area of responsibility, managing any constraints effectively.
- Coach and develop team members, supporting succession planning initiatives.
- Act as a subject matter expert during inspections, representing the company as required.
- Drive continuous improvement in the QC laboratories by identifying and implementing efficiencies and quality enhancements.
- Minimum of 3 years of experience in a QC environment within the pharmaceutical industry and proven project management experience.
- Supervisory experience or demonstrated attributes for effective people management.
- Scientific qualification in a relevant discipline with in-depth knowledge of laboratory GMP standards.
- Proficiency with electronic laboratory systems such as LIMS etc.
- Strong communication and conflict handling skills, with the ability to adapt to a dynamic environment.