Quality & Compliance Lead

Found in: Talent IE C2 - 2 weeks ago


Dublin, Ireland CBRE Full time

CBRE Global Workplace Solutions is a leading global provider of integrated facilities and corporate real estate management. We are recruiting a Quality and Compliance Lead to join the team located in Dublin. The successful candidate will manage and monitor the day-to-day operations at various sites, determining compliance status of global regulatory standards and other pertinent regulatory requirements.

Role Summary:

Support the delivery and oversight of the quality compliance services at multiple client sites Execute quality compliance team activities that support the quality compliance contractual obligations Manage vendors, providing quality compliance support Interface with numerous account, corporate, and client functions Interface with site management to ensure quality compliance services are delivered to applicable regulatory and contractual requirements and to client satisfaction. Identify any quality, compliance, and / or contractual issues and communicate them to the appropriate customer management teams Work with teams to resolve any identified issues Support any quality investigations and Corrective Action / Preventative Action (CAPA) plans for work falling under the CBRE scope Ensure compliance with all regulations and license / certification requirements Maintain and submit all records and documents to the client and / or proper authorities Provide formal supervision to individual employees within single functional or operational area Approve subordinate's recommendations for staff recruitment, selection, promotion, advancement, corrective action and termination Plan and monitor appropriate staffing levels and utilisation of labour, including overtime Prepare and deliver performance appraisal for staff Mentor and coach team members to further develop competencies

Experience Required:

High school diploma or general education degree Bachelor's degree in science or engineering or equivalent related work experience (desirable) Strong experience in technical writing Knowledge of Quality Systems and Compliance within Life Science Environment(s) Supervisory experience PC Literate - Desktop publishing, Microsoft Office Suite and Online Help Knowledge of training records and records management Excellent interpersonal, writing, editing, analytical and organisational skills Review or audit of regulated documentation experience (desirable) Specialised training or certification in quality assurance audits, preferably FDA or ISO related (desirable)

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