Quality Supervisor -Incoming Inspection

CPL

Galway

Quality Supervisor –Incoming Inspection. The Quality Supervisor is responsible for managing the Quality Control Inspection team. Job Responsibilities: Provide Direct Supervision to Quality Inspectors ensuring that all resources are properly trained and cross trained as required across Incoming, In Process and Final Inspection steps. Manage daily work assignments of Quality Inspectors including overseeing employee job performance such as attendance, quality and productivity. Plan, assigns and adjusts work priorities to meet daily, weekly, monthly customer sales order requirements. Supports Quality reporting metrics; provides data for tracking metrics. Assists in development of root-cause analysis and ensures corrective/ preventive actions are implemented to address non-conformances. Initiation and support of continual improvement solutions for new and enhanced methods for inspection, testing, and evaluation of data throughout the companies processes. Work with relevant Engineering Teams to establish inspection plans, frequencies and test methods for incoming material/parts. Overall responsibility for GMP standards and compliance within the manufacturing area, key lead in external Regulatory and Customer audits for inspection areas. Manage assigned aspects of the quality system in compliance with ISO 13485, FDA QSR, MHLW and Canadian Quality System requirements. Quality system training of our client’s personnel as per defined training plans. Perform other assigned tasks and support all aspects of the Quality System as directed by the Manager. Job Requirements: BE/BS Degree. A Post-graduate qualification in Quality Assurance is preferable although not mandatory. At least three to five years Quality Supervisor experience in an inspection/lab environment or related role within the medical device industry. Ability to work on own initiative and lead a team. Strong team member with the ability to identify and drive implementation of innovative quality improvements. Ability to consistently meet deadlines. Demonstrate and actively promote high levels of professional Supervisory skills. Good communication skills. Must have the ability to communicate effectively at all levels of the company. Ability to write clear, concise technical reports. Good administrative/organizational ability with high level of attention to detail. Ability to liaise with suppliers, customers and regulatory contacts in an informed professional manner. Thorough understanding of ISO 13485 and FDA QSR. For more information contact Fiona Rattigan on 091 507 515 or email an updated CV to Fiona.rattigan@cpl.ie. Visit www.cpljobs.ie for more Engineering roles. This job originally appeared on RecruitIreland.com.

1837 days ago