Equipment Process Engineer- Waterford

ICDS Recruitment

Waterford

Equipment ProcessEngineer- Waterford. You will supportt manufacturing systems. Technical expertise is required to maintain, develop, debug, and troubleshoot process and equipment issues. Outline of role responsibilities: Develop and implement process and equipment improvements with minimal impact to production operating under 24/7 environment. Identify and eliminate repetitious machine failures. Provide support to the Manufacturing, Maintenance, and Equipment Design groups. Utilise Lean Six Sigma tools along with data to drive continuous improvement. Objective to minimise scrap, increase yield, reduce turn-around-time, minimise manufacturing downtime and costs and ensuring quality manufacturing within given specifications. Develop methods to ensure personnel engaged in operationsmaintenance activities have sufficient knowledge to perform their assigned tasks. Prepare design specifications and associated documentation for equipment and system upgrades. Developing a detailed understanding of the process and automation systems in the manufacturing process, and sharing of technical expertise with colleagues. Fault-finding troubleshooting of equipment and process issues. Equipment installation and validations. Commissioning and Validation of automation lines. Implement improvements under change control. Develop methods to ensure personnel engaged in maintenance activities have sufficient knowledge to perform their assigned tasks. Generate documentation and SOPs associated with each of the equipment or process systems as required. Develop Functional and Detailed Design Specifications from formal and informal User Requirement Specifications. Be familiar with 21 CFR part 820 guidelines. Present, where appropriate, technical data to internal/external audit and inspection groups. Ensure Health and Safety Regulations and Procedure are adhered to at all times for self and others. Key cGMP Responsibilities : Follow Standard Operating Procedures at all times. Follow required applicable Regulatory standards as required. Ensure compliance to the QMS. Follow Personal Hygiene Rules as defined in the GMP Training Programme and notify area supervision of any health conditions which may affect the quality of product. Participate fully in all GMP and operational training programs and complete all Training Records in an accurate and timely manner. Desired Skills and Experience: Bachelors in Engineering (electronic/software) preferred. A minimum of 4 years in technical role in high volume manufacturing environment. Six sigma experience preferred. Solid Works experience preferred. Good problem solving abilities – able to identify facts, consider alternative approaches and evaluate the most appropriate action. Medical device and/or pharmaceutical industry experience preferred. Experience working in a validated environment with strong discipline with regard to change control is preferred. This job originally appeared on RecruitIreland.com.

2821 days ago