Description
Quality Engineer/Limerick/11 Months Contract/Up to 34 EUR (Per Hour)
Provides leadership and support to Water Room and Formulations process, and ensures good Quality Engineering practices are in use. Drives continuous improvement through data driven approaches and monitoring of quality systems.
Job Responsibilities
* Provides complex product team support for quality system design and audit, compliance assessment, and for support of steady state manufacturing processes
Utilizes multifaceted industry and process excellence standards on an expert level in daily quality operations, including good manufacturing practices (GMP), equipment engineering system (EES), and international organization for standardization (ISO).
* Addresses and corrects product and process complaints.
Ensures comprehensive measurement systems to monitor effectiveness of quality and reliability systems to identify, bracket, correct and prevent defects, presenting reports to management
Responsible for supporting the activities of operations/Engineering/information management in building quality into our products and assuring compliance to the pertinent regulations while at the same time attaining operational effectiveness
Leads and executes upgrades to Quality System
Support QA programs in assuring compliance to the pertinent regulation
Identify and lead cost and technical improvements under the departments' continuous improvement program.
* Provide key inputs and leadership into transformational process developments.
* Project Management - provide timely and accurate reporting on project activities.
* New Product Introductions & Product Transfers
Lead or actively participate in cross-functional teams to ensure New Product Introduction/Research and Development projects are completed in a timely and efficient manner.
* Actively interfacing with cross-functional team members, always practicing good team work in support of day to day operating requirements.
* Demonstrate strong leadership and a clear identifiable work ethos within the team.
* Develop and maintain a Credo & Behavioural Standards based culture within the group.
* Ensure effective closure on Quality System documents (Audit Actions, NCR's, CAPA's, Maps, etc).
* Ensure all process developments, NPI etc are managed in accordance with the Quality management system.
* Implementation of safety/environmental requirements on purchase of all new equipment.
* Work with team leader to develop and implement strategic engineering Goals & Objectives.
* Support the implementation of all engineering and plant strategic initiatives.
Ensuring continuous improvement and understanding of measurement systems used on-site, driving down variance in test methodology.
* Develops site knowledge on manufacturing process knowledge, and monitors inputs and outputs to the processes, and implements and drives corrective actions.
Non Technical Skills and Additional Details
Education and Experience Required for Role:
* Degree qualified with relevant experience in Medical Devices/Pharmaceutical Industry
* Ability to work on own initiative Flexible work ethic Attention to detail CAPA and RCI experience. Excellent IT skill eg, experience in minitab, excel reports
* Risk management experience
* Automated process controls experience
* Good presentation skills
Responsibilities and accountabilities will vary for all positions and the scope of individual roles may not be limited to the contents of this position description.
Johnson & Johnson is an American multinational medical devices, pharmaceutical and consumer packaged goods manufacturer founded in 1886.
If you match these requirements, please apply in the normal way. Elevate will send you an email, please open, click and action that email and your application will be visible to the hiring organisation directly.