Description
Are you looking for an amazing opportunity to join an award winning company in the medical device industry? With massive opportunity for career progression and the chance to enter a fantastic work environment, this could be the move that sets up 2016 to be your best year yet. Job Summary Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. This includes analysing quality trend data and taking appropriate action; supporting production on all quality related issues; investigating customer complaints; and ensuring an effective and robust quality system which complies with all relevant regulatory requirements. Principal Duties & Responsibilities*Formulates procedures, specifications, and standards for products and processes.
*Provides leadership for quality engineering projects from concept through design, implementation, testing, documentation, support, and maintenance.
*Develops and implements corrective/preventative action plans.
*Collects and analyzes data for gauge and product evaluation.
*Develop and maintain an effective and robust quality system which complies with all relevant regulatory requirements.
*Ensure all validation activity is effective and documented in a compliant manner.
*Complete in-depth investigations into customer complaints and implement corrective and preventative actions, as appropriate.
*Identifies critical personnel, gauges, procedures, and materials needed for the completion of new products.
*Ensures that suppliers have necessary information and facilities to deliver quality products.
*Certifies product builders to ensure they have the required skills to complete their operation. This is not an exhaustive list of duties or functions and may not necessarily comprise all of the "essential functions" for purposes of the ADA Requirements
*Third Level Degree in Quality or Engineering field
*1 Years service in ZOML (at start date)
*Excellent communication and influencing skills
*Microsoft Office Suite.
*Understanding of QSR/ISO regulations
*Risk assessment skills using FMEA methodology
*Product testing methods, and able to use hard gaging and optical comparators.
*Knowledge of statistics, process control, and process capability.
*Ability to work within a team environment and build relationships outside of the department as well as outside the company (suppliers, regulatory agencies, etc.).
*Facilitates team efforts on quality engineering projects.
*Ability to deliver, meet deadlines and have results orientation.
*Able to communicate both orally and in written form to multiple levels of the comp
*Demonstrated history of taking initiative, meeting commitments and assisting in the creation of new tools or solutions to achieve business results.
Are looking for a new challenge? A chance to join a thriving global company that continues to go from strength to strength? This is the role the role for you! Please apply below with an up to date CV.
No CV? Not Sure Yet? Give me call for more info and an opportunity to ask more questions Barry Smyth !