Quality Validation Technician III - 18 month contract - Medtronic Athlone
Medtronic Athlone and Bigmeadow, County Westmeath, Ireland
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
A Day in The Life Of:
* As part of the Advanced Manufacturing Engineering projects team, prepare process validation protocols and work with the relevant process engineer or technician in terms of execution of the validation and documentation of the resulting test report.
* Working with the Engineering and supporting Operations teams to contribute to the development of robust processes for new products.
* Running validation Performance qualification orders, measuring samples, analyzing data, and compiling reports.
* Risk Management – As part of a team co-ordinate the completion of Risk Management to include the use of tools such as Failure Modes Effect Analysis (FMEA), Fault Tree Analysis etc. to all product groups.
* The role also involves helping to ensure our products are manufactured to comply with product design requirements and Quality compliance.
* Meeting with cross functional teams to help progress projects, giving insight into Quality and Compliance requirements and making recommendations.
* Suggest and implement relevant changes to procedures and update to standard operating procedures as necessary.
* Performs a variety of duties in the quality, engineering, process, and development areas.
* Can interpret schematics, engineering drawings, written and verbal instructions.
* Work with the relevant project engineers in resolving issues encountered.
* Trains and mentors others.
Key Skills & Experience:
* Minimum NFQ Level 6 in a technical discipline.
* Requires minimum of 4 years of relevant experience in a highly regulated environment, typically Medtech/Pharma/Plastics processing environments.
* A dynamic team player with a positive attitude that can work effectively on cross-functional teams.
* Experience in writing SOPs, Standard Work’s, and Reports is desirable.
* Ability to work independently with general supervision.
* Flexible and willingness to travel for equipment testing and training.
* A good communicator and fluent in English, both in written and spoken.
Physical Job Requirements:
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
About Medtronic:
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 90,000+ passionate people.
Seniority level:
Mid-Senior level
Employment type:
Contract
Job function:
Management and Manufacturing
Industries:
Medical Equipment Manufacturing, Hospitals and Health Care, and Pharmaceutical Manufacturing
#J-18808-Ljbffr