Working at Freudenberg: "We will wow your world!" This is our promise. As a global technology group, we not only make the world cleaner, healthier and more comfortable, but also offer our 52,000 employees a networked and diverse environment where everyone can thrive individually. Be surprised and experience your own wow moments.
At Freudenberg Medical, we make products that save and improve the lives of people every day, all around the world. We are a global provider for medical device design and manufacturing with more than 2,500 employees. Innovation is at the core of our company, and we are proud of our industry-leading quality, lean manufacturing, and focus on innovation in products and processing technologies. Freudenberg Medical is an exciting place to work with lots of opportunity to learn, develop, and grow your career. Come join us and together we can make a difference in the future of healthcare.
Some of your Benefits
Company Pension: Save for retirement with the company's help.
Health Insurance: Rely on comprehensive services whenever you need it.
Health Management: We support you to stay and become healthy and fit.
Education Reimbursement: Receive financial aid to help propel your career to the next level.
Cafeteria/ Canteen: We offer fresh food on-site, both hot and cold.
Carrick-on-Shannon (Co. Leitrim)
On-Site
VistaMed Ltd.
You support our team as
QA Engineer (Validation)
Responsibilities
* This involves but is not limited to:
* Ensuring that product introductions & change controls are effectively managed in accordance with the requirements of ISO 13485, MDD 93/42/EEC & MDR 2017/745.
* Participation in the new product introductions programmes to ensure that they are effectively introduced in accordance with the requirements of ISO 13845. Generation of Product Technical Files & associated studies in accordance with MDD 93/42/EEC & MDR 2017/745 when appropriate.
* Completion of Validation Programme – Risk Analysis, VMP, IQ’s, OQ’s, PQ’s as required according to procedure QAP 030 and other related procedures.
* Management of QA/Technical/Associate/Engineers (Validation), as applicable (Senior QA Engineer (Validation)).
* Review and Release of batch paperwork for Product release.
* Adhere to Plant Safety requirements and Health & Safety requirements relating to your work, assuming responsibility for those aspects of the OH&S System over which you have control to ensure the health and safety of yourself and others.
* Be aware of the potential environmental impacts associated with your work and the implications of non-conformance.
* Contribute to enhanced energy performance by conservation of energy where possible (Lighting, Equipment, Air Conditioning etc).
Qualifications
* Degree in Engineering/Manufacturing/Quality with emphasis on Medical Devices/Biomedical.
* Ideally 2-3 years previous experience as Quality/Validation Engineer in Medical Device/Pharma Environment.
* An Associate position may exist where there is limited experience.
* A Senior position may exist for a minimum of 6 years’ experience.
The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law. #J-18808-Ljbffr