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Cork, CO, T23, IE
Job details
Work flexibility: Hybrid
Req ID: R537480
Employee type:
- Temporary
- Full Time
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Why join Stryker?
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.
Job description
23 months fixed term contract
Stryker is one of the world’s leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives. We are currently seeking a Post Market Surveillance Analyst to join our Neurovascular Division to be based in Neurohub, Cork, Ireland.
Who we want
Detail-oriented process improvers. Critical thinkers who naturally see opportunities to develop and optimize work processes – finding ways to simplify, standardize and automate.
Meticulous documenters. Detail-oriented people who enjoy maintaining meticulous documentation of reports, metrics, proposals, and presentations.
Strategic thinkers. People who enjoy analyzing data or trends for the purposes of planning, forecasting, advising, budgeting, reporting, or sales opportunities.
Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
What you will do
As a Post Market Surveillance Analyst, you will enter customer complaints into the company-wide complaint system and follows methods to analyze the complaints for the Neurovascular business.
Responsibilities may include but are not limited to:
Review and determine reportability of complaints to FDA and international regulatory authorities.
Write, review, and file Medical Device Reports (MDRs) and international Vigilance Reports.
Works closely with Sales Representatives and health care professionals to obtain additional information.
Monitor quality, completeness and timeliness of complaint investigations.
Write customer response letters.
Contribute to achieving team performance metrics and goals.
What you needA Bachelor’s Degree in a technical or scientific discipline required.
0-2 years’ work experience
Strong written/verbal communication skills.
Proficient in Microsoft Office Suite, including Word, Excel and PowerPoint.
Excellent organizational, problem-solving, and analytical and time management skills.
Demonstrated problem-solving and troubleshooting skills.