Complaints and Vigilance Specialist – Praca Poznań Sady, Tarnowo Podgórne
Miejsce pracy: Wielkopolskie / Poznań, Sady – gmina Tarnowo Podgórne
LiNA Medical Polska Sp. z o.o. – producent urządzeń medycznych w obszarze ginekologii małoinwazyjnej poszukuje pracownika na stanowisko: Complaints and Vigilance Specialist
Status Oferty Pracy: Aktualna
Dział: QA
Rodzaj pracy: Pełen etat
Your responsibilities
Register and manage customer complaints in a timely and accurate manner.
Oversee the entire complaint-handling process—from registration, classification, root cause investigation, corrective action definition, IMDRF code assignment, final reporting, and financial corrections in the ERP system.
Report incidents to relevant regulatory authorities worldwide.
Continuously monitor and analyze market requirements related to trend reporting and regulatory expectations.
Update internal procedures and reporting processes in response to regulatory changes.
Monitor key complaint management indicators and prepare statistical reports.
Supervise trend reporting processes to identify recurring issues and potential risks.
Act as the primary contact for distributors and regulatory authorities regarding complaints and medical incidents.
Collaborate closely with engineering, production, and quality control teams to investigate complaint root causes.
Work with Product Managers and participate in regular status review meetings.
Lead the complaint management team—facilitate root cause analysis meetings and define corrective actions.
Participate in the Corrective and Preventive Actions (CAPA) process, including initiating CAPAs based on complaint trends.
Align complaint handling with risk management processes, ensuring risk mitigation measures are properly implemented. Trigger risk analysis updates when necessary.
Our requirements
University degree in Quality Management, Engineering, or a related
Strong quality mindset and attention to detail.
Familiarity with ISO 13485 standards.
Minimum 2 years of experience in the medical device industry.
Knowledge of Medical Device Regulation (MDR) and FDA requirements is a plus.
Experience with quality tools and methodologies (e.g., 5 Whys, Ishikawa Diagram, 8D Report).
Proficiency in MS Office (PowerPoint, Excel); Power BI is a plus.
English proficiency at B2 level or higher.
Assertiveness and a positive, solution-oriented approach.
Strong communication and problem-solving skills.
What we offer
Full-time job contract.
Opportunity to work in an international environment.
A number of benefits (private medical care, sports card, flexible working time, Home Office, co-financing for English language classes, fruit and snacks).
Great atmosphere in the office and interesting challenges.
Opportunity to grow with the organization and build a successful career path.