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     

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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.
  • Internal and external training.
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Skontaktuj się z nami

  • rekrutacja@lina-medical.com
  • (+48) 61 222 21 21
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