Clinical Analyst

Il y a 6 mois


Gent, Belgique Agfa Temps plein

Agfa HealthCare, is a division of the Agfa-Gevaert Group which is headquartered in Mortsel, Belgium and traded on Euronext Brussels (AGFB). At Agfa HealthCare, we support healthcare professionals across the globe to transform the delivery of care. Our focus is 100% on providing best-of-suite Imaging IT software solutions that enable secure, effective and sustainable imaging data management. From product development to implementation, our unified Enterprise Imaging Platform is purpose-built to reduce complexity, improve productivity and deliver clinical value. We use our proven track record as an innovator, our in-depth medical knowledge and our strategic guidance to help healthcare providers achieve their clinical, operational and business strategies.

The main focus of this role is to assess clinical safety risk for complaints and problems in case of failures in the delivery of our IT products and services to our customer install base. The individual will focus on potential and actual risk analysis with the support teams or problem analysts and appropriate customer contacts for clinical evaluation. The Clinical Analyst decides if a Health Hazard Evaluation (HHE) is required and will own and drive the risk assessment.
The Clinical Analyst works closely with the Product Quality Manager and is part of the respective Product Quality Team (PQT) to provide clinical input to that team for specific Problem Records. The incumbent must possess strong clinical domain experience in Radiology and / or Cardiology.

**Main Responsibilities**:

- Review and assess complaints flagged for actual or potential harm for incident reportability according to the regulations and decide if a full Risk Assessment (HHE) is required
- Create Problem Records for these situations and own the clinical analysis. Provide input into problem record to accurately determine severity of problem.
- Complete the Health Hazard Evaluation (HHE) as part of the risk assessment.
- Clinical Analysts are available to all levels of support for consultancy on potential patient safety complaints
- Provide clinical input into any Medical Device Recalls, or Correction and Removal plans as it relates to the Health Hazard Evaluation.
- Provide input into IITS Problem Management process being a member of the Product Quality Team (PQT)
- Maintain working knowledge of current products and solutions.

**Competencies (skills, knowledge, behaviors)**:
**Education, Experience and Skill Requirements**:

- Degree or Diploma in a Cardiology or Radiology technical field or an equivalent combination of education and experience
- Degree or Diploma in a technological field or an equivalent combination of education and experience
- 3 or more years previous work experience in a clinical customer environment
- Excellent computer skills including MS 365
- Excellent oral, written and interpersonal communications skills
- Proven organizational and time management skills
- Demonstrated experience adapting to change
- Strong customer orientation, interacting with both internal and external customers
- Previous experience working in a global environment (networking and building relationships with individuals in remote locations)
- Strong understanding of the regulated medical device environment.
- Cooperation & Teamwork.
- Precise and accurate
- Quality and compliance minded

**Other**:

- This description is not intended to be an exhaustive list of responsibilities for this position.
- As such, additional activities & skills not listed here may be involved, and other duties as assigned by management may be required of the incumbent

We offer a rewarding career in a field that impacts lives, the opportunity to work with a talented and committed team of individuals, training and career development programs, and a competitive compensation and benefits package. If you want to be part of this experience, we'll take you there

Learn more about Agfa HealthCare and follow us Instagram.


  • Qc Analyst

    Il y a 5 mois


    Gent, Belgique Eurofins Belgium BioPharma Services Temps plein

    **Company Description** Eurofins CDMO is a leading international Contract Development and Manufacturing Organization (CDMO) based in Europe. Our company focuses on drug product development and manufacturing for chemical/biological entities and drug substance development and manufacturing for biological entities. We support small and major biopharmaceutical...

  • Qc Analyst

    Il y a 5 mois


    Gent, Belgique Eurofins Belgium BioPharma Services Temps plein

    **Company Description** Eurofins CDMO is a leading international Contract Development and Manufacturing Organization (CDMO) based in Europe. Our company focuses on drug product development and manufacturing for chemical/biological entities and drug substance development and manufacturing for biological entities. We support small and major biopharmaceutical...


  • Gent, Belgique Cerba Research Nederland Temps plein

    **Who we are** We are Cerba Research and we provide the highest quality specialized laboratory and diagnostic solutions while leveraging patient data and scientific insight to shape and advance clinical trials. With our global footprint and access to leading regional labs, data, patients, technology, and partnered resources, we support global biotech,...

  • Product Manager

    Il y a 3 mois


    Gent, Belgique Clinisys Temps plein

    Clinisys is a global provider of intelligent diagnostic informatics solutions and expertise designed to redefine the modern laboratory, across healthcare, life sciences, and public health. Millions of diagnostic results and data insights are generated every day using Clinisys’ platform and cloud-based solutions in over 3,000 laboratories across 34...


  • Gent, Belgique Ardena Temps plein

    **About us** **Ardena **is a leading contract development organization for the pharmaceutical industry. We assist pharmaceutical companies, from virtual biotech to big pharma, in bringing their valued molecule(s) to the clinic and market. We provide a comprehensive and integrated portfolio of drug substance and drug product development, manufacturing,...


  • Gent, Belgique Legend Biotech EU Temps plein

    **Company Information** Legend Biotech entered into a global collaboration agreement with Janssen Biotech, Inc. to develop, manufacture and commercialize ciltacabtagene autoleucel (cilta-cel). Through our strategic partnership, we look to advance the promise of an immunotherapy in the treatment of multiple myeloma. **Role Overview** The QC Investigation...


  • Gent, Belgique Clinisys Temps plein

    Clinisys is a global provider of intelligent diagnostic informatics solutions and expertise designed to redefine the modern laboratory, across healthcare, life sciences, and public health. Millions of diagnostic results and data insights are generated every day using Clinisys’ platform and cloud-based solutions in over 4,000 laboratories across 39...

  • Qc Support Technician

    Il y a 5 mois


    Gent, Belgique Legend Biotech EU Young Graduates Temps plein

    As a Quality Control Support Technician at Legend Biotech, you're stepping into a role that's more than just a job. It is your chance to make an impact on patients' lives worldwide. Being part of our Quality Operations Team, you will work closely with team leads and QC analysts to clean and disinfect materials, and to ensure a seamless transfer of samples...