Werfen is a growing, family-owned, innovative company founded in **** in Barcelona, Spain.
We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant.
Through our Immunoassay business line, we research, develop, and manufacture customized assays and biomaterials.
We operate directly in 30 countries, and in more than 100 territories through distributors.
Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.
Within a medical device environment, work with the QARA Manager to ensure regulatory compliance and certification of software products.
Key Accountabilities Be a key part of a team where you will: Collaborate in maintaining the quality system documentation processes and procedures adopted by the company.
Investigate and resolve quality issues, implementing corrective and preventive actions to mitigate recurrence.
Coordinate and support the preparation of software technical documents appropriate for regulatory submissions.
Support the regulatory submissions for market authorization for medical device products.
Conduct internal assessments and audits to identify areas for improvement and ensure adherence to established procedures.
Facilitate the approval process for software releases.
Disseminating knowledge about the Quality System and regulatory requirements.
Review Promotional and advertising materials.
Oversee post-market surveillance activities related to medical device products.
Offer guidance and mentorship to QARA team members at lower levels Networking/Key relationships The main relationships within to the Werfen Group are: QARA Manger, QA Leads, Validation Led Factory Lead and Solution Leaders Customer Application Lifecycle manager (ALM) Notified Bodies and Competent Authorities for product regulatory compliance.
This position may also require also cooperating with other companies inside Werfen.
Minimum Knowledge & Experience required for the position: Engineer, computer Science or other Technical carrier, or equivalent work experience.
A minimum of 5 years experience in Quality Assurance or Regulatory related, preferably within the Healthcare sector Additional Skills/Knowledge: Knowledge and experience working with medical device international regulations and related standards (ISO *****, ISO *****,..).
Knowledge and experience working in Medical device software life cycle process (IEC *****) Desirable: Knowledge and experience working in medical device regulatory submissions (MDR/IVDR,FDA..) Internal auditor qualification for management systems or knowledge of auditing techniques Skills & Capabilities: The adecuado candidate for this position will exhibit the following skills and competencies: Good level of Technical and Conversional English.
Team player with ability to work independently.
Excellent and effective written and verbal communication skills.
Excellent interpersonal skills, good judgment and analytical skills.
Effective time management and organizational skills What we offer: A meaningful project that will impact the quality of laboratory software medicine worldwide 3 days a week working from home Multicultural and friendly team Exciting opportunities for professional development.
Ongoing training Social benefits: Canteen, nursery check, English training...
All the benefits according to the chemical agreement Our Purpose: We contribute to the advancement of patient care around the world through innovative specialized diagnostics JOIN US!