Temp Quality

hace 4 semanas

Cornellà de Llobregat, Barcelona, España ZimVie A tiempo completo

We are ZimVie , a publicly traded, global life sciences leader focused on restoring daily life by advancing clinical technology to improve patients' smiles, function, and confidence. Our company is founded on a legacy of trusted brands, products, and clinical evidence made possible through an inclusive and collaborative culture that empowers our team members to bring their whole selves – their best selves – to work every day to accomplish our Mission. Together, our dedicated, diverse global team is shaping an exciting future for ZimVie — we hope you'll consider being a part of it

About the role:

This role will be responsible for performing duties to maintain regulatory compliance for products marketed by ZimVie, with a primary emphasis on communications with Competent Authorities. Responsibilities include the preparation and maintenance of Technical Documentation and participation in production transfers and new product development.

What you'll be doing:

  • Registrations of products in EMEA area
  • Maintain and update Health Authorities databases for Medical Device placing in the market and commercialization, as well as international internal databases on registrations.
  • Provide requested documents to each subsidiary/distributor in the on a case-by-case basis and in accordance with National laws.
  • Participation on external audits by NBs and Inspections by CAs and performance of internal audits to subsidiaries and supplier's audits.
  • Respond to all market requests (customers, subs, distributors and others).
  • Support CS in providing information to customers
  • Complete EU MDR Pre-incoming inspections
  • Prepare the documentation required for custom clearance
  • Participate in the assessments of the new or updated regulations and standards applicable to the products, and national laws for any new or updated revisions. Communicate updates to regulatory staff.
  • Prepare, review, approve, distribution and training on QMS documentation.
  • Give support to Medicovigilance (FSCA (Recalls) and FSN for EU area).

What you'll need:

  • University degree in health of life science related subject.
  • 4 years in practical international medical device regulatory and quality experience. Experience with medical devices or similar is preferred.
  • Certified Quality Auditor (CQA) preferred.
  • Fluent in English & Spanish. Other languages is a plus.
  • MS Office.

What we offer:

Working in a diverse and collaborative global team embracing innovative curiosity, personal authenticity, accountability, and a growth mindset. Our culture empowers us to bring our whole selves to work each day, so we can be at our best when serving our customers, patients, and colleagues.

ZimVie offers you a challenging position with good career prospects in an international medical device business and following benefits:

  • Competitive compensation package.
  • Temporary contract until December 31, 2025
  • Meal allowance
  • Partially remote work option available
  • Learning & development program
  • Employee Assistance Program (EAP)

Do you want to know more about us?ClickHEREto watch our story.

ZimVie is an Equal Opportunity Employer committed to diversity and inclusion in the workplace. All qualified applicants for employment and employment decisions, including hiring, promotion, transfer, etc. are considered without regard to racial or ethnic origin, gender, religion or belief, disability, age or sexual identity.

ZimVie generally does not sponsor applicant work visas for this position.

  • Requisition ID: 3187
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