We are ZimVie, a integral 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
Por favor, asegúrese de leer completamente el resumen y los requisitos de esta oportunidad de empleo que se detallan a continuación.
About the role:
Ensure quality in both the process and the finished product, as well as compliance with the quality standards established by the organization.
Main responsibilities:
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- Participate in both internal Quality System audits and external audits.
- Manage preventive and corrective actions (CAPAs).
- Provide support for the validation of facilities, equipment, processes,
and IT systems in accordance with the Quality System’s internal procedures.
- Develop and execute Test Method Validations (TMVs) and Software Validations.
- Manage and review change control for products, processes, and systems from a Quality Assurance perspective and implement the resulting actions.
- Provide support in managing Health Hazard Evaluations (HHE) and Health Hazard Evaluation Determinations (HHED), product holds (internal/external), and product quarantines.
- Participate in production transfer projects (Transfer-in or Transfer-out).
- Provide support in investigating complaints regarding products manufactured at ZimVie Spain when requested by the Legal Manufacturer.
- Have recently earned a university degree in Engineering (or similar) and have less than 2 years of work experience, or hold an Advanced Vocational Degree and have more than 1 year of experience at ZimVie performing duties