Bachelors degree degree of science in biology with master to work at cancer research center Empleos en Valencia

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!

Principal Duties and Responsibilities :

As a Quality Engineer, your responsibilities will be :

• Support the validation activities related to facilities, equipment, processes and computer systems as established in the internal procedures of the Quality System.
• Coordinate and conduct preventive and corrective actions (CAPAs), product controls, process and system changes (Engineering Change Request - ECRs and DCRs) from the perspective of Quality Assurance and carry out derived actions.
• Participate in production transfer projects (Transfer-in Transfer-out).
• Make modifications and updates to internal documents as a consequence of the implementation of global procedures and other changes.
• Participate in projects for the industrialization for new products and processes. Take part in OPPs (Operating Project Plan) and Lean Manufacturing projects.
• Conduct product non-conformities, process and quality system according to internal procedures.
• Review product reprocesses (reworks and revisions).
• Control equipment out of specifications, according to internal procedures.
• Take part in the development of Quality Holds and product quarantines.
• Generate control plans and guidelines for the different products and processes.
• Write and run TMVs (Test Method Validations).
• Manage temporary authorizations (TAs) and interim controls (ICs).
• Collaborate in PFMEAs investigations (Process Failure Mode Effects and Analysis) and document DMRs (Device Master Records).
• Analyze deviations of manufactured products.
• Provide data for indicator reports for Quality Assurance activities.
• Carry out internal audits of the Quality System and participate in external audits.

Education / Experience Requirements :

The ideal candidate should meet the requirements for this role, and we expect from you :

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 :

Are you interested? Apply online enclosing your cover letter, CV and references via our homepage. We look forward to receiving your application!

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, demotion, evaluation, compensation, and separation, are considered without regard to race, color, religion, religious beliefs, creed, national origin, ancestry, citizenship status, age, gender / sex (including pregnancy, childbirth, related medical conditions, lactation and breastfeeding), gender identity or expression (including transgender status), sexual orientation, marital status, military status, protected veteran status, disability, protected medical condition as defined by applicable state or local law, genetic information, or any other status protected under applicable federal, state and local laws.

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