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: Project Support New biocompatibility strategy – strategy and implementation of a new Document System and Structure to satisfy global biocompatibility requirements.What you'll be doing: Participate in a specific Project of Zimvie's Quality & Microbiology Area associated with the standards and biocompatibility requirements of medical devices according to ISO 10993. Review and analyze the historical documentation of the Quality System to obtain the inputs that allow the design and optimization of the company's new strategy in terms of compliance with biocompatibility requirements.The documents to review would be, but not limited to, risk analysis reports, manufacturing procedures, production process flows, validations of production processes, material specifications, packaging, etc., contact materials involved in production, safety data sheets.Write procedures and work instructions related to the project.Drafting and execution of Biological Evaluation Plans and Reports (BEP/BER) Coordination of consulting activities and/or laboratory tests associated with biocompatibility requirements with laboratories and specialized companies.What you'll need: Be in possession of a university degree in Engineering, Biology, Biotechnology, Toxicology, or similar.Desirable training or experience in the area of ??Microbiology or Toxicology.Possess a minimum of 1 year of professional experience Possess a high level of English, both spoken and written.Essential It is essential to have knowledge in the use of office tools.It is desirable to have basic knowledge of biocompatibility in medical devices according to ISO 10993 (optional) 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 the end of the year Meal alowance Partially remote work option available Private life, health and dental insurance Learning & development program 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.
