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About ZimVie
Welcome to ZimVie, a new, publicly traded global company focused on improving quality of life for our patients. Our company is founded on a legacy of established brands, medical experts, and over $1B in annual revenue. We design, manufacture, and distribute a comprehensive portfolio of innovative solutions for implant dentistry, spinal surgery, and bone growth stimulation. Our seasoned leadership and dedicated global team of more than 2,500 are focused on shaping an exciting future for ZimVie — we hope you’ll consider being a part of it!
We believe everyone deserves to feel better, healthier, and stronger. That’s why we’re creating solutions for people to enjoy and experience life. Our culture empowers us to bring our whole selves to work each day, serving colleagues, customers, investors, and communities.
About The Role
Working at ZimVie is purpose-driven. Every day, you use your talents to create solutions for people to enjoy life. We are seeking a talented Microbiologist to join our team in Valencia, responsible for ensuring finished products meet cleanliness, sterility, and biocompatibility standards.
What You’ll Be Doing
* Coordinate microbiology activities including documentation and testing of products, processes, and facilities.
* Manage clean room monitoring, sterilization validations, and dose audits.
* Oversee water and compressed air monitoring activities.
* Conduct biological studies for biocompatibility evaluations.
* Report monthly KPIs based on data analysis.
* Act as liaison with external microbiological laboratories.
* Support transfer-in and new product introduction projects.
* Participate in validation activities of facilities, equipment, and processes.
* Review product, process, and system changes from a microbiological perspective.
* Coordinate CAPAs related to microbiology.
* Update and improve local documents based on global procedures and regulations.
* Lead or support operational project plans related to manufacturing processes.
* Manage non-conformities, product blockages, and quarantines.
* Prepare Temporary Authorizations and participate in risk assessments.
* Conduct internal audits and serve as SME during external audits.
What You’ll Need
* 3-5 years’ experience in a similar role, preferably in a multinational environment.
* Qualifications in a related field.
* Knowledge of ISO 9001, ISO 13485, MDR 2017/745, and 21 CFR Part 820.
* Fluency in Spanish and English.
* Proficiency in MS Office, especially Excel.
* Strong planning, organization, decision-making, and problem-solving skills.
What We Offer
Our benefits and programs support your well-being inside and outside of work—because you’re worth it.
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