Zimmer Biomet is a global medical technology Our team members are part of a company with a heritage of leadership, a focus on shaping the future, and a mission dedicated to alleviating pain and improving the quality of life for people around the Job Summary A collaborator who is responsible for the local / regional QMS and all the activities related to Quality controls and documents such as local procedures, work instructions, quality holds, field actions, complaints, internal audits in the warehouse and audits at local third parties like distributors and service This role is also responsible for local labeling, pest control and to establish storage and transport conditions for all part numbers, as well as expiration date control and non-conformities and Principal Duties and Responsibilities Acts as the Quality responsible, controlling daily work activities, communicating with other departments and problem Establishes local standard operational procedures in Spanish based on GBL procedures and local Work on local complaints, recalls, field actions and quality hold reporting to the manufacturers in a timely Act as postmarket (Technovigilance) Assess and conduct local complaint Prepares and submit periodic safety Conduct local training to the Perform finished goods labeling and shipment inspection of catalog items Audits ZB local warehouse as well as distributors and service Opens non-conformities and CAPAs as needed and proceed with root cause analysis and investigation to close Guarantee that the ERP systems are updated for local Keep track of local labeling by PN and lot Establishes and updates local risk Schedules QMS management review with stakeholders and the general manager twice a Assist various departments with document retrieval as Generates reports, analyzes tends and performs other duties, as Support to QA/RA Manager responsible with audits from government (Ministry of Health, CCSS) Education/Experience Requirements Bachelor's degree: Chemical, Pharmaceutical, Industry, Alternate degrees may be considered Registered in the local professional English Proficiency is 3-5 years of experience in orthopedic or medical device industry preferred 3-5 years of experience in Regulatory Affairs, Engineering, Quality, or related field required International standards such as: ISO 13485, ISO 9001, Local standards, Decree No 34482-S, Decree 41387-S and applicable standards for medical device distribution Technovigilance Travel Requirements 5% EOE/M/F/Vet/Disability
