Reference: 631821Posted: 2026-10-19Location: Mounds View, MNCompany: Planet Pharma GroupContact: ApplicationsEmail: applications@staffingfuture.comCan you please confirm your top 3 skills sets required? Experience in a regulated industry. Knowledge of international and domestic regulations associated with biocompatibility. Experience with assessing biocompatibility risk per ISO 10993 standards. Can you please confirm the 3 main responsibilities/day to day activities required for this role? Design and execute biocompatibility assessment plans and reports in accordance with ISO 10993 and regulatory requirements. Support product development lifecycle activities, including design changes and post-market surveillance, from a biocompatibility perspective. Interface with laboratories to coordinate testing activities, ensure compliance, and resolve any technical issues. What products (if any) will this role support? All products across EPT (CRM and CAS) What is your target years of experience? 5+ years _______________________________________________________________________________________________POSITION DESCRIPTION:The individual in this position is responsible for evaluating the safety and compatibility of medical devices with biological systems. The role involves planning and placing biocompatibility testing in accordance with ISO 10993 standards, regulatory guidelines, and risk assessment principles. This individual collaborates with cross-functional teams to ensure materials meet safety requirements. This individual analyzes data, prepares technical reports, and supports regulatory submissions. This position may also be involved in developing strategies for new products and addressing biocompatibility related issues during product development and post-market activities.POSITION RESPONSIBILITIES: Design and execute biocompatibility assessment plans and reports in accordance with ISO 10993 and regulatory requirements.Interface with laboratories to coordinate testing activities, ensure compliance, and resolve any technical issues.Review and interpret laboratory test results; document findings in technical reports and regulatory submissions.Support product development lifecycle activities, including design changes and post-market surveillance, from a biocompatibility perspective. Stay current with evolving global biocompatibility standards, guidance documents, and regulatory expectations to ensure ongoing compliance.Requires a University Degree and minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years relevant experience.
...Harvest Homes LLC is looking for a compassionate and dedicated Weekend Shift Group Home Worker (Friday, Saturday, Sunday - 1st Shift,... ...required Document resident behaviors, incidents, and any notable overnight observations accurately Respond calmly and effectively to...
...the lives of at-risk youth! Rite of Passage Team is hiring for a Teacher at Childhelp, Alice C. Tyler Village in Lignum, Virginia... ...Paid Time off available immediately for 20 Scheduled days for school breaks and 7 additional days to use at your diecretion and more...
...Job Description Job Description Immigration Attorney, Reston, VA Boutique Immigration Law Firm with busy nationwide practice has opening for associate attorney. Candidates must have minimum 2-5 years experience in business immigration law, including H-1B, L-1, TN...
...Radiology Technologist position is available in the Intensive Care Unit Electronic Remote Critical Care specialty at a facility in Florida. This role... ...interventional radiology procedures within a multi-campus healthcare organization. The position is designed for a highly...
...Join our team of professional educators! St Paul Christian School in Niceville, Florida, is a Christian school serving students in... ...achieve academic success. We are seeking an experienced PE teacher to implement a dynamic PE curriculum. Our PE teacher will utilize...