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CONMED is seeking a to support microbiology and sterilization-related quality systems for medical device manufacturing. This role provides hands-on quality engineering support across environmental monitoring, bioburden, sterilization validations, and compliance activities, while partnering closely with Manufacturing, Quality Assurance, Regulatory, and Operations teams. The position is ideal for an earlycareer quality professional with a foundation in microbiology or life sciences who is looking to grow in a regulated medical device environment. This position is fully onsite at our Utica, NY location. Key Responsibilities * Support microbiology and sterilization quality activities, includingEtO, Gamma, and EBeam dose setting, audits, annual assessments, and validations. * Coordinate and maintainenvironmental monitoring programs, including data trending, analysis, and continuous improvement actions. * Maintain and trendproduct bioburden and environmental samplingdata. * Assist in theidentification, investigation, and implementation of CAPAs, including root cause analysis and effectiveness checks. * Supportinternal, customer, and regulatory audits, including preparation, execution, and followup activities. * Executeinternal process auditsto ensure compliance with regulatory and quality system requirements. * Develop, review, and maintainprotocols, reports, and quality documentationrelated to microbiology and sterilization sciences. * Partner crossfunctionally to investigate and resolveprocess and product quality issues. * Support training activities related to microbiology, sterilization, and quality system processes. * Maintain current knowledge of applicableregulations, standards, and guidance documents. Required Qualifications * Bachelor's degreein Engineering, Microbiology, Chemistry, Biomedical Engineering, or a related scientific discipline. * 0-2 years of experiencein a regulated manufacturing or laboratory environment (medical device preferred). Preferred Qualifications * Foundational knowledge ofquality systems and problemsolving methodologies. * Ability to analyze data, identify trends, and support corrective actions. * Strong written and verbal communication skills. * Experience working in amedical device or regulated industry. * Working knowledge ofFDA QSR (21 CFR 820)andISO 13485. * Familiarity withISO 11135, ISO 11137, ISO 14644, or related microbiology/sterilization standards. * Handson experience withaseptic technique, laboratory sample collection, or environmental monitoring. * Exposure to quality tools such asCAPA, audits, validations, and root cause analysis. * Quality certifications (CQE, CQA, Lead Auditor) a plus, but not required. Why Join CONMED * Work in ahighimpact quality rolesupporting lifesaving medical devices. * Gain exposure tosterilization sciences and microbiologywithin a global medical device organization. * Opportunity forcareer growthwithin Quality Engineering and Quality Systems. * Collaborative culture focused oncontinuous improvement, compliance, and patient safety.Travel Expectations 0-20% This positionis not eligible for employer-visa sponsorship. Disclosure as required by applicable law, the annual salary range for this position is $67,496 - $97,240. The actual compensation may vary based on geographic location, work experience, education and skill level. The salary range is CONMED's good faith belief at the time of this posting. Benefits:CONMED offers a wide array of benefits to fit your unique needs. Visit our Benefits Pagefor more information. * Competitive compensation * Excellent healthcare including medical, dental, vision and prescription coverage * Short & long term disability plus life insurance -- cost paid fully by CONMED * Retirement Savings Plan (401K) -- CONMED matches your contributions do