# Investigation Sr. Specialist at bioMerieux in Hazelwood,… > Investigation Sr. Specialist at bioMerieux in Hazelwood, Missouri, United States. Category: Operations Jobs. View full job details and apply now on… Investigation Sr. Specialist # Investigation Sr. Specialist bioMerieux ## Job Description Position Summary The Investigation Senior Specialist supports post-market quality activities by conducting investigations, evaluating product performance data, and identifying trends that may impact product quality, reliability, or compliance. This role collaborates cross-functionally to assess product risks, support corrective and preventive actions (CAPA), and ensure compliance with applicable regulatory requirements and quality system standards. Primary Responsibilities - Conduct investigations of product complaints, adverse events, and quality issues to determine root causes and recommend appropriate actions. - Analyze complaint, service, QC, manufacturing, and field performance data to identify trends and emerging risks. - Monitor and maintain surveillance dashboards and reliability metrics to support post-market monitoring activities. - Perform risk assessments and provide recommendations for product quality improvements. - Support CAPA activities, effectiveness checks, and continuous improvement initiatives. - Collaborate with Quality, Regulatory Affairs, Manufacturing, R&D, Technical Support, and other cross-functional teams to resolve quality concerns. - Prepare and present investigation findings, trend reports, and recommendations to internal stakeholders. - Support internal and external audits, inspections, and regulatory inquiries. - Develop and maintain standard operating procedures (SOPs), work instructions, and related documentation. - Represent Post-Market Quality on cross-functional projects as assigned. - Perform other duties as assigned. Qualifications Minimum Required Qualifications - Bachelor's degree in Life Sciences, Biology, Chemistry, Biomedical Sciences, Biotechnology, Engineering, or Medical Laboratory Science related degree required. - 5+ years of experience with complaint handling, investigations, post-market surveillance, quality systems, or risk management in a Quality, Regulatory, Manufacturing, Medical Device, IVD, Life Sciences, or a related regulated industry required. Preferred Qualifications - Medical Device and/or In Vitro Diagnostics (IVD) industry experience strongly preferred. Knowledge, Skills & Competencies - Strong analytical and critical-thinking skills. - Excellent written and verbal communication skills. - Ability to interpret and analyze complex technical and quality data. - Demonstrated problem-solving and root-cause investigation capabilities. - Strong attention to detail and organizational skills. - Ability to work effectively in a cross-functional environment. - Proficiency with Microsoft Office applications. - Knowledge of quality and regulatory requirements applicable to medical devices and IVD products, including FDA and ISO standards. - Continuous improvement mindset with the ability to drive process enhancements. Working Conditions - Primarily office-based with periodic work in manufacturing, laboratory, or operational areas. - Ability to sit, stand, and move throughout facility locations as needed. - Occasional domestic and international travel may be required. - Ability to lift and move light materials as required by the position. Advertisement Posted November 1, 2026 ## Related Jobs Assistant Manager I Family Dollar Manager Production Tech 1 - 2nd Shift bioMerieux Full Time Instrument Repair Center Technician bioMerieux Full Time Instrument Repair Center Technician bioMerieux Full Time Investigation Sr. Specialist bioMerieux Senior Instrument Repair Technician (Swing Shift) bioMerieux Full Time Instrument Repair Technician (Swing Shift) bioMerieux Full Time Insurance Producer - Austin, TX Horace Mann Full Time ## Related Searches