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Multi-site Dermatology Group Seeks Laboratory Operations and Quality Manager Optima Dermatology is recruiting an experienced Laboratory Operations and Quality Manager to join our growing Dermatology and Medical Aesthetics group in Portsmouth, NH.  Location: 111 NH Ave, Portsmouth, NH 03801 Position Summary The Laboratory Operations & Quality Manager oversees the day-to-day operations of the Histology Laboratory while developing and maintaining its Quality Management System (QMS). Reporting directly to the Laboratory Operations Director, this role ensures the lab runs efficiently, safely, and in full compliance with regulatory and accreditation requirements. The manager serves as the operational leader on the floor — coordinating staffing, workflow, and equipment — and as the lab's quality authority, driving continuous improvement and inspection readiness. This position partners closely with technical staff, pathologists, and organizational leadership.   Responsibilities: The following is an overview of the essential job functions and responsibilities; this may not be an all-encompassing list:   Laboratory Operations Oversee daily laboratory operations, including specimen workflow, turnaround times, staffing coverage, and scheduling. Serve as the primary point of escalation for operational issues on the floor. Monitor and manage productivity, capacity, and workflow efficiency; adjust processes as volume grows. Coordinate with pathologists and clinical teams to ensure smooth specimen handling from receipt through reporting. Manage supply inventory, vendor relationships, and equipment maintenance schedules. Support laboratory expansion, relocation, and new-service initiatives as directed by the Laboratory Director. Quality Management & Regulatory Compliance Develop, implement, and maintain the laboratory QMS. Ensure compliance with CLIA, CAP, OSHA, HIPAA, state, and other applicable regulatory requirements. Maintain continuous inspection readiness; coordinate accreditation activities and responses to findings. Manage document control — policies, procedures, forms, and quality records. Oversee occurrence reporting, root cause analysis, and corrective/preventive actions (CAPA) through completion. Track, trend, and report quality metrics to laboratory leadership. Process Improvement & Validation Lead internal audits and process assessments; identify and execute improvement opportunities. Coordinate validation and verification studies for new instruments, equipment, assays, and software. Review quality control and proficiency testing data for compliance and performance. People & Training Supervise designated laboratory personnel; support hiring, onboarding, and performance management in partnership with the Laboratory Operations Director. Monitor staff competency assessments and coordinate quality-related training. Promote a culture of accountability, patient safety, and continuous improvement. Risk Management Conduct risk assessments for laboratory processes. Investigate quality incidents, complaints, and nonconformances; develop and monitor action plans. Supervisory Responsibilities Supervises histology laboratory technical and support staff as designated; may oversee quality coordinators or specialists as the team grows.   Qualifications: Education Bachelor’s degree in Medical Laboratory Science, Histotechnology, Biology, Chemistry, or a related scientific field required; Master’s degree preferred. Certifications HTL(ASCP) or HT(ASCP) preferred; MLS(ASCP), QIHC(ASCP), or CPHQ a plus. Experience 5+ years of progressively responsible experience in a histology or anatomic pathology laboratory required. 2–3+ years of laboratory supervisory or management experience strongly preferred. Hands-on experience with CAP/CLIA compliance and