RA QA SPECIALIST

Experience Required:

Minimum 3

Years Education:

Bachelor's Degree Preferred We are seeking a detail-oriented and experienced Quality Assurance Specialist to support quality operations and compliance initiatives in a regulated environment. This individual contributor role requires sound professional judgment, the ability to work independently with minimal supervision, and a strong understanding of quality systems, regulatory compliance, and process improvement. The ideal candidate will have hands-on experience implementing quality standards, supporting audits and inspections, and ensuring compliance throughout all stages of operational and production processes. This position is an on-site office position. Must live in the local area. Key Responsibilities Implement and maintain quality standards across all stages of the process Ensure compliance with internal procedures, regulatory requirements, and quality systems Assess potential quality and compliance risks and provide recommendations for mitigation Take ownership of quality control activities related to: Service Processes Testing and operations Production processes Finished products and services Facilitate internal audits and regulatory inspections Coordinate and support quality training initiatives Apply professional expertise and independent judgment to resolve quality-related issues Collaborate cross-functionally to drive continuous improvement and compliance excellence Qualifications Bachelor's degree preferred or equivalent in experience Minimum of 3 years of relevant quality assurance or quality control experience Strong understanding of quality systems, compliance standards, and regulated environments Experience supporting audits and regulatory inspections Ability to work independently with minimal supervision Strong analytical, organizational, and communication skills Practical knowledge gained through hands-on industry experience preferred Preferred Skills Experience in medical device, pharmaceutical, biotech, or healthcare environments Familiarity with GMP, GLP, GCP, FDA, or ISO standards Strong problem-solving and risk assessment capabilities