Share Email Opening Title Director of QA  About the Organization Acutis (www.Acutis.com) is a specialized medical laboratory that complements its hard science with the soft skills of its support teams. This combination allows practitioners to diagnose and treat with greater confidence and with ease. At Acutis Diagnostics, we are dedicated to providing accurate and reliable clinical diagnostics services to healthcare providers, patients, and communities. As a leading laboratory specializing in toxicology testing and molecular-based PCR tests, we are committed to delivering timely and precise results that aid in patient care and treatment decisions. Founded on the principles of thorough, exact, consistent results, Acutis Diagnostics leverages cutting-edge technology and the expertise of our highly skilled team to deliver exceptional service and support to our clients. We understand the critical role diagnostic testing plays in healthcare, and we prioritize quality and accuracy in every step of our process. Whether it's toxicology screening to detect substance abuse or molecular PCR testing for infectious diseases, we strive for excellence in every test we perform. Above all, our mission at Acutis Diagnostics is to improve patient outcomes and enhance public health through advanced diagnostic solutions. We are proud to be at the forefront of clinical diagnostics, contributing to the advancement of medicine and the well-being of patients at large.   EOE Statement We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.   Description Acutis Diagnostics is a growing clinical laboratory with locations in Hicksville, NY and Monmouth Junction, NJ. We pride ourselves on providing expert, accurate and concise results as a product of our highly talented and passionate team of professionals. We believe the team we build today will be the foundation of our future success. Working with the Clinical Laboratory Director(s), the Quality Assurance Director will be responsible for creating and maintaining a Quality plan and quality management system (QMS) which will be compliant with CLIA, CAP. NYSDOH, and FDA (whenever applicable) guidance and standards. The QA director will ensure that quality standards are being met, and any deviation from an applicable protocol, standard or guideline has been adequately investigated and addressed. Provides QA expertise to the laboratory and as needed, serves as the liaison to external governing entities. The Quality Assurance Director ensures that the laboratory and the laboratory staff follow all laws and regulations that are required by CLIA, CAP, OSHA and NYSDOH and any other applicable legislative organizations, and raise any related issues to the upper management in real time. In addition to performing the role by him/herself., the Quality Assurance Director will oversee a QA team and work cooperatively to integrate and maintain an efficient QMS, provide all needed training and make the organization inspection ready at any moment. Responsibilities Develop and implement a quality strategic plan for the QMS to successfully support lab developed tests (LDT) and FDA-approved IVD medical devices including software algorithms intended to provide patient information and support. Provide QA leadership/mentorship for QA team and cross-functionally. Ensure QMS areas are adequately supported and resourced. Partnering with the lab director(s) and other stakeholders, develop and implement policies and procedures and train lab staff on them. Maintain company compliance to CAP/CLIA regulations for LDT, NYSDOH and other state regulation and 21 CFR 820 when applicable. Improve internal and external customer satisfaction through Quality initiatives, establishing QA metrics and process improvement. Collaborate closely and effectively with R&D and Operations to ensure end to end oversight of Quality technical activities so that evidence is generated, essentially that plans are created, assessed, reviewed, and issues are mitigated as appropriate. Provide leadership and support for any internal, customer, regulatory body, or health authority audits/inspections. Lead and/ or support compilation and articulation of nonconformances with the implementation of best-practice corrective action and preventive action plans (CAPAs) to bring any issue to resolution as fast as practical. Oversee and drive refinement of training program requirements, document control and supplier quality activities to build in increased effectiveness. Oversee training and education of Quality throughout the organization and build collaborative relationships with key stakeholders. Collaborate with the Clinical Laboratory Director, Director of Operations and Quality Team to optimize and enforce the Quality Plan as it is written. Maintain a state of readiness for inspections, through regular periodic meetings with all department Directors and supervisors, self-inspection check lists and proactive observation. Prioritize responsibilities, anticipates problems, and provides timely and appropriate solutions. Able to act as a liaison with other operational areas to get an QA issues resolved.   Position Requirements Education requirement BSc, MSc, or PhD in life Science, medical technology, chemistry or engineering. NYS CLT License (preferred) 10+ years of experience in QA implementing and/or maintaining quality management systems in a regulated clinical laboratory or an IVD company. 5+ years of experience in a lab providing services to pharma and biotech companies in clinical trials. Experience and Skills Required Experience building and leading high performing teams, including direct-report managers. Ability to interact with all levels of colleagues to educate and inform on the utility the QMS, in turn driving compliance and continuous improvement. Ability to drive continuous monitoring and process improvement to build collaborative efficiencies. Ability to drive a culture of solution-oriented and evidence-based mind-sets with openness for innovative ways of working. Ability to lead cross-functional teams in problem-solving and execution. Experience in the areas of laboratory supervision and workflow needs and technical capabilities Experience working with Quality Management including strong knowledge of all laws and regulations that are required by CLIA, CAP, OSHA and other related legislative and/or state health departments and organizations. Excellent professional communication skills, including verbal, written, and presentation Excellent collaboration skills, with the ability to positively influence others Computer proficient with multiple software programs, including MS Office Suite, and Laboratory Management Systems Must have willingness to travel to Hicksville, N.Y. on occasion. Ability to commute/relocate: Monmouth Junction, NJ 08852: Reliably commute or planning to relocate before starting work (Required) Education Requirements: Bachelor's (Required) Experience Requirements: QA/QC: 10 years (Required) Lab/ BioPharma: 5 years (Required)   Full-Time/Part-Time Full-Time   Location Acutis BioSciences - NJ   This position is currently not accepting applications. 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