About this opportunity : The Quality Assurance Compliance Specialist is responsible to supporting the site’s regulatory intelligence compliance and auditing functions. This position provides regulatory compliance management within the Quality organization. Key Responsibilities: • Support inspection administration during Health Authority and client inspections. • Support Avecia’s Health Authority and client audits to identify potential risks, including approval of any final reports and completion of identified CAPAs. • Provide administrative and operational support within the Quality Assurance Department, including the retrieval, organization, and management of quality documents, records, and data to support and ad hoc documentation requests. • Participate in the preparation or review of responses to Health authority and client inspectional observations. • Support the execution of commitments identified during Health Authority and client audits and ensure that CAPAs are closely monitored and completed in a timely fashion. • Support the compilation of Nitto Avecia’s KPI metric requirements and Management Review process by compiling, and trending quality data related to audit findings. • Maintain Site Master File and issue Letters of Authorization • Support Internal Audit Program: Perform and/or support Nitto Avecia internal audits to identify potential risks, including approval of any final reports and CAPAs, as needed. Required Skills/Abilities: • At least 5 years’ experience in a regulated/GMP industry required, with experience in Pharmaceuticals or Biotechnology preferred. • This position requires a candidate with regulatory inspection experience to lead Nitto Avecia’s inspection readiness program. • Comprehensive working knowledge of cGMP’s/FDA regulations, Quality systems, FDA Guidance documents, USP, ICH and other applicable laws and their interpretation, implementation • Proficient with PC-based word processors and spreadsheets. • Proficient with electronic quality management systems • Intermediate understanding of ICH, ISO, cGMP, USP, EU, and other relevant regulatory guidance/requirements. Specific knowledge of 21 CFR 210, 21 CFR 211, ICH Q7, ICH Q9, ICH Q10, Eudralex – Volume 4, is desired. • Ability to work in a fast-paced environment consisting of internal and external team members with minimal oversight. • Problem-solving skills with the ability to adapt to changing priorities and timelines. • Strong leadership and communication skills, including establishment of clear expectations and development of metrics and KQIs to monitor performance and ongoing activities. • Demonstrated ability to write effectively, present ideas publicly, and proactively share knowledge with others to encourage team development. • Ability to build positive working partnerships with other department management teams to successfully support validation and commissioning timelines. • Experienced with making decisions through critical reasoning to solve standard and involved problems that may impact multiple departments. • Experienced in the use of electronic systems such as eQMS • Prior experience with clinical and commercial manufacturing is preferred. • Requires the ability to gown into clean rooms and wear PPE. The annualized salary range for this position is between $71,500.00 and $87,500.00.