The Sr. Associate II, Compliance plays a critical leadership role in ensuring the RTP Drug Substance Manufacturing site maintains a strong state of compliance and inspection readiness. This position partners closely with Site Leadership and Quality teams to oversee inspection management, data integrity, and quality systems, while driving continuous improvement across local and global processes. This role is instrumental in ensuring adherence to regulatory requirements and strengthening a culture of quality and compliance across the organization. What You’ll Do. Lead site compliance and inspection management activities, including planning, execution, and regulatory response coordination. Ensure the site remains inspection-ready at all times for domestic and international regulatory agencies. Provide compliance oversight across data integrity, risk management, and quality systems. Prepare and facilitate site governance meetings and deliver quality metrics using tools such as Veeva, Track. Wise, and Power BI - Drive quality management review processes and lead quality metric governance to support data-driven decision making. Partner with global quality forums to ensure alignment with the global Quality Management System (QMS)Lead and support process and product risk assessments, ensuring timely completion and effectiveness. Identify and proactively resolve compliance gaps and technical issues. Champion continuous improvement initiatives across quality systems and processes. Serve as a key Quality representative on cross-functional teams and site leadership initiatives. Who You Are. You are a proactive and detail-oriented quality professional with a strong foundation in compliance and regulatory expectations. You bring a continuous improvement mindset and thrive in fast-paced, highly regulated environments where collaboration and data-driven decisions are essential. Required Skills. Bachelor’s degree in scientific, technical, or relevant discipline. At minimum 5 years of Quality Assurance experience in pharmaceutical, biotech, or manufacturing environments. Strong knowledge of cGMP regulations and global regulatory standards (FDA, EMA, etc.)Experience with inspection management, compliance oversight, and quality systems. Demonstrated ability to analyze data, manage risk, and support regulatory interactions. Excellent communication, organizational, and problem-solving skills. Ability to manage multiple priorities and make decisions under pressure. Preferred Skills. Prior experience in Compliance-focused Quality roles. Experience with quality systems such as Veeva, Track. Wise, and Power BI - Strong knowledge of data integrity principles and regulatory expectations. Experience supporting global quality initiatives and cross-functional teams. Proven ability to drive continuous improvement and influence stakeholders Job Level: Professional.