Product Quality Specialist

Role: Product Quality Specialist focused on stability management within Johnson & Johnson's Innovative Medicine sector, overseeing product quality from late-stage development through full commercial lifecycle. Responsibilities: ensure stability integrity, develop and review stability protocols and reports, support regulatory filings, handle stability-related escalations, and mentor team members. Act as stability SME for complex or high-value product families, actively contribute to Stability Center of Excellence operations, and identify process improvements. Requirements: 6-8 years industry experience, Bachelor’s Degree, strong knowledge of stability regulations, proficiency in SOPs and protocols, and ability to work independently and cross-functionally. Preferred skills include business savvy, compliance management, problem solving, and familiarity with quality management systems like ISO 9001. High-Value: focus on stability within pharmaceutical products, supporting lifecycle management, regulatory compliance, and cross-functional collaboration. Work setup: based in Raritan or Titusville, NJ, with no travel specified.