We’re looking for a Quality Assurance Engineer Director who is a key member of the Quality Assurance unit within a pharmaceutical manufacturing environment. This role is responsible for technical leadership and enhancement of quality system activities including but not limited to, quality event investigations (deviations, complaints, non-conformances, and OOS), protocol writing (reworks and reprocessing), Annual Product Reviews, Stability Protocol and Report, Risk Assessments and CAPAs. The Quality Assurance Engineer Director oversees a team that applies engineering, analytical, and risk-based thinking to identify systemic issues, improve process robustness, and strengthen inspection readiness. 

• Job Type: Full-Time
• Location: Hauppauge, NY
• Level: Director
• Works Hours: Monday – Friday, 8:00AM – 4:00PM EST
• Pay Range: $125,000 - $150,000 per year, depending on experience and level
• Start Date: ASAP

What makes this role exciting

• This role sits at the intersection of quality, leadership, compliance and impact 
• Define quality engineering strategies and lead cross-functional teams
• Review advanced analytics and help modernize manufacturing systems 
• Serve as the subject matter expert on data aggregation and analysis for the company’s annual product review, continuous process verification and stability programs

Responsibilities: Include, but are not limited to: 

· Leads a team that author complex quality event investigations (deviations, complaints, non-conformances, and OOS), protocols (reworks and reprocessing), risk assessments and CAPAs.

· Apply structured problem-solving methodologies (e.g., lean and six-sigma, DMAIC, root cause analysis, FMEA, fishbone, 5-Why) to drive high-quality, defensible conclusions.

· Ensure all documentation meets cGMP, FDA, EMA, and internal quality standards, with a focus on clarity, logic, and inspection-ready narratives.

· Review and challenge investigation content prepared by cross-functional teams to elevate overall quality and consistency.

· Drive the development of robust, risk-based CAPAs that address true root causes rather than symptoms.

· Assess CAPA effectiveness and sustainability; identify trends and opportunities for system-level improvements.

· Coach and mentor Quality Engineer and related QA staff by modeling industry standard investigation practices.

· Analyze trends across quality vents to identify systemic risks, recurring failure modes, and opportunities for process improvement.

· Support continuous improvement initiatives by translating quality data into actionable insights.

· Contribute to the design or enhancement of quality processes, templates, and tools to improve investigation quality and efficiency.

· Serve as a thought partner to operations and technical teams during issue resolution and change management activities.

· Act as a trusted QA partner to external customer and internal departments including Manufacturing, Packaging, Engineering, Technical Operations, Accounts Management, and Supply Chain.

· Provide risk-based quality input to support sound business decisions while maintaining regulatory compliance.

· Support inspection readiness activities, including responses to regulatory questions related to investigations and CAPAs.

· Complete internal audits and support external audits of CPC operations.