Quality Assurance Engineer
Summary
Lead and enhance pharmaceutical quality system activities—including investigating deviations, complaints, and out-of-specification events, writing protocols, conducting risk assessments, and managing CAPAs—to strengthen inspection readiness and process robustness at a contract manufacturer of OTC, dietary supplement, and prescription products.
The Quality Systems Engineer is a key member of the Quality Assurance unit, responsible for leading and enhancing quality system activities including but not limited to quality event investigations (deviations, complaints, con-conformances and OOS) protocol writing (reworks and reprocessing) risk assessments and CAPAs. The Quality Systems Engineer 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
Work Hours: Monday-Friday 8:00AM-4:00PM
Pay Range: $80,000 - $110,000 per year, depending on experience
Start Date: ASAP
Why Join CPC?
At CPC, you’ll be part of a team that has set the standard in pharmaceutical development and contract manufacturing since 1971, helping bring high-quality OTC, dietary supplement, and prescription products to market faster and safer than ever. We pride ourselves on quality as a core value, innovative problem-solving, and a collaborative culture where everyone plays a role in advancing formulation and manufacturing excellence. CPC offers an inclusive, respectful workplace with opportunities to grow your skills and career while working with cutting-edge technologies and serving leading global brands. With a commitment to employee success, competitive benefits, and a culture built on teamwork and integrity, CPC is a place where your contributions truly make an impact.