Looking to make a real impact in a fast-moving industry? As a Quality Engineer, you’ll play a crucial role in ensuring top-tier product quality and process efficiency. You’ll be at the heart of developing and implementing new processes, training teams, and driving continuous improvement—all within a GMP-regulated environment.

Why You Should Apply

• Lead quality initiatives in a cutting-edge manufacturing setting
• Gain hands-on experience in process development and implementation
• Work within a GMP-regulated environment, ensuring top-quality standards

What You’ll Be Doing

• Developing new quality processes, writing work instructions, and creating training plans
• Conducting training sessions and onboarding new team members across shifts
• Performing root cause analysis and corrective actions for process improvements
• Implementing Statistical Process Control (SPC) and Lean/Six Sigma methodologies
• Conducting audits and ensuring compliance with GMP and ISO 9000/AS9100 standards

About You

• Be able to do the job as described
• Strong experience in GMP, preferably in pharma manufacturing
• Skilled in statistical analysis, DOE, and process validation
• Proficient with Minitab or other statistical software
• Exceptional problem-solving and communication skills

How To Apply

We’d love to see your resume, but we don’t need it to have a conversation. Send an email to ccupo@jacobsmgt.com and tell me why you’re interested. Or, if you do have a resume ready, apply here.