Pharma CI Engineer: Lean Six Sigma & Process Optimization

Perrigo Company plc; Michigan; On-site; USD 85,000 - 110,000; Full time

Job summary

Perrigo Company plc is seeking a Continuous Improvement Engineer to provide technical support for incident and deviation investigations across Perrigo facilities in Michigan. You will identify root causes, develop CAPAs, and collaborate with cross-functional teams to ensure timely resolutions.

The role requires knowledge of cGMP and FDA regulations, plus experience with Lean Six Sigma and data-driven process improvements. Strong communication and writing skills are essential.

Qualifications

• Bachelor’s degree preferably in engineering, chemistry, pharmaceutical sciences or related field.
• Knowledge of pharmaceutical sciences and manufacturing processes.
• Strong interpersonal, organizational and communication skills, plus technical writing ability; familiarity with cGMP and FDA regulations.
• Experience with cGMP and FDA regulations, including investigations and process improvements.
• Computer literacy with MS Office and SAP experience preferred.
• Ability to manage multiple projects independently and meet deadlines.

Responsibilities

• Provide technical expertise to identify root causes of incidents and deviations.
• Develop and implement corrective and preventive actions to prevent recurrence.
• Collaborate with cross-functional teams to coordinate investigations and timely resolutions.
• Conduct risk assessments and apply Lean Six Sigma methodologies to drive improvements.
• Collect and analyze data to identify trends and areas for improvement.
• Stay current with industry best practices and technologies to enhance CI efforts.

Skills

Interpersonal skills

Communication skills

Technical writing

Education

Bachelor’s degree in a relevant field

Tools

SAP

Job description

Perrigo Company plc is seeking a Continuous Improvement Engineer to provide technical support for incident and deviation investigations across Perrigo facilities in Michigan. You will identify root causes, develop CAPAs, and collaborate with cross-functional teams to ensure timely resolutions.

The role requires knowledge of cGMP and FDA regulations, plus experience with Lean Six Sigma and data-driven process improvements. Strong communication and writing skills are essential.