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Associate Continuous Improvement Engineer
Perrigo Company plcContinuous Improvement Engineer supporting incident investigations and process improvements for Perrigo’s pharmaceutical manufacturing facilities in Michigan. Driving Lean Six Sigma and equipment-reliability initiatives across operations and maintenance.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in technical support for incident investigations and process improvements within pharmaceutical manufacturing, utilizing Lean Six Sigma methodologies and a strong understanding of cGMP and FDA regulations.
Highest-signal resume keywords
Lean Six Sigma MethodologiesPharmaceutical Sciences KnowledgeTechnical Writing SkillsCGMP and FDA Regulations FamiliaritySAP Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Incident InvestigationRoot Cause AnalysisCorrective and Preventive ActionsRisk AssessmentData AnalysisProcess ImprovementEquipment ReliabilityManufacturing Process KnowledgeAutonomous MaintenanceTotal Productive Maintenance
Soft Skills
Interpersonal SkillsOrganizational SkillsCommunication SkillsIndependent WorkProject Management
Tools & Technologies
Microsoft OfficeExcelWordSAP
Industry Keywords
CGMPFDA RegulationsContinuous ImprovementOperational ExcellenceTechnical Guidance
About the role
Key responsibilities & impact- Provide technical support for incident and deviation investigations for commercialized products at Perrigo facilities within Michigan
- Identify root causes of incidents and deviations
- Develop and implement corrective and preventive actions
- Collaborate with cross-functional teams to coordinate investigations and resolve issues promptly
- Conduct risk assessments to identify manufacturing-process improvements
- Use Lean Six Sigma methodologies and tools to drive continuous improvement
- Collect and analyze data to identify trends and improvement areas
- Stay current with industry best practices and technological advancements
- Support ODR activities by defining base equipment conditions, inspection points, and lubrication standards
- Partner with operations and maintenance to eliminate contamination sources and hard-to-access areas
- Provide technical guidance to strengthen equipment reliability and align ODR routines with continuous-improvement objectives
Requirements
What you’ll need- Bachelor’s degree, preferably in engineering, chemistry, pharmaceutical sciences, or a related field
- Knowledge of pharmaceutical sciences and manufacturing processes
- Well-developed interpersonal, organizational, and communication skills
- Ability to work effectively with staff members at all levels
- Strong technical writing skills
- Familiarity with cGMP and FDA regulations
- Familiarity with investigations and/or developing and recommending process improvements
- Experience with operator-focused reliability programs such as ODR, Autonomous Maintenance, or TPM preferred
- Computer literacy and working knowledge of Microsoft Office, including Excel and Word
- SAP experience preferred
- Ability to work independently on multiple concurrent projects with minimal guidance
- Ability to meet project deadlines
Benefits
Comp & perks- Competitive compensation
- Benefits tailored to supporting employees and their families
- Career development opportunities
- Inclusive, collaborative culture
- Equal opportunity employment