Process Engineer - GMP Quality & Process Improvement

Zoetis Spain SL; Union City, Northern (CA, KY); Hybrid; USD 77,000 - 118,000; Full time

Benefits offered by this job

Healthcare benefits

401K with match

4 weeks vacation

Job summary

Zoetis is seeking a process engineering professional to lead CAPA investigations and drive continuous improvement in a GMP manufacturing environment. The role emphasizes risk-based validation, cross-functional collaboration, and ensuring high-quality consumables for diagnostic products.

Ideal candidates will have a BS in science/engineering, 5+ years GMP experience, and proficiency with Lean/Six Sigma and DOE. On-site work in a manufacturing setting is required.

Qualifications

• Requires BS in a science/engineering field with 5+ years GMP manufacturing experience.
• Advanced degree or certs in Process Engineering preferred.
• Lean/Six Sigma methods and project management experience valued.

Responsibilities

• Lead nonconformance investigations and CAPA using RCA and Lean Six Sigma.
• Support manufacturing and troubleshoot process-related issues.
• Lead projects to develop/optimize consumables for diagnostic products.
• Initiate change controls and perform risk assessments for improvements.
• Assist vendors with deviations and CAPAs to meet timelines.
• Develop protocols/reports for quality equipment/processes.
• Apply risk-based validation strategies with defined acceptance criteria.
• Collaborate with operations to boost production capacity and savings.
• Support continuous improvement initiatives and supplier qualification.

Skills

cGMP knowledge

Lean Six Sigma

Project management

team & independent work

DOE / statistical analysis

data-driven decisions

communication skills

English proficiency

MS Office suite

Education

BS in Science or Engineering (Mechanical/ Chemical preferred)

Job description

Zoetis is seeking a process engineering professional to lead CAPA investigations and drive continuous improvement in a GMP manufacturing environment. The role emphasizes risk-based validation, cross-functional collaboration, and ensuring high-quality consumables for diagnostic products.

Ideal candidates will have a BS in science/engineering, 5+ years GMP experience, and proficiency with Lean/Six Sigma and DOE. On-site work in a manufacturing setting is required.