Senior Engineer — Pharma Process & Validation Leader

CIS International LLC; Juncos (PR); On-site; USD 90,000 - 120,000; Full time

Job summary

CIS International LLC in Juncos, PR seeks an experienced engineer to lead and oversee process optimization strategies, troubleshoot operational issues, and direct major system modifications in manufacturing and capital projects.

The role requires doctorate or masters with experience, collaboration across departments, and a track record in commissioning, validation, and compliant documentation within GMP/GLP environments.

Qualifications

• Experience with commissioning and qualification of parenteral products and related validation activities.
• Proven ability to develop engineering solutions for complex, regulated environments.
• Strong documentation and compliance with GLP/GMP requirements.

Responsibilities

• Characterize and optimize processes in operations, manufacturing, or capital projects.
• Direct design modifications and major system projects with cross‑functional teams.
• Develop results analyses and present interpretations for significant operational issues.

Skills

Pharma/biotech processes

GLP/GMP knowledge

Validation processes

Equipment operation

Technical report writing

Education

Doctorate or Masters + 2 years of Engineering experience

Bachelors in Engineering + 4 years of Engineering experience

Job description

CIS International LLC in Juncos, PR seeks an experienced engineer to lead and oversee process optimization strategies, troubleshoot operational issues, and direct major system modifications in manufacturing and capital projects.

The role requires doctorate or masters with experience, collaboration across departments, and a track record in commissioning, validation, and compliant documentation within GMP/GLP environments.