Senior Process Engineer — Pharma Validation & Design

Cis-International-LLC; Juncos (PR); On-site; USD 80,000 - 120,000; Full time

Job summary

Cis-International-LLC in Juncos, PR seeks an experienced engineer to independently characterize and optimize processes within operations, manufacturing, pilot plant or capital projects. You will apply advanced engineering principles to design and implement major system modifications and analyze results for complex issues.

The role includes leading a small team, developing policies, and coordinating multi-disciplinary design and commissioning efforts for large-scale projects.

Qualifications

• Advanced knowledge of pharmaceutical/biotech processes.
• Experience with validation procedures (GLP/GMP).
• Ability to document in a highly regulated environment.
• Ability to supervise engineers and technicians.
• Strong problem-solving and analytical skills.

Responsibilities

• Develop and apply new engineering techniques and procedures.
• Lead design and implementation of major system modifications.
• Coordinate with R&D, manufacturing, facilities, QA and validation teams.
• Prepare budgets and project plans for large projects.
• Manage schedules and ensure timely delivery.

Skills

Pharma processes

GLPs/GMPs

Validation

Documentation

Lab equipment

Engineering science

Problem solving

Production engineering

Education

Doctorate or Masters + 2 years

Bachelors in Engineering + 4 years

Tools

Lab equipment

Validation docs software

Project management tools

Job description

Cis-International-LLC in Juncos, PR seeks an experienced engineer to independently characterize and optimize processes within operations, manufacturing, pilot plant or capital projects. You will apply advanced engineering principles to design and implement major system modifications and analyze results for complex issues.

The role includes leading a small team, developing policies, and coordinating multi-disciplinary design and commissioning efforts for large-scale projects.