Senior Process Engineer — Pharma/Biotech Design & Validation

CIS International LLC; Juncos (PR); On-site; USD 85,000 - 120,000; Full time

Job summary

CIS International LLC in Juncos, PR, is seeking an experienced engineering professional to lead process optimization and capital projects in a highly regulated environment. You will design major system modifications, supervise staff, and collaborate with diverse departments to translate complex requirements into actionable plans.

The role emphasizes applying mature engineering knowledge to project planning, validation, and production support, with a strong preference for pharma/medical device

Qualifications

• Demonstrated experience applying advanced engineering principles to complex projects.
• Experience in medical device or pharma environments preferred.
• Ability to lead and mentor a small team of engineers and technicians.

Responsibilities

• Develop and apply engineering techniques for major system modifications.
• Direct and review work of engineers and technicians on projects.
• Coordinate with research, manufacturing, utilities, QA and validation teams.
• Work with project managers to meet schedule, budget and quality constraints.
• Develop budgets for multi-discipline projects and manage contractors.

Skills

Pharmaceutical/biotech processes

Validation processes

Documentation in regulated env

GLPs and GMPs

Engineering problem solving

Project management

Leadership/teambuilding

Packaging equipment knowledge

Design of new equipment processes

Engineering project management

Validation experience in regulated env

Education

Doctorate or Masters + 2 years of Engineering experience

Bachelors in Engineering + 4 years of Engineering experience

Bachelor's degree in Engineering and 5 years of Engineering experience

Job description

CIS International LLC in Juncos, PR, is seeking an experienced engineering professional to lead process optimization and capital projects in a highly regulated environment. You will design major system modifications, supervise staff, and collaborate with diverse departments to translate complex requirements into actionable plans.

The role emphasizes applying mature engineering knowledge to project planning, validation, and production support, with a strong preference for pharma/medical device