Role & seniority: Automation Engineer, mid-level (3–5 years’ pharmaceutical/regulated ops experience)

Stack/tools: DeltaV programming (batch processes), computer systems validation (CSV) in GMP/regulatory environments, change control, QA/QC documentation, MS Project, Excel; strong awareness of EHS standards

Top 3 responsibilities

Support 24/7 automation and control systems; troubleshoot and resolve issues
Develop, update, test control software/hardware; install/configure equipment with vendors; lead investigations and corrective actions
Create/manage change controls and CSV documentation; ensure compliance with policies, quality standards, and site initiatives

Must-have skills

DeltaV programming expertise (especially batch processes)
Experience with CSV in regulated environments
Bachelor’s degree in Electrical, Chemical, Computer, Mechanical, or Industrial Engineering; 3–5 years pharma Ops support
Strong problem-solving, communication, teamwork; ability to manage multiple projects; organized; fluent in English (and Spanish preferred)

Nice-to-haves

Leadership and cross-functional collaboration experience
Ability to thrive under uncertainty and pressure; accountable, result-driven
Proficiency with MS Project and Excel; ability to drive site initiatives
Location & work type: Puerto Rico office; on-site with requirement to support a 24/7 operation

Full Description

PACIV, a global leader in industrial automation solutions servicing the Life Sciences sector, is looking for a Automation Engineer for its Puerto Rico office.

Position Responsibilities/Essential Functions

Support automation and control systems for 24/7 operations.
Develop, update, and test control system software and hardware.
Install and coordinate automation equipment and software, including working with vendors.
Troubleshoot control system issues and implement solutions.
Provide technical support to automation technicians.
Identify customer needs and address concerns about control systems.
Monitor system performance, analyze trends, and define action plans.
Evaluate automation systems to prevent safety, quality, or downtime risks.
Lead investigations and implement corrective actions.
Create and manage change controls, including technical assessments and cost estimates.
Develop, review, and approve CSV documentation.
Ensure validation and compliance with policies, quality standards, and EHS regulations.
Communicate activities, priorities, and updates to teams and stakeholders.
Participate in meetings and help drive key site initiatives.
Understand how process, equipment, and control system changes affect automation.

Requirements

Bachelor’s degree in engineering (Electrical, Chemical, Computer, Mechanical, or Industrial).
3–5 years supporting pharmaceutical operations
Availability to support a 24/7 operation.

Desired Hard Skill Sets

Strong DeltaV programming skills (especially batch processes).
Experience with computer systems validation (CSV) in regulated/GMP environments.

Desired Soft Skills

Strong problem-solving, communication, leadership, and teamwork skills.
Ability to manage multiple projects and adapt quickly.
Deals well with uncertainty and pressure.
Works well with others, within a team and takes accountability.
Result driven and self-motivated.
Organized, with strong computer literacy such as MS Project, Excel, etc.
Fully fluent in English and Spanish.