Automation Area Lead – DeltaV

Automation Area Lead – DeltaV

Position Title & Basic Details

We're looking for an Automation Area Lead based in Indianapolis, IN. This is a full-time position requiring 8+ years of relevant experience. A Bachelors degree in Engineering is strongly preferred.

Overview

In this role, you'll be responsible for the control system solution for an area within a project, ensuring alignment with the overall program automation philosophy, standards, and user requirements. The ideal candidate brings a solid foundation in DeltaV Batch DCS and thrives in a collaborative environment.

Key Responsibilities

- Take technical ownership for an area within a project.

- Define the S88 software structure and list for the designated area.

- Develop draft functional design specifications and collaborate with system integrators to finalize them.

- Participate in P&ID and control strategy reviews.

- Work closely with the Project Technical Lead and System Integrator to deliver the project on schedule and budget.

- Collaborate with Program technical offices for consistent automation deliverables.

- Assist in defining software components for creation or modification.

- Communicate progress, issues, and needs to the automation technical lead.

- Develop Parameter and Recipe Specification documents.

- Respond to system integrator technical queries and identify remediation efforts for process control software.

- Manage issue tracking and analyze technical risks related to the area.

- Ensure compliance with training requirements.

Requirements

Education: Bachelors degree in Engineering or equivalent experience.

Technical Expertise: Proficiency in DeltaV Batch DCS; familiarity with Allen-Bradley PLCs is a plus.

Experience: Minimum 8 years of working automation experience in the pharmaceutical industry, preferably in API/bulk manufacturing.

Soft Skills: Excellent written and verbal communication skills for both technical and non-technical audiences and exceptional teamwork abilities.

Preferred Qualifications

Previous experience with large pharmaceutical automation projects.

Strong knowledge of GMPs, regulatory requirements, and computer system validation principles.

Why Join Us?

Growth Opportunities: Work with a team that will enhance your technical development.

Innovative Environment: Engage with cutting-edge technologies and challenging projects."