Senior CSV Automation Engineer (Rockwell/PharmaSuite)

Trinity Consultants - Advent Engineering; Bend (OR); On-site; USD 120,000 - 180,000; Full time

Job summary

ADVENT Engineering seeks a Sr. Automation CSV Engineer to lead complex CSV and automation work for PCS/MES migrations at a regulated biotech/pharma site in the California Bay area, with 100% onsite in Bend, OR. Deep Rockwell and PharmaSuite experience is required.

You will validate, document, and collaborate with cross‑functional teams to ensure data integrity, SDLC adherence, and regulatory compliance across the project lifecycle.

Qualifications

• 8+ years of experience in CSV and Automation within a regulated biotech/pharma environment.
• Hands‑on experience with implementation, migration, and validation of PCS (Rockwell and/or Honeywell).
• Hands‑on experience with MES (PharmaSuite, POMSnet) and SCADA/PLC systems.
• Strong, hands‑on expertise with Rockwell and PharmaSuite (required).
• In‑depth knowledge of SDLC, 21 CFR Part 11 / Annex 11, Data Integrity, and CSV.

Responsibilities

• Lead and execute CSV and automation activities for PCS/MES system migration projects.
• Support implementation, migration, commissioning, and validation of PCS (Rockwell, Honeywell) and MES (PharmaSuite, POMSnet).
• Ensure compliance with SDLC, 21 CFR Part 11, Annex 11, Data Integrity, and GAMP 5.
• Manage and document software changes throughout the SDLC per site procedures.
• Support programming, configuration, commissioning, and validation of Rockwell and PharmaSuite platforms.
• Collaborate with automation, IT, QA, and manufacturing teams.
• Communicate effectively with stakeholders at all levels.

Skills

CSV

Automation

Rockwell

PharmaSuite

POMSnet

Data Integrity

SDLC

21 CFR Part 11

GAMP 5

Team Collaboration

Tools

Rockwell

PharmaSuite

POMSnet

FactoryTalk

Kneat

Job description

ADVENT Engineering seeks a Sr. Automation CSV Engineer to lead complex CSV and automation work for PCS/MES migrations at a regulated biotech/pharma site in the California Bay area, with 100% onsite in Bend, OR. Deep Rockwell and PharmaSuite experience is required.

You will validate, document, and collaborate with cross‑functional teams to ensure data integrity, SDLC adherence, and regulatory compliance across the project lifecycle.