VEQTOR
Lead Automation Controls Engineer -DeltaV
VEQTOR, San Diego, California, United States, 92189
VEQTOR is seeking an experienced Lead Automation Controls Engineer with a strong background in DCS DeltaV. This is a highly visible, hands‑on role with direct impact on commercial biopharmaceutical manufacturing systems. You will own DeltaV configuration, troubleshooting, and lifecycle management for chromatography and downstream purification skids in a GxP environment, while collaborating with global validation, QA, and process teams.
Responsibilities
Configure, troubleshoot and maintain DeltaV Batch (recipes, phases, equipment modules, class‑based recipes)
Support software and infrastructure upgrades within regulated environments.
Have a strong GDP and Quality background.
Author, review, and update GMP lifecycle documentation (URS, FS, DS, etc.).
Develop and execute FAT/SAT/CMG protocols.
Perform data integrity (ALCOA+) assessments and 21 CFR Part 11 remediation
Support control system infrastructure for both VEQTOR and client systems
Collaborate with global teams to deliver automation projects efficiently
Qualifications / Requirements
Bachelor’s degree in Engineering, Computer Science, or equivalent experience
Direct experience and knowledge of DeltaV (min 4 years) in a regulated environment
Experience with CSV processes, GMP documentation, and regulatory requirements
Must be able to work 100% on-site in Southern California
Prior experience in the pharmaceutical or biotechnology industry (required).
Excellent technical writing, organizational, and communication skills
Ideal Candidate Attributes
Detail oriented, self‑motivated and a team player
Ability to work in a fast‑paced, high‑energy environment
Ability to perform critical analysis of situations and provide recommendations
Problem solving, creative thinking, and interaction with upper management and design teams
Ability to work independently with structured guidance
Ability to uphold VEQTOR values and demonstrate honesty, integrity, pride, accountability, teamwork, and commitment
Seniority Level Mid‑Senior level
Employment type Full‑time
Job function Engineering and Information Technology
Industries Professional Services
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Responsibilities
Configure, troubleshoot and maintain DeltaV Batch (recipes, phases, equipment modules, class‑based recipes)
Support software and infrastructure upgrades within regulated environments.
Have a strong GDP and Quality background.
Author, review, and update GMP lifecycle documentation (URS, FS, DS, etc.).
Develop and execute FAT/SAT/CMG protocols.
Perform data integrity (ALCOA+) assessments and 21 CFR Part 11 remediation
Support control system infrastructure for both VEQTOR and client systems
Collaborate with global teams to deliver automation projects efficiently
Qualifications / Requirements
Bachelor’s degree in Engineering, Computer Science, or equivalent experience
Direct experience and knowledge of DeltaV (min 4 years) in a regulated environment
Experience with CSV processes, GMP documentation, and regulatory requirements
Must be able to work 100% on-site in Southern California
Prior experience in the pharmaceutical or biotechnology industry (required).
Excellent technical writing, organizational, and communication skills
Ideal Candidate Attributes
Detail oriented, self‑motivated and a team player
Ability to work in a fast‑paced, high‑energy environment
Ability to perform critical analysis of situations and provide recommendations
Problem solving, creative thinking, and interaction with upper management and design teams
Ability to work independently with structured guidance
Ability to uphold VEQTOR values and demonstrate honesty, integrity, pride, accountability, teamwork, and commitment
Seniority Level Mid‑Senior level
Employment type Full‑time
Job function Engineering and Information Technology
Industries Professional Services
#J-18808-Ljbffr