Responsibilities
· Provide day-to-day automation and controls
support for plasmid manufacturing processes and plant operations.
· Troubleshoot automation, control systems, PLCs,
HMIs, instrumentation, and related manufacturing equipment.
· Support the maintenance, modification, and
optimization of automation systems to improve equipment reliability and
production efficiency.
· Assist with the development, testing,
implementation, and documentation of automation system changes.
· Participate in equipment commissioning,
qualification, startup, and troubleshooting activities.
· Work with Manufacturing and Maintenance teams to
identify automation-related issues and implement effective corrective actions.
· Support plant control systems, process
equipment, utilities, and facility automation as needed.
· Assist with system upgrades, software changes,
alarm management, and control strategy improvements.
· Maintain accurate technical documentation,
including automation specifications, system documentation, change controls, and
troubleshooting records.
· Support investigations, deviations, CAPAs, and
other quality-related activities associated with automation systems.
· Ensure automation activities comply with
applicable GMP, safety, quality, and regulatory requirements.
· Collaborate with cross-functional teams and
external vendors/contractors on automation projects and technical issues.
· Participate in on-call or off-hours support
activities when required to maintain plant operations.
· Bachelor's degree in Electrical Engineering,
Automation Engineering, Controls Engineering, Computer Engineering, or a
related technical field; equivalent experience may be considered.
· 2–5 years of experience in automation,
controls, instrumentation, or manufacturing engineering.
· Experience working with PLC and HMI
systems, industrial control systems, or manufacturing automation.
· Ability to troubleshoot electrical, controls,
instrumentation, and automation-related issues.
· Experience supporting manufacturing or plant
operations in a pharmaceutical, biotechnology, chemical, or other
regulated environment is preferred.
· Familiarity with GMP, GxP, FDA-regulated
environments, or computerized system validation is a plus.
· Experience with automation system documentation,
change controls, testing, commissioning, or qualification is preferred.
· Strong analytical and problem-solving skills
with the ability to respond effectively to equipment and production issues.
· Ability to work collaboratively with
Manufacturing, Engineering, Maintenance, Quality, and other technical teams.
· Strong written and verbal communication skills.
· Ability to manage multiple priorities in a
fast-paced manufacturing environment.
· Willingness to provide occasional off-hours or
on-call support when required.
| Location | Baltimore, Maryland |
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