Automation Engineer

We are seeking an experienced Automation Engineer to support automation, controls, instrumentation, and manufacturing systems within a GMP biopharmaceutical manufacturing environment. This role will work closely with Engineering, Manufacturing, Facilities, Validation, Quality, and external vendors to maintain, troubleshoot, improve, and implement automation systems supporting manufacturing operations. The ideal candidate brings hands-on experience with industrial automation and controls in a regulated pharmaceutical, biotechnology, or other GMP manufacturing environment, along with a strong understanding of equipment, instrumentation, process control, and computerized systems. ResponsibilitiesProvide day-to-day engineering support for manufacturing automation, control systems, instrumentation, and automated equipmentTroubleshoot and resolve issues involving PLCs, HMIs, SCADA systems, instrumentation, electrical controls, and associated automation hardware/softwareSupport commissioning, qualification, startup, and implementation of new and modified manufacturing equipment and systemsPartner with Validation and Quality to ensure automation and computerized systems remain in a compliant, validated stateDevelop, review, and execute automation-related documentation, including requirements, specifications, test protocols, and technical reportsSupport change controls, deviations, CAPAs, investigations, and continuous improvement initiativesWork with equipment manufacturers, system integrators, and other external vendors on automation projects and troubleshootingSupport upgrades, modifications, and lifecycle management of automation and control systemsCollaborate cross-functionally with Manufacturing, MSAT, Process Engineering, Facilities, Validation, and Quality teamsParticipate in equipment and system risk assessments and identify opportunities to improve reliability, efficiency, and process controlMaintain appropriate technical documentation, system records, and SOPs in accordance with GMP requirementsProvide technical support during manufacturing campaigns and help minimize equipment and automation-related downtime QualificationsBachelor's degree in Electrical Engineering, Automation Engineering, Controls Engineering, Chemical Engineering, Mechanical Engineering, or a related technical discipline5+ years of experience in automation, controls, instrumentation, or manufacturing engineering, preferably within pharmaceutical, biotechnology, cell & gene therapy, or another GMP-regulated environmentHands-on experience with PLC-based control systems, HMIs, SCADA, and industrial automationStrong understanding of instrumentation, process controls, electrical systems, motors, drives, and automated manufacturing equipmentExperience supporting GMP manufacturing equipment and/or facility systemsExperience with commissioning, qualification, validation, or implementation of automated systemsWorking knowledge of GMP requirements and regulated change-control/documentation practicesExperience troubleshooting complex automation and equipment issues in a manufacturing environmentStrong communication and cross-functional collaboration skillsAbility to manage multiple priorities and work effectively in a fast-paced manufacturing environment Preferred QualificationsExperience in a biopharmaceutical manufacturing facilityExperience with PLC platforms such as Allen-Bradley/Rockwell or similar systemsExperience with SCADA/HMI platforms and industrial communication protocolsExperience with DeltaV or other DCS platformsExperience with computerized system validation (CSV) or automation system validationExperience supporting facility/utilities automationExperience working with system integrators and automation vendorsExperience with biologics, cell therapy, gene therapy, viral vector, or other advanced manufacturing processesLocation: Framingham, MA Employment Type: Contract Ideal Candidate Profile The ideal candidate is a hands-on automation/controls engineer who is comfortable working directly with manufacturing teams and troubleshooting issues on the floor, while also being able to operate within a highly regulated GMP environment. They should be equally comfortable working on PLC/controls issues, instrumentation and equipment troubleshooting, validation documentation, and cross-functional engineering projects. Disclosure: The hourly rates and/or salaries listed may or may not reflect total compensation packages including bonus and fringe benefits, etc., nor are the advertisement(s) posted a guarantee of a certain compensation package for a position or bona fide offer of employment. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.