Sr. Controls Engineer Position Available In Sumter, South Carolina
Tallo's Job Summary: The Sr. Controls Engineer position involves supporting the startup of a production line, conducting testing, identifying malfunctions, ensuring safety standards, and optimizing equipment parameters. Key skills include PLC programming, troubleshooting, and Allen Bradley PLC knowledge. The role requires 7-10 years of experience, familiarity with medical device sector processes, and the ability to work onsite in Sumter, SC, with travel to Chicago, IL or Bristol, CT. Benefits include paid time off and holidays.
Job Description
Job Title:
Sr. Controls Engineer Job Description We are seeking an experienced Sr. Controls Engineer to support the startup of a new production line that was constructed a few years ago, temporarily mothballed, and is now being reactivated. This role involves ensuring the operational effectiveness and compliance of the production line while working closely with cross-functional teams. Responsibilities Conduct Factory Acceptance Tests (FAT) and Site Acceptance Tests (SAT). Identify and debug mechanical, electrical, or software malfunctions. Ensure that safety standards are met, including mechanical, electrical, and ergonomic considerations. Oversee the fine-tuning and debugging of program logic and user interfaces. Optimize equipment parameters to achieve the desired Overall Equipment Effectiveness (OEE). Utilize optical instruments for precise measurements or imaging, specifically Data Logic and Cognex vision systems. Collaborate with cross-functional teams to maintain records, generate reports, and ensure compliance. Essential Skills Proficiency in PLC programming and controls engineering. Experience with FAT/SAT processes, especially in the medical device sector. Strong troubleshooting and problem-solving skills. Knowledge of Allen Bradley PLC. High-speed machine automation experience. Additional Skills & Qualifications 7-10 years of experience in line commissioning controls engineering. Experience with SAT/FAT processes in a regulated manufacturing space, preferably within the medical device industry. Proficiency in basic office programs such as Word, Excel, and Project. Basic awareness of ISO standards. Ability to integrate with the client’s site engineering team and work under their direction. Work Environment The position is based onsite in Sumter, SC, with travel required to Chicago, IL or Bristol, CT for 3-4 weeks for site assessments. The role demands a great attitude, professionalism, and excellent communication skills, as you will be working closely with the client’s site engineering team, mechanical/electrical technicians, and operators. Benefits include 2 weeks of paid time off and 6 paid holidays.