About The Role
We are seeking a highly skilled Control Systems Engineer with a strong background in automation to join our MedTech engineering team.
The successful candidate will be responsible for designing, developing, validating, and maintaining control systems and automated solutions that support the manufacture of medical devices in compliance with regulatory standards (FDA, ISO *****, GMP).
Key Responsibilities
Design, implement, and maintain PLC-based control systems for automated manufacturing processes.
Collaborate with cross-functional teams (Manufacturing, Quality, R&D, Validation) to deliver robust and compliant automation solutions.
Develop and optimize automation strategies to improve efficiency, quality, and safety in medical device production.
Ensure systems comply with GAMP 5, FDA, ISO *****, and other relevant regulatory requirements.
Troubleshoot and resolve issues with automation systems, instrumentation, and process equipment.
Author and review technical documentation including URS, FDS, FAT, SAT, IQ, OQ, PQ protocols.
Provide technical support for validation, commissioning, and qualification of equipment and control systems.
Implement cybersecurity best practices for control and automation systems.
Train and mentor junior engineers or technicians on control systems and automation tools.
Key Skills & Experience
Bachelor's or Master's degree in Electrical Engineering, Control Systems, Automation, or related discipline.
Proven experience 5+ Yrs as a Control Systems Engineer / Automation Engineer in the MedTech, Pharma, or regulated manufacturing environment.
Strong knowledge of PLC programming (Siemens, Allen Bradley, Beckhoff, etc.), HMI, and SCADA systems.
Hands-on experience with industrial networks (Ethernet/IP, Profibus, Modbus) and instrumentation.
Familiarity with safety systems, LOTO procedures, and machine safety standards (ISO *****, IEC *****).
Knowledge of validation processes (IQ, OQ, PQ) in regulated industries.
Strong problem-solving and analytical skills.
Ability to work in a regulated environment with a strong focus on compliance and documentation.
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