Provide specialized automation and electrical/pneumatic design support to pharmaceutical projects, in accordance with process requirements and regulations, ensuring the technical quality of the systems as well as the achievement of the expected objectives.
We believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment.
Responsibilities
Perform the programming of process control systems installations together with the engineers responsible for each project.
Work with electrical resources to monitor the design, assembly, commissioning, and testing of automated systems.
Provide support during the qualification and validation phases of the systems.
Generate documentation at the level of algorithms, alarms, interlocks, and operator interfaces for the projects.
Explore new hardware solutions for automation, opening up new possibilities for future projects.
Develop internal automation procedures to increase the standardization of installations.
Supervise the work of external automation resources, ensuring the quality of work and compliance with project requirements.
Propose the most suitable software/hardware solution for each project to achieve the project objectives.
Assist, together with the project engineer, in defining the control strategy with the client.
Qualifications
Bachelor's degree in Electrical Engineering, Electronic Engineering, Automation/Control Engineering, or a related field.
Hands‐on experience with Siemens PCS 7, SIMATIC PCS neo, and Rockwell PlantPAx systems.
Proficient in PLC programming (S7‐1200/1500, ControlLogix) and HMI/SCADA development (WinCC, FactoryTalk).
Strong knowledge of batch control (ISA‐88), including recipe design, phases, operations, and procedure implementation.
Experienced in designing and maintaining distributed control architectures, including redundancy, segmentation, and cybersecurity considerations.
Able to integrate DCS/PLC systems with MES and ERP platforms and support computer system validation (CSV, IQ/OQ/PQ).
Comfortable working in regulated industries such as pharmaceutical, chemical, and food, ensuring compliance with GMP and industry standards.
Ability to communicate fluently in English (both written and spoken).
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Benefits
Contract of Employment: Permanent position
Schedule
Flexibility for U Program: Hybrid Model
Flexible schedule: Monday‐Thursday 7‐10 to 16‐19h and Friday 8‐15h (with the same flexible start time).
LocationParets del Vallès, Spain.
Grifols is an equal opportunity employer.
#J-18808-Ljbffr