Automation Systems Expert

Location

• Automation Systems

  : Proficiency in designing and implementing automation solutions, including programmable logic controllers (PLCs), distributed control systems (DCS), and supervisory control and data acquisition (SCADA) systems.

• Control Systems

  : Knowledge of process control principles, including PID (Proportional- Integral-Derivative) controllers, feedback loops, and real-time monitoring. Robotics and Instrumentation: Experience with robotic systems, sensors, actuators, and other instrumentation used in bioprocess automation (e.g., bioreactors, fermenters).

• Bioprocess knowledge

  : Understanding of bioprocessing techniques such as fermentation, cell culture, downstream processing (e.g., purification, filtration), and scale-up from lab to production.Familiarity with biological systems, including microbial and mammalian cell cultures, and their integration with automated workflows.
• Knowledge of Good Manufacturing Practices (GMP) and regulatory standards (e.g., FDA, EMA) relevant to bioprocess environments

• Technology Selection

  : Research and recommend automation technologies tailored to biotechnology and medical product development needs.

• Cross-Functional Collaboration

  : Partner with R&D, quality assurance, and regulatory teams to align automation efforts with project timelines, quality standards, and compliance needs.

• Regulatory Compliance

  : Ensure automated systems adhere to healthcare and pharmaceutical standards (e.g., GMP, FDA 21 CFR Part 11), supporting validation and documentation efforts.

• Training & Support

  : Train team members on automation tools and foster their adoption to enhance productivity across the product development lifecycle.

• Proficiency in programming languages such as Python, C++, or Java for developing automation scripts and control algorithms.
• Experience with software platforms like LabVIEW, MATLAB, or similar tools for simulation, data analysis, and system modeling.
• Experience with automation software (e.g., Siemens PCS 7, Rockwell Automation, DeltaV, etc.)
• Understanding of product development cycles in regulated environments, such as medical devices, diagnostics, or drug formulation.

• Strong problem-solving skills with an emphasis on process improvement.
• Hands-on experience designing and maintaining automated systems.
• Ability to work effectively in multidisciplinary teams with scientific and regulatory stakeholders.
• Excellent communication and documentation skills.

• Experience with biotechnology/medical-specific automation, such as bioreactor control unit design.
• Familiarity with regulatory standards (e.g., FDA, EMA) and quality systems (e.g., ISO 13485, GxP).

• Innovative thinking with a practical focus
• Precision and attention to regulatory detail
• Adaptability in a fast-evolving industry