Control Systems Developer

7 days ago

Swindon, Swindon, United Kingdom RBW Consulting Full time

**Job Summary**

RBW Consulting is seeking an experienced Automation Controls Specialist to join our team. As an Automation Controls Specialist, you will be responsible for designing, developing, and implementing control systems and automation solutions for pharmaceutical manufacturing processes.

Key Responsibilities:

  • Design and implement control systems and automation solutions for pharmaceutical manufacturing processes.
  • Develop and maintain automation standards and documentation.
  • Troubleshoot and resolve control system and automation equipment issues.
  • Ensure compliance with cGMP and safety standards.
  • Collaborate with cross-functional teams for process optimization.
  • Provide technical support for automation equipment and software.
  • Create maintenance plans for manufacturing and packing equipment software.
  • Perform system upgrades and modifications.
  • Stay updated on automation technology and industry regulations.
  • Share expertise with colleagues to improve understanding and performance.
  • Create and implement task instructions for Controls and Automation tasks.
  • Participate in the design and commissioning of new production facilities and equipment.
  • Ensure program data security in accordance with Computer System Validation (CSV) requirements.
  • Maintain a database of optimal program settings for equipment recovery.
  • Design and write PLC, HMI, and SCADA control system software.
  • Work with third-party specialists to implement best practices for machine software.
  • Develop and execute validation protocols for control systems and automation equipment.

Qualifications:

  • Experience with proactive maintenance approaches such as CBM, PPM, and OAC.
  • Proficient in troubleshooting and resolving control and automation systems issues.
  • Knowledge of PLC/HMI systems like Siemens, Allen Bradley, or Mitsubishi.
  • Demonstrated experience in leading continuous improvement activities.
  • Background in pharmaceutical or Biotech environments.
  • Strong knowledge of Health and Safety Compliance.
  • Effective time management and workload organization.
  • Excellent communication skills with stakeholders at all levels.
  • Experience in GMP-regulated manufacturing environments.
  • Ability to amend and improve process controls.
  • Proven track record in driving continuous improvement projects.

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