Pharmaceutical Process Specialist

1 week ago


Birmingham, Birmingham, United Kingdom Integrated Project Services Full time
About the Job

We are seeking a Pharmaceutical Process Specialist to join our team at IPS. The successful candidate will have extensive experience in designing and implementing industrial control systems for pharmaceutical processes.

About the Team:

Our team at IPS is passionate about delivering world-class designs for our pharmaceutical clients. We are a caring and nimble team that takes pride in our work and strives to make a difference in the lives of people.

About the Role:

  • Develop automation User Requirements Specifications (URS) based on customer needs.
  • Actively collaborate with the process design and project teams to support the execution of successful project studies.
  • Develop the design and specifications for DCS, PLC, and SCADA-based process control systems for IPS clients and projects.
  • Collaborate with client counterparts to develop control systems concepts, architectures, and control platforms as applied to the client project.
  • Identify, qualify, and collaborate with third-party system integrators as necessary to support project and company business objectives.
  • Support business development for process automation design and implementation. Assist in proposals, estimates, presentations, and other sales and marketing documents.
  • Assist process engineering development of P&IDs and process control requirements, as well as Functional Requirement Specifications (FRS).
  • Work with end users and Original Equipment Manufacturers (OEMs) to coordinate the application of automation products.
  • Support risk assessments, including SIL, LOPA, and HAZOP.
  • Support IQ/OQ development and participate in systems analysis, validation, and verification.

Requirements:

  • Bachelor's degree in engineering or equivalent degree from an accredited university.
  • 10+ years of experience with industrial process control systems including DCS, PLC, and SCADA-based systems, of which ideally, 5 years of experience with pharmaceutical process instrumentation.
  • Expertise in computer operation for engineering design programs and computer-aided drafting.
  • Experience with the development of cGMP and GAMP automation lifecycle documents.
  • Excellent interpersonal skills and presence to deal effectively with senior-level contacts.


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