Control & Instrumentation Engineer

SRG

Ribble Valley

On-site

GBP 60,000 - 80,000

Full time

14 days+

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Job summary

SRG is seeking a Control & Instrumentation Engineer to support delivery of systems across life science projects. Location: Manchester or Birmingham (3 Days On-Site). Contract Length: 6 Months.

Start Date: ASAP. You will provide technical leadership across automation, process control, and instrumentation disciplines while guiding engineering teams to successful delivery. The role requires experience with pharmaceutical/life sciences projects, DCS/PLC/SCADA, process instrumentation, and the

Qualifications

  • Experience in pharmaceutical, biopharmaceutical, or life sciences projects.
  • Extensive knowledge of DCS, PLC, and SCADA control systems.
  • Experience with process instrumentation and control systems.
  • Ability to produce and review engineering documentation including P&IDs and specifications.
  • Understanding of cGMP, GAMP, and ISA standards.

Responsibilities

  • Provide technical leadership across automation, process control, and instrumentation disciplines on life science projects.
  • Support engineering teams to ensure delivery of complex projects.

Skills

DCS
PLC
SCADA
Process instrumentation
P&IDs
Specifications
cGMP
GAMP
ISA standards

Job description

Job Title: Control & Instrumentation Engineer

Location: Manchester or Birmingham (3 Days On-Site)

Contract Length: 6 Months

Determination: Outside IR35

Start Date: ASAP

We're recruiting a Control & Instrumentation to support delivery of systems across a range of life science projects.

This role will provide technical leadership across automation, process control, and instrumentation disciplines while supporting engineering teams and ensuring the successful delivery of complex projects

Requirements:
  • Experience within pharmaceutical, biopharmaceutical, or life sciences projects.
  • Extensive knowledge of DCS, PLC, and SCADA control systems.
  • Experience with process instrumentation and control systems.
  • Ability to produce and review engineering documentation including P&IDs and specifications.
  • Understanding of cGMP, GAMP, and ISA standards.
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