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Senior s7 automation engineer

Dublin
Impact Iel
Automation engineer
Posted: 24 December
Offer description

Technical Recruiter - Impact Engineering
Role Overview
Impact Engineering is partnering with a leading global pharmaceutical manufacturing organisation, to hire a
Senior Siemens S7 Automation Engineer
.
The successful candidate will join the
MSA team
and take technical ownership of the
PLC layer across multiple site-wide automation upgrade projects
.
This role will focus primarily on
Siemens S7 PLC systems
, including
legacy to modern platform upgrades
, while interfacing with
DeltaV DCS systems
and a wide range of pharmaceutical manufacturing equipment.
This is a
senior, hands-on engineering role
requiring strong technical leadership, structured execution, and experience working in
regulated GMP environments
.
Key Responsibilities
Lead the
PLC scope
for multiple automation upgrade projects within a
live pharmaceutical manufacturing environment
Deliver
Siemens S7 PLC upgrades
, including
S***** to S****** migrations
Perform PLC
software design, development, testing, and commissioning
Support and implement
PLC–DCS interfaces
, including integration with
Emerson DeltaV
Work with a wide range of
OEM and vendor equipment
(process skids, utilities, packaging, and ancillary systems)
Participate in
FAT, SAT, and commissioning activities
Ensure all automation activities comply with
GMP, GAMP 5, and site quality standards
Support
change management, system lifecycle documentation, and validation deliverables
Collaborate with cross-functional teams including
MSA, Validation, Engineering, IT, and Operations
Act as a
technical reference point
for Siemens PLC systems on site
Required Experience & Skills
Degree in
Automation, Electrical, Electronic, or Software Engineering
(or equivalent experience)
Strong hands-on experience with
Siemens S7 PLC platforms
S*****, S*****, and S******
TIA Portal
Proven experience delivering
PLC upgrade projects
in an industrial environment
Prior exposure to
S***** ? S****** migrations
is highly desirable
Experience working in
pharmaceutical or biotech manufacturing environments
Familiarity with
DeltaV interfaces
or DCS integration is a strong advantage
Understanding of
GMP, GAMP 5, and regulated system lifecycle requirements
Experience with
FAT/SAT, commissioning, and troubleshooting
Strong documentation, communication, and stakeholder engagement skills
Ability to work independently while leading technical scopes within a project team
#J-*****-Ljbffr

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