Key Responsibilities
* Coordinate the development of automation
software and hardware
to meet New Product Introduction schedules, including
FATs, SATs, commissioning, and validation
.
* Develop and implement automation solutions in line with
S88 batch process standards
.
* Deliver
robust, compliant, and cost-effective automation solutions
within agreed timelines for capital projects.
* Support the
Commissioning, Qualification, and Validation (CQV) teams
during DeltaV software shakedown and verification.
* Design, code, and test
DeltaV software changes
identified during commissioning.
* Collaborate closely with other Automation Engineers to ensure milestones are met and
standards/library modules
are consistently applied.
Qualifications & Requirements
* Minimum
3 years' DeltaV experience
on-site in a pharmaceutical environment.
* Strong experience designing and programming
control systems
with emphasis on DeltaV DCS.
* Knowledge of
S88 batch process control
in the (Bio)Pharma sector.
* Ability to troubleshoot
hardware configurations, operator interfaces, and databases
.
* Familiarity with
GMP standards
; knowledge of
21 CFR Part 11
is a plus.
* Experience in
commissioning and start-up
of control systems.
* Strong
interpersonal and teamwork skills
.
* Ability to work effectively in
fast-paced, project-driven environments
.
* Experience with
PLC, HMI, SCADA, and process instrumentation
is advantageous.
INDFRS2