Why SimoTech
What is it like to work at SimoTech? With a
strong collaborative teamwork culture based on respect, trust and excellence,
we play a critical partnering role to our clients' life -changing supply of
products to patients. In return, there is excellent salary, benefits, career
progression, educational support and much more.
DeltaV Project Engineer 1629
SimoTech have an opportunity for a DeltaV
Project Engineer to join our team, supporting our client on their
state -of -the -art biotechnology manufacturing site in Dublin. The role sits on
the NPI (New Product Introduction) team and reports to the Automation Lead. The
successful candidate will work as part of the core engineering team, supporting
multiple key projects.
The ideal candidate will have 5+ years'
experience as an Automation Engineer in the life sciences industry, working
with Emerson DeltaV and/or PLC/SCADA systems.
Key
Responsibilities
1. Be a key
member of the NPI site project team, contributing to multiple projects.
2. Coordinate
with Process SMEs, CQV Leads, and Automation Engineers to understand process
requirements.
3. Liaise
with all relevant stakeholders to gather all key technical inputs for
Functional Design Specifications (FDS).
4. Provide
input, review and sign off on functional design aspects, as and when required.
5. Implement
ACPs (Automation Change Pack) to enable the required code changes.
6. Participate
in internal project reviews with key stakeholders within automation and with customers.
Requirements
7. Bachelor's
Degree in Engineering, Sciences or equivalent.
8. 5+
years of working experience as an Automation Engineer in a highly regulated
biotechnology environment.
9. 5
years' experience with DeltaV batch automation and/or PLC/SCADA systems, with
knowledge of the integration between DeltaV and PLC/SCADA systems desirable.
10. Ability
to interact and communicate with other engineering and business disciplines,
including Process Engineers, to define project scopes and deliver on project specifications.
11. Knowledge
of automation compliance lifecycle and change management.
12. Prior
process plant commissioning experience.
13. Good
understanding of life sciences regulations and compliance requirements including
GAMP, 21 CFR Part 11 and the S -88 Batch Standard is a must.
14. Strong
interpersonal and communication skills are required, with a proven ability to
communicate and build relationships cross -functionally.
15. Good
teamwork skills.
Benefits
16. Role provides a high degree of autonomy to allow the successful
candidate to reach their full potential.
17. Develop new skills and enhance technical ability by working with
innovative technologies in a multi -disciplined environment.
18. Opportunity to work with large corporate clients on exciting capital
projects.