Pharma Automation Engineer - CQV/Startup Specialist

NeoDyne

Dublin

On-site

EUR 50,000 - 70,000

Full time

14 days+

Application generator

An application made for this job — a tailored resume and cover letter that speak straight to the posting.

Get past ATS filters

Benefits offered by this job

Paid overtime

Flexible working hours

Opportunity to work on high-profile projects

Job summary

NeoDyne is seeking an Automation Engineer in Dublin to support automation projects for a pharmaceutical manufacturing facility. This role involves executing commissioning activities and ensuring compliance with GMP standards. Candidates must have a degree in Automation or Engineering and experience with automation project delivery.

The successful applicant will work closely with OEM suppliers and multidisciplinary teams, contributing to innovative automation solutions. Competitive hourly rate and flexible hours are offered.

Qualifications

Proven experience in automation projects within GMP-regulated environments.
Strong commissioning and start-up experience with manufacturing systems.
Understanding of CQV methodologies and validation lifecycle.

Responsibilities

Support delivery of automation systems for new pharmaceutical equipment.
Work with OEM vendors on installation and commissioning.
Execute commissioning according to project schedules.
Ensure compliance with GMP and site change control procedures.

Skills

Automation project execution

Troubleshooting

GMP compliance

Project collaboration

Education

Degree in Automation, Electrical Engineering, Mechatronics

Tools

Rockwell Automation (ControlLogix, FactoryTalk)

Job description

The successful applicant will work closely with OEM suppliers and multidisciplinary teams, contributing to innovative automation solutions. Competitive hourly rate and flexible hours are offered.

Get your free, confidential resume review.

or drag and drop your file here.