Automation Engineer (pharmaceutical Manufacturing)

Skellig is seeking an Automation Engineer with DeltaV and cGMP experience to support our clients across North America. To be considered for this role you must have DeltaV experience and experience working in biotech/pharma.

REQUIREMENTS:

• A minimum of 3 years Automation Experience Preferably with DeltaV
• Prior Pharmaceutical Industry Experience
  
  BENEFITS:

Here's what's waiting for you as one of our Automation Engineers
• Vacation / Personal Paid Time Off
• Sick Paid Time Off
• Paid Public Holidays
• Parental Leave
• Full Heath, Dental, and Vision PPO Insurance for you and any dependents - Premiums are 100% fully covered
• Life Insurance and Accidental Death and Dismemberment
• 401k
• Education Reimbursement
• Relocation package

PROJECT OVERVIEW:
Our projects are based at our client’s facilities.  Generally, at a large biotech manufacturing facility with a dedicated DeltaV system. Unless otherwise noted in the job posting, engineers are required to be onsite at least 2-3 days a week, sometimes more depending on the client’s requirements.

Your job will be to follow all client procedures to independently:
1. Design, code, implement, and test changes for new and existing equipment on the client’s DeltaV system.
3. Author, develop and execute validation test plans.
4. Support general project activities which include, but are not limited to, participating in client meetings, escalating project issues to the appropriate client staff, working with the client’s vendors, attending all required client training, and engaging with the client’s supporting teams.

It's important to be respectful, compassionate, a good communicator, and well organized.

As with all our team members, you'll be extremely well looked after. We'll make sure you receive all the back-up and support you need.