skellig
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. Overview
Specialist providers of pharmaceutical automation, process and project controls. Skellig was founded to radically improve upon the way automation, process, and project controls are provided. It’s a goal that is grounded in efficiency, transparency, and our client’s total peace of mind — this is the vision behind everything we do. Responsibilities
Design, code, implement, and test changes for new and existing equipment on the client’s DeltaV system. Author, develop and execute validation test plans. 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. Qualifications
Minimum of 3 years Automation Experience, preferably with DeltaV Prior Pharmaceutical Industry Experience Benefits
Vacation / Personal Paid Time Off Sick Paid Time Off Paid Public Holidays Parental Leave Health, Dental, and Vision PPO Insurance for you and dependents – premiums are 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 large biotech manufacturing facilities with a dedicated DeltaV system. Engineers are required to be onsite at least 2-3 days a week, depending on the client’s requirements. As with all our team members, you’ll be supported with back-up and resources you need. Equal Employment Opportunity
Skellig is an equal opportunity employer. We do not discriminate on the basis of any protected status under applicable law.
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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. Overview
Specialist providers of pharmaceutical automation, process and project controls. Skellig was founded to radically improve upon the way automation, process, and project controls are provided. It’s a goal that is grounded in efficiency, transparency, and our client’s total peace of mind — this is the vision behind everything we do. Responsibilities
Design, code, implement, and test changes for new and existing equipment on the client’s DeltaV system. Author, develop and execute validation test plans. 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. Qualifications
Minimum of 3 years Automation Experience, preferably with DeltaV Prior Pharmaceutical Industry Experience Benefits
Vacation / Personal Paid Time Off Sick Paid Time Off Paid Public Holidays Parental Leave Health, Dental, and Vision PPO Insurance for you and dependents – premiums are 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 large biotech manufacturing facilities with a dedicated DeltaV system. Engineers are required to be onsite at least 2-3 days a week, depending on the client’s requirements. As with all our team members, you’ll be supported with back-up and resources you need. Equal Employment Opportunity
Skellig is an equal opportunity employer. We do not discriminate on the basis of any protected status under applicable law.
#J-18808-Ljbffr