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. Skellig is seeking a Senior MES Engineer with Syncade and cGMP experience to support our clients across North America. To be considered for this role you must have Syncade experience and experience working in biotech/pharma. Our projects are based at our client’s facilities. Generally, at a large biotech manufacturing facility with a dedicated Syncade 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. 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. From its inception, Skellig has strived to be ‘more human.’ We work hard to foster a culture that promotes innovation, diversity, and great work. A culture that rewards problem solving, teamwork, and service excellence. And one that attracts the top talent and premier clients. Ours is a culture of honesty, transparency, and kindness — A people-focused and compassionate company.
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Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
Number of Employees
101-250 employees