skellig
Overview
Skellig is a specialist provider of pharmaceutical automation, process and project controls. Skellig was founded to radically improve automation, process, and project controls with a focus on efficiency, transparency, and client peace of mind. Skellig is seeking a Senior MES Engineer with PAS-X and cGMP experience to support our clients across North America. To be considered for this role you must have PAS-X experience and experience working in biotech/pharma. Responsibilities
Lead small to large teams (depending on experience) to complete automation projects to fulfill client needs. Design, configure, implement, and test changes for new and existing Recipes, eLogs, Workflows, Work Instructions, Integrations, and system integration solutions on the client’s PAS-X system. Author, develop and execute validation test plans. Create basic project schedules that communicate progress and milestones. Support general project activities, including participating in client meetings, escalating issues, coordinating with the client’s vendors, and engaging with client support teams. Adhere to client procedures and maintain professional, respectful, and organized communication. Qualifications
Minimum of 2 years MES experience, preferably with PAS-X. Prior pharmaceutical industry experience. Experience working in biotech/pharma and with PAS-X is required. Project & Onsite Details
Projects are located at client facilities, typically large biotech manufacturing facilities with a dedicated PAS-X system. Engineers are required to be onsite at least 2–3 days a week, depending on client requirements. Benefits
Vacation / Personal Paid Time Off Sick Paid Time Off Paid Public Holidays Parental Leave Sabbatical Full health, dental, and vision PPO insurance for you and dependents (premiums fully covered) Life Insurance and Accidental Death and Dismemberment 401(k) Education Reimbursement Relocation package Company Culture
From its inception, Skellig has strived to be ‘more human.’ We foster a culture that promotes innovation, diversity, and great work, rewarding problem solving, teamwork, and service excellence. Our culture emphasizes honesty, transparency, and kindness—people-focused and compassionate. Application
Interested in building your career at Skellig? Apply through the form below to get future opportunities sent to your email. Apply for this job * indicates a required field First Name * Last Name * Email * Phone Country * Phone * Resume/CV * Enter manually Accepted file types: pdf, doc, docx, txt, rtf Education Degree LinkedIn Profile Website Voluntary Self-Identification
For government reporting purposes, we ask candidates to respond to the below self-identification survey. Completion of the form is voluntary and will not affect hiring decisions. Any information provided will be kept confidential. As part of Skellig’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected status under applicable law. This section describes categories of protected veterans and disability status to support our compliance with VEVRAA and OFCCP. Voluntary Self-Identification of Disability Form CC-305 OMB Control Number 1250-0005 (Expires 04/30/2026) Why are you being asked to complete this form? We are a federal contractor or subcontractor and must measure our progress toward a goal of having workers with disabilities. Completion is voluntary and confidential. For more information, visit the OFCCP website.
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Skellig is a specialist provider of pharmaceutical automation, process and project controls. Skellig was founded to radically improve automation, process, and project controls with a focus on efficiency, transparency, and client peace of mind. Skellig is seeking a Senior MES Engineer with PAS-X and cGMP experience to support our clients across North America. To be considered for this role you must have PAS-X experience and experience working in biotech/pharma. Responsibilities
Lead small to large teams (depending on experience) to complete automation projects to fulfill client needs. Design, configure, implement, and test changes for new and existing Recipes, eLogs, Workflows, Work Instructions, Integrations, and system integration solutions on the client’s PAS-X system. Author, develop and execute validation test plans. Create basic project schedules that communicate progress and milestones. Support general project activities, including participating in client meetings, escalating issues, coordinating with the client’s vendors, and engaging with client support teams. Adhere to client procedures and maintain professional, respectful, and organized communication. Qualifications
Minimum of 2 years MES experience, preferably with PAS-X. Prior pharmaceutical industry experience. Experience working in biotech/pharma and with PAS-X is required. Project & Onsite Details
Projects are located at client facilities, typically large biotech manufacturing facilities with a dedicated PAS-X system. Engineers are required to be onsite at least 2–3 days a week, depending on client requirements. Benefits
Vacation / Personal Paid Time Off Sick Paid Time Off Paid Public Holidays Parental Leave Sabbatical Full health, dental, and vision PPO insurance for you and dependents (premiums fully covered) Life Insurance and Accidental Death and Dismemberment 401(k) Education Reimbursement Relocation package Company Culture
From its inception, Skellig has strived to be ‘more human.’ We foster a culture that promotes innovation, diversity, and great work, rewarding problem solving, teamwork, and service excellence. Our culture emphasizes honesty, transparency, and kindness—people-focused and compassionate. Application
Interested in building your career at Skellig? Apply through the form below to get future opportunities sent to your email. Apply for this job * indicates a required field First Name * Last Name * Email * Phone Country * Phone * Resume/CV * Enter manually Accepted file types: pdf, doc, docx, txt, rtf Education Degree LinkedIn Profile Website Voluntary Self-Identification
For government reporting purposes, we ask candidates to respond to the below self-identification survey. Completion of the form is voluntary and will not affect hiring decisions. Any information provided will be kept confidential. As part of Skellig’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected status under applicable law. This section describes categories of protected veterans and disability status to support our compliance with VEVRAA and OFCCP. Voluntary Self-Identification of Disability Form CC-305 OMB Control Number 1250-0005 (Expires 04/30/2026) Why are you being asked to complete this form? We are a federal contractor or subcontractor and must measure our progress toward a goal of having workers with disabilities. Completion is voluntary and confidential. For more information, visit the OFCCP website.
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