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. Its a goal that is grounded in efficiency transparency and our clients 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.
REQUIREMENTS:
- A minimum of 7 years Automation Experience Preferably with Syncade.
Prior Pharmaceutical industry experience
BENEFITS:
Heres whats waiting for you as one of our Senior MES Engineers
Vacation / Personal Paid Time Off
Sick Paid Time Off
Paid Public Holidays
Parental Leave
Sabbatical
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 clients facilities. Generally at a large biotech manufacturing facility with a dedicated Syncade otherwise noted in the job posting engineers are required to be onsite at least 2-3 days a week sometimes more depending on the clients requirements.
Your job will be to follow all client procedures to independently:
- 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 clients Syncade system.
- Author develop and execute validation test plans.
- Create basic project schedules that can be used to communicate progress and expected milestones.
- 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 clients vendors attending all required client training and engaging with the clients supporting teams.
Its important to be respectful compassionate a good communicator and well organized.
As with all our team members youll be extremely well looked after. Well make sure you receive all the back-up and support you need.
From its inception Skellig has strived to be more human. Wework hard to foster a culture that promotes innovation diversityand 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.
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. Its a goal that is grounded in efficiency transparency and our clients total peace of mind this is the vision be...
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. Its a goal that is grounded in efficiency transparency and our clients 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.
REQUIREMENTS:
- A minimum of 7 years Automation Experience Preferably with Syncade.
Prior Pharmaceutical industry experience
BENEFITS:
Heres whats waiting for you as one of our Senior MES Engineers
Vacation / Personal Paid Time Off
Sick Paid Time Off
Paid Public Holidays
Parental Leave
Sabbatical
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 clients facilities. Generally at a large biotech manufacturing facility with a dedicated Syncade otherwise noted in the job posting engineers are required to be onsite at least 2-3 days a week sometimes more depending on the clients requirements.
Your job will be to follow all client procedures to independently:
- 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 clients Syncade system.
- Author develop and execute validation test plans.
- Create basic project schedules that can be used to communicate progress and expected milestones.
- 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 clients vendors attending all required client training and engaging with the clients supporting teams.
Its important to be respectful compassionate a good communicator and well organized.
As with all our team members youll be extremely well looked after. Well make sure you receive all the back-up and support you need.
From its inception Skellig has strived to be more human. Wework hard to foster a culture that promotes innovation diversityand 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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