This client is seeking a Senior MES Engineer with Syncade and cGMP experience to support their 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:
Here's what's waiting for you as one of their 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:
Their projects are based at their client's facilities. This role would be fully remote, but generally, at a large biotech manufacturing facility with a dedicated Syncade system.
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 client's 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 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.
