Automation Packaging Engineering Specialist
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| Job Type | Contractor |
| Area | Dublin, Ireland |
| Sector | Engineering |
| Start Date | |
| Advertiser | David Connolly |
| Job Ref | 1003132 |
| Job Views | 433 |
- Description
- 3132 - Automation Packaging Engineering Specialist
Team Horizon is seeking an Automation Packaging Engineering Specialist for a leading pharmaceutical company based in Dublin
Why you should apply:
Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
You enjoy working on exciting projects and want to work with a global manufacturing site in Dublin.
What you will be doing:
Work as part of a team to develop, implement and maintain packaging automation systems in the Manufacturing Facility.
Develop, review and approve new and updated software standards.
Provide automation expertise to the engineering and operations department on design and sustaining decisions.
Liaise closely with internal stakeholders to successfully support packaging operations.
Develop and implement standard operating procedures to ensure the future compliance of all automation systems.
Ensure all new software is delivered and maintained in a compliant and qualified state
Provide support for validation activities.
Participate in cross-functional teams to drive optimization of processes and equipment.
Assist in training personnel on specific automation aspects of equipment.
Design and implement solutions across automation platforms in line with the site change control procedures.
All other duties as requested or assigned.
What you need to apply:
5 years or more within the automation industry supporting GMP environments and applications.
3 years or more experience supporting a biopharma process.
Direct experience and in depth knowledge of packaging automation and vision systems platforms is required (preferably Seavision).
Direct experience in supporting a manufacturing facility.
Comprehensive understanding of cGMP requirements for clinical and commercial biopharmaceutical manufacturing and the ability to implement best practices (GAMP) to ensure site automation systems are cGMP compliant.
Full understanding of automation system implementation and validation life cycle along with an understanding of the product quality impact of changes.
Good interpersonal skills are required, as is the ability to communicate well, both verbally and written documents.
Knowledge of Automation systems design and experience of developing system architectures.
Direct experience in managing and working alongside system integrators.
Experience with, SQL Server and virtualization platforms is a plus, as is IT experience.
Experience with vendors Seavision, Marchesini.
Experience with China Serialisation (China ecoding)
