SL Controls provides Equipment System Integration solutions to manufacturers, particularly those in the life sciences and technology sectors. Due to the ongoing growth and expansion of our business, we have a number of exciting engineering career opportunities available.
The roles are based in various locations across Ireland as well as in our office in the USA. Our engineers deliver cutting-edge Smart Factory and Industry 4.0 solutions, so the work is rewarding and challenging. We also offer excellent opportunities for career progression.
The Role:
* MES Integration Engineer
* Dublin
* Hybrid role - you will be expected to be onsite in South Dublin typically 3 or 4 days per week so you must be able to commute to site as required
* Permanent or Contractor opportunity
Role Brief:
This role will be responsible for the delivery of new and updated integration functionalities for Manufacturing Information Systems for use in production.
Core Responsibilities:
* Development, configuration and testing for integration components of Master Batch Records (MBRs) from initial to final design
* Leading integration development design reviews including liaising with Automation, Operations, Process Development, Validation and Quality functions
* Equipment integration design, configuration and testing to allow MBR interaction with shop floor equipment and lab equipment for in-process testing
* Liaising with Plant Support, System Owner and Operations teams regarding documentation changes in an effective and timely manner
* Responsible for the MBR design oversight, support and ongoing development of the client site MES system
* Training of Electronic Batch Record (EBR) designers and end-users on MES integration activities and development of job aids
* Support and assist in fast Manufacturing Execution System (MES) issue resolution where required and as directed by Operations leadership
* Development, review and update MES Standard Operating Procedures and Design Specifications
* Contribute to extending our MES solution and developing project & technical skillset in collaboration with our team and Vendor consultants.
Skills Brief:
* Experience in an IT/Software focused role in a GMP (Pharma, Life Sciences, Medical Devices, Biotech) manufacturing environment is essential and only candidates with some experience in this area will be considered.
* Working knowledge of drug product manufacturing and packaging in pharmaceutical/biotech industries or aseptic processing.
* MES experience (Preferably Werum PAS|X) with focus on workflow, S95 & S88 standards and integration from the control layer to MES in pharma & bio-pharma industries
* Knowledge of regulation requirements (including cGMP, 21CFR Part11)
* Knowledge of Quality Systems (e.g. Veeva Vault, NC/CAPA)
* Knowledge of validation processes and understanding of validation protocol generation requirements
* Knowledge of computer systems applicable to responsibilities (e.g. MES, ERP, SCADA, PLC, Historian)
* Strong capabilities in S95 level 2 and level 3 systems and their integration
Person Brief:
* A Bachelor's degree in computer science or an IT related discipline is preferred or a highly related qualification in mechatronics or manufacturing engineering will also be considered.
* 4 years plus experience working in an MES Software environment with direct manufacturing industry exposure is essential.
* Strong analytical, troubleshooting, written & verbal communication skills are essential.
* The role is based onsite in Dublin so you must be living in the area or able to relocate in a short time frame and be able to be onsite daily.
Opportunity Brief:
This is an excellent opportunity to work with clients who are global leaders in their field, helping to develop and improve upon industry leading technology solutions. NNIT Ireland offers a supportive environment committed to employee development and wellness, along with a competitive and rounded compensation package, which rewards high performers.
Company Brief:
NNIT Ireland are experts in the area of Equipment System Integration and System Support. We specialise in assisting our customers, including many of the world's top multinational companies in the medical device and pharmaceutical sectors, achieve their Six Sigma and OEE targets.
For over 20 years we have grown our business from a Sligo based enterprise into an international business with additional offices in Galway, Limerick, Leinster and Florida USA.
We pride ourselves on our expertise in industrial IT integration and regulatory compliance in support of global end users, OEM's and Technology providers.