MES Engineer
- United States
- Contract
- CAPEX Projects
This vacancy has now expired
Our client, a global Pharmaceutical manufacturing organization are looking for a talented MES Engineer to join their expanding team. With continued organizational growth and considerable investment across their portfolio and capital programs this is an extremely exciting opportunity to contribute towards their brand-new manufacturing facility on the East Coast of the United States.
Responsibilities:
- Support the design and implementation of an MES system for the Drug Product and Finished Goods facility
- Leverage PAS-X design and code prepared from similar project in the EU
- Interface with the IT/OT and I&C teams for coordination and integration of the MES to systems such as SAP and PI
- Collaborate with process engineers, product engineers, quality, and production managers to optimize production processes
- Leverage Master Batch Records, MES documents, and SOPs from the EU and adapt them to support the client
- Utilize the existing Master Batch Record templates to create new records when applicable
- Test MES interfaces to IT systems and equipment, Equipment Statuses, Master Batch Records, and Approval Workflows before going live in the Production environment
- Periodic International and Domestic travel may be required
- You should expect the role and responsibilities to expand into equipment support as the project enters startup and qualification activities
Knowledge and Skill; We are looking for a candidate with the following background and skill sets:
- Bachelor’s degree in Chemical, Electrical, Computer Science, Biological Science or equivalent
- Collaborative attitude with the willingness to work with global peers and cross-functional teams toward company and department goals
- 5+ years’ experience designing, configuring, and implementing Automation control systems
- 2+ years’ of direct experience with MES application development and deployment preferred
- Preference of having experience with Körber’s PAS-X MES software
- Experience with working with OEMs to develop integration strategies into ERP and SCADA systems preferred
- Excellent oral and written communications skills and fluency in English
- Experience in a cGMP facility or working with FDA regulations, or similar regulated industries
- Knowledge with Drug Product (DP), and/or Finished Goods Manufacturing (FGM) would be beneficial
- Knowledge with Körber PAS-X, SAP (interfaces), OSIsoft PI, and Siemens PLCs is a plus
If this role is of interest to you, please apply now!
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
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