PharmEng Technology is a cGMP compliant leader with international operations in Canada, Spain, France, Germany, Austria, Switzerland, Italy, Belgium, Singapore, Malaysia, Indonesia, Taiwan, Ireland, Denmark, Brazil and USA and maintains strategic partnerships for extended capabilities internationally.
We are seeking a highly skilled MES Developer to work at our client site in LA.
This is a hybrid role.
As an MES Developer, you will play a crucial role in architecting, implementing, and integrating solutions that enhance manufacturing processes in a regulated environment.
Your technical expertise, attention to detail, and communication skills will be essential in leading cross-functional teams and delivering high-quality MES solutions.
Essential Duties and Responsibilities:
Architecting, implementing, and integrating solutions focused on tracking, analyzing, and improving manufacturing processes in a regulated environment.
Designing data management strategies for integrating MES solutions with JDE and plant automation equipment (DeltaV).
Conceptualizing solutions during the design phase of project life cycles.
Configuring, programming, debugging, and testing manufacturing execution systems (MES).
Creating documentation, including project design traceability documentation, test cases, and more.
Leading and guiding cross-functional teams from concept to deployment in MES projects of any size.
Engaging in customer-facing interactions and demonstrating technical communication skills.
Mentoring colleagues on MES expertise and knowledge base.
Technology Requirements:
ERP Platform: JDE
MES Platform: Siemens Opcenter Execution Process (formerly known as SIMATIC IT Unified Architecture for Process Industries)
Distributed Control System (DCS): DeltaV
Database Platforms: Microsoft SQL, Oracle, etc.
Project Documentation: Microsoft Office
Education and Skills Requirements:
Experience in MES Implementation, preferably Siemens Opcenter.
Minimum 5 years of working experience with JDE, Siemens Opcenter, DeltaV, and database platforms.
Minimum 5 years of working experience in the pharmaceutical/biotech industries.
Familiarity with FDA regulations and CFR 21 Part 11, cGMP.
Technical attitude with the ability to learn new systems quickly.
Demonstrated in-depth technical capabilities in system-supported manufacturing in a regulated environment.
Meticulous, conscientious, analytical, focused, and self-starter individual.
Excellent communication skills – both verbal and written.
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