MES Lead Engineer

whatchado GmbH; Langenfeld (Rheinland); Vor Ort; EUR 60.000 - 100.000; Vollzeit

Zusammenfassung

Ein etabliertes Unternehmen sucht einen MES Lead Engineer, der für die Gestaltung und Implementierung von Manufacturing Execution Systems verantwortlich ist. In dieser Rolle arbeiten Sie eng mit Kunden in der pharmazeutischen und biotechnologischen Industrie zusammen, um maßgeschneiderte Lösungen zu entwickeln, die den höchsten Standards entsprechen. Sie werden die Möglichkeit haben, Ihre technischen Fähigkeiten in einem dynamischen Umfeld einzusetzen, während Sie gleichzeitig die Verantwortung für die Projektleitung und die Schulung von Teams übernehmen. Wenn Sie eine Leidenschaft für innovative Technologien haben und gerne in einem kollaborativen Team arbeiten, ist dies die perfekte Gelegenheit für Sie.

Leistungen

Flexible Home-Office-Regelung

Umfassende medizinische Versorgung

Wettbewerbsfähige Sozialleistungen

Möglichkeiten zur beruflichen Weiterentwicklung

Globale Freiwilligengruppen

Qualifikationen

• Erfahrung in der Softwareentwicklung mit C#, C++ oder VB.Net erforderlich.
• Kenntnisse in der FDA-regulierten Industrie und cGMP sind von Vorteil.

Aufgaben

• Leitung der Implementierung von MES-Projekten in der pharmazeutischen Industrie.
• Entwicklung von Designs, die den Kundenanforderungen entsprechen.

Kenntnisse

C#

C++

VB.Net

Web Services

ASP.Net

XML

Requirements Analysis

System Integration

Project Leadership

English (written and spoken)

German (fluent)

Ausbildung

Technical University Degree in Computer Science

Chemical Engineering

Control System Engineering

Tools

Syncade

Rockwell ProPack Data

Werum PAS-X

SAP

DeltaV Control System

Jobbeschreibung

MES Lead Engineer

We are looking for a Manufacturing Execution System Lead Engineer to join our team in Langenfeld, Germany!

In this role you will be responsible for overall design and engineering of project specific Manufacturing Execution Systems (MES), primarily in the pharmaceutical and biotech industry, to meet the requirements of both the end-users and Emerson Process Management business.

If this sounds like an interesting job for you, then join our team at Emerson!

In This Role, Your Responsibilities Will Be:

• Architect and lead the implementation of MES and system integration solutions projects following Emerson Project Management Office and Quality Control Processes to clients primarily in the biotech and pharmaceutical industry.
• Guide customers in defining optimal ERP/ LIMS/ etc. interfaces and ensure their detailed design and efficient deployment.
• Develop designs that meet client requirements and documentation required for validated facilities.
• Be responsible for the overall solution, to define scope, sizing, system / operational requirements/integration/functional requirements, support project estimations and ensure execution methodology.
• Provide project execution leadership and mentorship at different levels within project teams, client organizations and sales, as well as with an experienced team of sales engineers, consultants and software developers.
• Install and commission MES software applications including commercial products and internally developed applications, in-house and at customer site.
• Visit client sites and perform design studies, acceptance tests, commissioning and training.
• Quickly learn new skills and technologies.
• Assist the sales organization in demonstrations, presentations and engineering estimates.

Who You Are:

You model high standards of honesty and integrity. You pursue everything with energy, drive, and the need to finish. You observe situational and group dynamics and select best-fit approaches.

For this Role, You Will Need:

• Technical University Degree or equivalent experience in Computer Science, Chemical Engineering or Control System Engineering and experience with requirements analysis, design definition and implementation of software solutions above the manufacturing floor.
• Experience with software development using C#, C++ or VB.Net and Web Services, ASP.Net and XML.
• Experience in FDA regulated industry- knowledge of cGMP, 21 CFR part11 and validation.
• Experience with Manufacturing Execution System packages like Syncade, Rockwell ProPack Data, Werum PAS-X and proven experience in a MES project leadership role.
• Experience with integrating different plant floor / MES / ERP systems (SAP preferred).
• Knowledge of some, preferably all, of the following DeltaV Control system elements: Software system design, System software engineering with Batch and Recipe applications, Software implementation and software testing.
• Proficiency in English - written and spoken and fluent German.
• Availability to travel within Germany, Austria and Switzerland (valid car driving license) up to 20% of the time.

Preferred Qualifications that Set You Apart:

• Proven MES product knowledge or software development experience preferred.
• Experience biotech/pharmaceutical sites preferred.
• Batch plant operation experience preferred.

Our Offer to You:

We understand the importance of work-life balance and are dedicated to supporting our employees' personal and professional needs. From competitive benefits plans and comprehensive medical care to equitable opportunities for growth and development we strive to create a workplace that is supportive and rewarding.

Depending on location, our flexible work from home policy allows you to make the best of your time, by combining quiet home office days with collaborative experiences in the office so that you can personalize your work-life mix.

Moreover, our global volunteer employee resource groups will empower you to connect with peers that share the same interest, promote diversity and inclusion and positively contribute to communities around us.