IT System Lead - Production Systems (Manufacturing)
IT System Lead - Production Systems (Manufacturing)
Posted on :
21-05-2025
Employer Active
1 Vacancy
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Share
Send me jobs like this
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Job Description
Our client a global healthcare company is looking for a highly skilled IT System Lead to oversee production systems across our client s global manufacturing facilities. This role will act as the System Owner for critical production applications including MES (Manufacturing Execution Systems) serialization platforms Historian systems and SAP interfaces. The ideal candidate will possess deep technical and functional expertise in manufacturing processes within regulated environments.
This is a contractual position through the end of 2025. With the likelihood of an extension into 2026. Occasional travel will be required to the clients plant facilities located in St. Wendel Germany & LArbresle France.
Key Responsibilities
- Serve as the primary owner for production systems (MES serialization Historian SAP interfaces) ensuring reliability compliance and optimization.
- Lead troubleshooting upgrades and integration efforts to align with manufacturing and regulatory requirements.
- Provide technical guidance for discrete batch and manual production processes in regulated industries (e.g. pharmaceuticals medical devices).
- Ensure systems adhere to industry standards (e.g. GxP FDA EU regulations).
- Partner with crossfunctional teams (IT operations QA) to translate business needs into technical solutions.
- Train endusers and support teams on system functionalities and best practices.
- Maintain system validation audit trails and documentation to meet regulatory expectations.
- Implement risk mitigation strategies for systemrelated issues.
Requirements
- 5 years of handson experience with MES serialization systems (e.g. Track & Trace) Historian (e.g. OSIsoft PI) and SAP interfaces in manufacturing.
- Proficiency in production processes (discrete batch manual) within regulated environments.
- Familiarity with compliance frameworks (GxP FDA 21 CFR Part 11 EU Annex 11).
- English fluency (mandatory); German or French proficiency is a strong advantage.
- Bachelor s degree in Computer Science Engineering or related field. Relevant certifications (e.g. MES Professional SAP) are a plus.
- Willingness to travel occasionally to EU plant locations.
Preferred Qualifications
- Experience in pharmaceutical medical device or similarly regulated manufacturing sectors.
- Knowledge of IoT/Industry 4.0 technologies and digital transformation initiatives.
Employment Type
Full Time
Key Skills
Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.
