Skills
- Hands-on experience with Manufacturing Execution Systems (MES) preferably with Critical Manufacturing platform.
- Strong understanding of manufacturing operations production processes and shop floor workflows in regulated industries
- Medical device pharmaceutical preferred
- Experience with MES configuration customization and integration with enterprise systems (ERP QMS PLM).
- Experience with software testing QA validation and requirements documentation.
- Technical proficiency in system integration approaches including APIs web services and middleware platforms.
- Experience with FDA 21 CFR Part 11 and other regulatory requirements for electronic manufacturing records.
PREFERRED QUALIFICATIONS
If this person implemented Critical Manufacturing MES platform.Familiarity with data analytics and reporting tools for manufacturing intelligence.Experience with serialization track and trace and genealogy requirements.Job Title
MES Technical Manager (Supply Chain Operations)
Start date & Location
Onsite 5 days Andover MA
Position Notes
Job Description : POSITION SUMMARY
TransMedics is launching a major initiative to transform its Manufacturing Execution System (MES) operations and we are seeking a hands-on Technical Lead to perform the technical and operational aspects of this effort. This is an individual contributor role with a strong focus on manufacturing operations technology shop floor systems and end-to-end production process orchestration. This role requires deep Critical Manufacturing MES platform expertise strong technical integration skills and a proactive approach to problem-solving. The ideal candidate will bring a strong manufacturing and production background understanding of shop floor operations and equipment integration deep knowledge of industrial IoT and regulatory compliance requirements and the ability to bridge IT and manufacturing operations. This role will be instrumental in configuring and optimizing the MES platform supporting integrations and driving system testing and validation.
RESPONSIBILITIES
Lead the technical execution of the MES transformation project ensuring it is configured correctly and meets production operational requirements.Define and document technical configurations and integration requirements in collaboration with Manufacturing Operations Production and Supply Chain teams.Perform software configuration and system integration testing to ensure MES functionality and alignment with manufacturing workflows and business needs.Act as a technical MES expert supporting platform configuration customization testing and implementation.Collaborate with Manufacturing Operations to ensure MES capabilities meet shop floor requirements and production tracking needs.Support production engineering and quality teams in transitioning to the new digital manufacturing workflows and real-time data capture processes.Drive hands-on execution of system configuration integration testing validation and production workflow mapping activities.Design and implement integrations between Critical Manufacturing MES and enterprise systems (ERP QMS PLM etc).Configure shop floor data collection equipment interfaces and manufacturing process definitions within the Critical Manufacturing platform.Provide input into future MES governance structure and technical roadmap as the manufacturing technology function matures.MANAGEMENT RESPONSIBILITIES
No direct reports (This position will not have management responsibilities).PHYSICAL ATTRIBUTES
None (Standard office environment).MINIMUM QUALIFICATIONS
Bachelors degree in Information Systems or related field.Years of hands-on experience with Manufacturing Execution Systems preferably with Critical Manufacturing platform.
Strong understanding of manufacturing operations production processes and shop floor workflows in regulated industries (medical device pharmaceutical preferred).Demonstrated experience with MES configuration customization and integration with enterprise systems (ERP QMS PLM).Experience with software testing QA validation and requirements documentation.Technical proficiency in system integration approaches including APIs web services and middleware platforms.Knowledge of FDA 21 CFR Part 11 and other regulatory requirements for electronic manufacturing records.Strong analytical and problem-solving skills with ability to translate manufacturing requirements into technical solutions.Excellent communication skills with ability to work effectively with both technical and operational stakeholders.Self-motivated with ability to work independently and manage multiple priorities in a fast-paced environment.PREFERRED QUALIFICATIONS
Direct experience implementing or supporting Critical Manufacturing MES platform.Experience in medical device or other highly regulated manufacturing environments.Knowledge of Industry 4.0 concepts Industrial IoT and smart manufacturing initiatives.Familiarity with data analytics and reporting tools for manufacturing intelligence.Experience with serialization track and trace and genealogy requirements.Key Skills
Inventory Control,Procurement,SAP,Supply Chain Experience,SAP Supply Chain Management,Production Planning,Supplier Management,ERP Systems,Materials Management,Logistics,Manufacturing,MRP
Employment Type : Full Time
Experience : years
Vacancy : 1