10 years of MES experience in Manufacturing and Medical Device Domain (MDD).
5 years of working experience in managing Critical Manufacturing MES implementations and Rollouts master data modelling and enrichment.
Certified Critical Manufacturing Professional Associate.
Must have basic knowledge or understanding of Pharmaceutical Medical Device compliances like 21 CFR Part 11 Compliance GAMP GDP etc.
Previous work experience in MES implementation using any platform.
Must have hands-on experience on testing tools like HP ALM Polarion etc.
Excellent English skills both spoken and written.
Collaborate as a project team member and directly with customers on requirement gathering master data modelling and enrichment giving Demos on core and new concepts to SMEs and End users.
Working collaboratively and helping cross-cultural and cross-regional team members both internal and on the customer side.
Develop and produce technical reports process flow diagrams and documentation in support of design and developments.
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.