19 Apr
Manufacturing Engineer
Indiana, Warsaw 00000 Warsaw USA

Vacancy expired!

Job Description

Job Description : Experience in virtual team management and onsite / offshore coordination

The Candidates should have experience in Manufacturing Engineering

Site specific data collection across all relevant sites (Extract data from ERP systems like SAP, MES-CAMSTAR and JD Edwards)

Experience in data mining, analysis and formulation

Experience in medical device manufacturing process, process flow and process mapping, quality system, validation and risk assessment

Experience in technical documentation / business case / change order - writing, reviewing and routing documentation

Experience in packaging processes and value chain analysis

Knowledge in sterility assurance / microbiology, cleaning validation, verification / validation, assessment of risk and mitigation plans

Knowledge in product life cycle management, NPI / NPD, and cGxP

Knowledge in EU-MDR, FDA CFR Title 21, ISO 13485:2016 and understanding of regulatory requirements

Experience in formulating WBS, creation of work packets and structuring the scope at project level

Excellent communication and stakeholder management

Excellent team player with leadership skills

Experience in Microsoft Excel, PowerPoint and Project

Knowledge of Project Management is value addition to project

Site specific data collection across all relevant sites (Extract data from ERP systems like SAP, MES-CAMSTAR and JD Edwards)

Experience in data mining, analysis and formulation

Experience in medical device manufacturing process, process flow and process mapping, quality system, validation and risk assessment

Experience in technical documentation / business case / change order - writing, reviewing and routing documentation

Experience in packaging processes and value chain analysis

Knowledge in sterility assurance / microbiology, cleaning validation, verification / validation, assessment of risk and mitigation plans

Knowledge in product life cycle management, NPI / NPD, and cGxP

Knowledge in EU-MDR, FDA CFR Title 21, ISO 13485:2016 and understanding of regulatory requirements

Experience in formulating WBS, creation of work packets and structuring the scope at project level

Excellent communication and stakeholder management

Excellent team player with leadership skills

Experience in Microsoft Excel, PowerPoint and Project

Knowledge of Project Management is value addition to project

Education :Bachelor’s degree in Engineer, Science or Equivalent

Additional Information

All your information will be kept confidential according to EEO guidelines.

Vacancy expired!


Related jobs

Report job