Manufacturing Engineering Support

*Please strictly adhere to the following resume naming convention:
ALL CAPS NO SPACES B/T UNDERSCORES
PTNUSGBAMSREQIDCANDIDATEBEELINEID
i.e. PTNUS9999999SKIPJOHNSON0413

Bill Rate $ 42/hr

MSP Owner: Felix Avalos
Location: Warsaw IN
Duration: 6 months
GBaMS ReqID:





Role Descriptions:
Essential Skills: TechnicalFunctional Skills Experience supporting medical device manufacturingProcess ValidationsSpecific experience with process characterization equipment IQOQ process OQ and PQSpecific experience with Test method Validation and Gage RRExperience with root cause analysis and problem-solving for both technical and process issuesWorking knowledge of design control and cGMP requirements for medical device manufacturing per FDA QSR and ISO13485-2003Ability to lead and prioritize multiple medium-complexity project assignments and complete work in a timely mannerGood problem-solving skills using quality and statistical toolsBOM Router creation and updateAbility to read and understand engineering drawingsKnowledge of basic quality tools risk analysis (PFMEA) statistics (SPC) Critical-to Quality (CTQ) AnalysisKnowledge of Quality System requirements ISO and FDA requirementsAbility to effectively work within a cross-functional team to complete critical project tasksDemonstrates good written and verbal communication skillsExperienced with control procedures such as the Change Management System Nonconformance Reports Engineering Specifications Corrective and Preventive Action (CAPA) and Work Instructions Proficient with Statistical Process Control conceptsMicrosoft Office Suite and ProjectExperience Required4 - 6 yearsRoles ResponsibilitiesDevelops and Executes Process Validation Strategies Creates plans protocols (IQ OQ PQ) and risk assessments to ensure effective processes for medical devices and Regulatory Compliance Adheres to FDA (21 CFR 820) ISO 13485 and other relevant regulations participating in audits and maintaining up-to-date Data and Reports Findings Compiles and analyzes validation data writes comprehensive reports and identifies trends for process Cross-Functionally Works with Manufacturing Quality Assurance Engineering and other teams to implement cleaning strategies resolve issues and provide technical continuous improvement initiatives manages change controls troubleshoots cleaning problems and ensures proper documentation and training. Creating maintaining and improving controlled technical documents such as prints procedures bills of materials and a wide variety of processing applications such as machining finishing forging casting cleaning heat treating bonding molding feasibility study to estimate a product cost and analyze capital equipment capacity and capability requirementsEstablishing and improving process methods that meet performance and quality requirementsDeveloping and executing project plans and schedules for work activitiesCommunicate (written and verbal) direction and project plans with appropriate personnel from other multiple options to select the most appropriate processes and machining me
Desirable Skills:
Keyword:
Skills: EIS : Manufacturing Engineering Support
Experience Required: 4-6