Minimum experience of 4 years in Medical devices - Manufacturing Engineering.
Good Experience working on Process Validations (IQ, OQ, PQ)
Experience developing manufacturing processes and technologies, which includes process characterization
Experience working on PFMEAs
Experience performing Data analysis (Minitab)
Evaluate process and design alternatives based on Design for Manufacturability principles.
Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
Multitasks, prioritizes and meets deadlines in timely manner.
Strong organizational and follow-up skills, as well as attention to detail.
Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
Numbers & Facts
Location
Plano, TX
Industry
Other/Not Classified
Company Size
100 to 499 employees
Skills
Communication Skillsunmatched
Corporate Policiesunmatched
Data Analysisunmatched
Detail Orientedunmatched
Establish Prioritiesunmatched
FDA (Food and Drug Administration)unmatched
FDA Requirementsunmatched
Follow Throughunmatched
Manufacturing Designunmatched
Manufacturing Engineeringunmatched
Manufacturing/Industrial Processesunmatched
Medical Equipmentunmatched
Minitabunmatched
Multitaskingunmatched
Operations Processesunmatched
Organizational Skillsunmatched
Presentation/Verbal Skillsunmatched
Process Developmentunmatched
Process Validationunmatched
Regulatory Requirementsunmatched
Time Managementunmatched
Writing Skillsunmatched
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