Description:
\t\t\t\t\tSupport projects to establish manufacturing and improve existing production processes for a range of technically complex products (both medical device and non-medical device)Focus on project management, client and internal stakeholder communicationOwn product drawings, process flow charts, risk assessments, part critically lists, BOM management, supplier establishment and qualification, technical specifications, test fixture assembly, and test tool assessments
\t\t\t\t\tSkills:
\t\t\t\t\tMedical device, Manufacturing engineering, IQ OQ PQ, QMS, new product introduction, process improvement, CAPA, iso 9001, change management
\t\t\t\t\tTop Skills Details:
\t\t\t\t\tMedical device,Manufacturing engineering,IQ OQ PQ,QMS,new product introduction
\t\t\t\t\tAdditional Skills & Qualifications:
\t\t\t\t\tBachelor's degree in engineering or related area of study 3+ years of previous experienceDemonstrated experience in new product developmentExperience in change management and process improvement
\t\t\t\t\tExperience Level:
\t\t\t\t\tIntermediate Level
About ActalentActalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our peopleThe company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
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