Job Description:Strong written and verbal communication skills.Possess strong analytical and problem-solving skills.Familiarity with one of SAS, JMP, or Minitab is strongly desired.Working knowledge of MS Office, including Office Project software.Six Sigma Process Improvement Experience/Certification desirable.Regulated industry experience preferred.Familiarity with cGMP practices desired.Outstanding team player who seeks and values diverse input to hone ideas, but who has the experience to develop strong starting proposals.Highly motivated, self-starter.Responsibilities:Lead, plan, manage and implement supplier capital qualifications from kick-off to implementation into production. CollaborationGenerate or review supplier validation/qualification protocols and coordinate their execution and final reporting.Lead with teamwork and drive for results; able to work in a borderless organization and across multiple functions including, programs, engineering, purchasing and suppliers.Lead teams responsible for the procurement and installation of manufacturing equipment at global suppliers.All other duties as assigned.Requirements:3 years of relevant experience.BS Engineering Degree (Plastics, Mechanical, Manufacturing/Industrial) or related field.Ability to manage Supply Chain projects concept to production, including the authoring and oversight of IQ/OQ/PQ protocols for component manufacturing processes and secondary.Experience within an FDA regulated industry.Minitab is strongly desired or JMP.
