Student Veterans of America Jobs

Welcome to SVA’s jobs portal, your one-stop shop for finding the most up to date source of employment opportunities. We have partnered with the National Labor Exchange to provide you this information. You may be looking for part-time employment to supplement your income while you are in school. You might be looking for an internship to add experience to your resume. And you may be completing your training ready to start a new career. This site has all of those types of jobs.

Here are a few things you should know:
  • This site is mobile friendly. You do not need a log-in or password to access information.
  • Jobs on this site are original and unduplicated and come from three sources: the Federal government, state workforce agency job banks, and corporate career websites. All jobs are vetted to ensure there are no scams, training schemes, or phishing.
  • The site is refreshed daily to remove out-of-date content.
  • The newest jobs are listed first, so use the search features to match your interests. You can look for jobs in a specific geographical location, by title or keyword, or you can use the military crosswalk. You may want to do something different from your military career, but you undoubtedly have skills from that occupation that match to a civilian job.
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Terumo BCT Global Quality Manager in Lakewood, Colorado

Global Quality ManagerDate: Nov 5, 2019Location:Lakewood, CO, US Company: Terumo BCT, Inc.Requisition ID: 23554JOB SUMMARYLeads specified Quality Management Systems team supervising detailed work on aspecific portion of a broader task assigned to experienced qualityspecialists. The Quality Manager will play an integral role in interpretingregulations and standards into Terumo BCT policies and procedures, andowning the ongoing maintenance, execution, and improvement of their QMSarea(s) of responsibility. Support and improve various Quality Systemprocesses to maintain regulatory compliance.ESSENTIAL DUTIESQMS areas of ownership, management, and responsibility may include (asassigned): CAPA, Audit (internal, external, supplier), PostMarket Surveillance (recalls / field actions, product risk review,post-market data review), Quality System Training, Document Control,ManagementServes as expert and main point of contact for regulatory / complianceissues within area of responsibility.Acts as the policy / procedure owner for area(s) of responsibility,ensuring they are compliant and effective.Executes their QMS area(s) in accordance with governing internal policies/ procedures and external standards and regulations. This likelyincludes: generation and approval of annual schedules, execution toschedule, approval of plans or reports, follow up on action items,facilitation of discussions with participants and stakeholders to ensuresuccess and compliance.Monitors the health of the QMS areas(s) within their area ofresponsibility, and provides metrics to management as required, includingany governing oversight boards.Identifies and implements continuous improvement opportunities within theirarea(s) of responsibility.Serves as Subject Matter Expert and Process Owner for their QMS area(s) ofresponsibility during audits and inspections.Influences the organization in quality objectives, prioritization andresourcing decisions as necessary.Manages team of direct reports in support of the above (as applicable).Manages and provides operational leadership for the functional group'sdevelopment, direction, and effectiveness, adhering to organizationalpolicies and processes and supporting overall business and corporateobjectivesActs as an internal champion for quality initiatives aimed at improvingbusiness systems and compliance; may be the primary representative ofQuality group on projects.During audits and inspections, interfaces with global regulatoryauthority, notified body auditors and provides general support for theQuality group.Interfaces with QMS area owners and project teams from other Terumo BCTlocations, regions, and corporate.MINIMUM QUALIFICATION REQUIREMENTSEducationBachelor's degree or, equivalent of education and experience sufficient tosuccessfully perform the essential functions of the job may be considered.ExperienceMinimum 5 years experience.Candidate must have experience in the post market process. Specifically,candidate must be experienced and knowledgeable in the Field Action process,including execution and advising the organization globally on suchrequirementsPreferred minimum 7 years experience in Quality Assurance and or RegulatoryAffairs, involving US FDA Class II or Class III medical devices includingknowledge .and. experience of applying global device laws .and. regulations foradverse event reporting and product recalls.Minimum 2 years supervisory experience.Preferred training in FDA Quality System Regulation and ISO 13485.SkillsKnowledge of U.S. and international medical device regulations and standards(CFR 820, MDD and ISO 13485).Post Market Surveillance process, and knowledge of EU MDR requirements inthis regard would be a plus.Strong interactive skills in cross functional participation and influence,mentoring and acceptance of guidance, technical leadership, projectmanagement, coordination with cross functional team member, teambehavior, and support for subordinates, quality speciali