Ihre Vision ist ehrgeizig. Genau wie bei uns.
Unsere Mitarbeiter sind unser Erfolg. Als einer von uns tragen Sie zur technischen Spitzenleistung für die High-Tech-Märkte der Zukunft bei, darunter Halbleiter, Batterien, Pharmazeutika, Biotechnologie und Rechenzentren. Bei Exyte werden Sie Teil einer globalen Gemeinschaft von Herausforderungssuchenden, die ehrgeizig und leidenschaftlich für Innovation sind. Gemeinsam werden wir auf der langen Geschichte unseres Unternehmens aufbauen und weiterhin den Weg in eine bessere Welt weisen.
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The Senior (Sr) Expert Quality Management will be responsible for ensuring that all subcontractor work on site complies with project design documents, industry standards, and local, state, and federal building codes. This position requires extensive knowledge of high-tech facility construction, particularly in semiconductor or biopharma environments, to ensure the highest quality and safety standards are maintained throughout the project lifecycle. In addition, this role requires to act as client interface and client appointed third party QAQC interface to ensure all project specific plan, specifications are followed and guide contractor QC and Exyte QC accordingly
Explore Your Tasks And Responsibilities•Leadership & Expertise: Provide overall leadership and guidance on all the Project QA/QC Team to ensure successful execution. Provide coaching and guidance to subcontractors and Exyte Team regarding best practices, industry standards, and specific project requirements.
•Code Compliance & Safety: Validate final installations do not violate code requirements, including equipment clearances, emergency egress paths, and other safety aspects. Enforce the Company Safety Policy on-site and pay due diligence to safety aspects at all times, ensuring compliance with site-specific safety protocols.
•Meetings & Collaboration: Attend kick-off and clarification meetings with subcontractors and suppliers to ensure alignment on project requirements and expectations. Attend and actively participate in Quality Meetings with the project Owner, subcontractors, and other stakeholders to discuss quality control issues and solutions.
•Documentation & Reporting: Maintain clear and concise documentation of inspections and audits. Ensure that all reports are completed and submitted on time. Identify and issue Non-Conformance Reports (NCRs) where work does not meet design or specification requirements. Follow up to ensure NCRs are addressed and closed out.
•Integrated Quality Assurance and Quality Control Planning: Develop, coordinate, and execute an Integrated Quality Plan, working closely with all the departments to align activities.
•Perform additional duties as assigned by management to ensure the successful completion of the project.
•Analyzes QA/QC elements and report to the Project Quality Manager
•Reviews in detail and approves of subcontractors and suppliers Quality Plans and issues report thereon.
•Reviews specifications to identify all testing and inspections required and consolidates into unified testing matrix. Also, he/she can propose additional test(s), which are not included in the testing matrix, if deemed necessary
•Ensures that all information required by the Project Quality Plan and specifications are submitted and complies with Owner requirements and specifications, and is continually reviewed through the project duration
•Identifies deviation and non-conformities and participates in the process of Non-Conformance Reports (NCR) and propose technical solutions.
Show Your Expertises
•Bachelor’s degree in engineering (the required education degree may be substituted by extensive professional experience involving similar work responsibilities and/or additional training certificates in relevant domains)
•12+ years of experience in high-tech facility construction, with a strong emphasis on quality assurance and control.
•Proficient in reading and interpreting design documents, building codes, and project specifications.
Preferred
•Experience in Semiconductor or Biopharma Life Sciences facility construction strongly preferred.
•Strong knowledge of semiconductor or biopharma facility construction methods and quality control standards.
•Experience with performing and documenting field inspections, ensuring all work meets quality and regulatory requirements.
•In-depth knowledge of relevant building codes, industry standards, and project specifications.
•Exceptional conflict resolution and communication skills, with the ability to work effectively with stakeholders at all levels.
•Proficiency with Microsoft Office Suite, BIM360, and other construction management software.
•Ability to work collaboratively with diverse teams, maintaining positive relationships with subcontractors, suppliers, and stakeholders.
•Strong leadership skills, with the ability to coach subcontractors on best practices and industry standards.
•Excellent verbal and written communication skills, with the ability to clearly convey technical information to non-technical stakeholders.
Kontakt
Clinton Crellin
Exyte ist ein Arbeitgeber, der sich für Chancengleichheit bei der Beschäftigung einsetzt und sich für Chancengleichheit und Gleichbehandlung einsetzt. Daher bietet die Exyte Group allen qualifizierten Bewerbern gleiche Beschäftigungsmöglichkeiten, unabhängig von Abstammung, Geschlecht, sexueller Orientierung, Geschlechtsidentität, Rasse, Hautfarbe, Religion, geschütztem Veteranen- oder Behindertenstatus oder genetischen Informationen.
Boise, ID
full_time
