Adjunto Dirección Fiscal – Estrategia Tributaria Global

Grupo Térvalis; Valencia; Vor Ort; EUR 90.000 - 120.000; Vollzeit

Zusammenfassung

Celestica in Valencia, Spain is seeking a Senior Quality Manager focused on New Production Introduction (NPI) to lead the design and deployment of QMS processes across healthtech sites.

You will drive DFx reviews, validate IQ/OQ/PQ plans, manage launch readiness, and ensure ISO 13485 and related standards are met while monitoring performance through scorecards and audits. The role requires 15+ years in quality management and a proven ability to build capable cross-site teams.

Qualifikationen

• Bachelor's Degree or higher in Engineering or Quality Management with industry certifications preferred (ASQ, Six Sigma, ISO13485 Lead Auditor).
• Extensive experience implementing QMS for NPI and manufacturing scale-up across global sites.
• Strong analytical and problem-solving skills with data-driven decision making.

Aufgaben

• Lead the design and deployment of QMS processes to meet NPI objectives and customer requirements.
• Drive DFx reviews and oversight on validation strategies (IQ, OQ, PQ) for smooth design-to-mass production transitions.
• Manage launch readiness assessments, Monthly Operations Reviews, and customer satisfaction surveys.
• Ensure site-wide conformance to ISO 13485 and related regulations and certifications.
• Analyze quality data, communicate gaps, and define action plans with stakeholders.
• Develop and own global QMS processes to mitigate operational risks.
• Document and deploy global quality procedures across sites and train teams accordingly.

Kenntnisse

Quality Frameworks

NPI Quality Planning

Advanced Quality Tools

Validation & DFx

Performance Analytics

Ausbildung

Bachelor's Degree or higher in Engineering/Quality Management

Jobbeschreibung

Req ID:

Remote Position: No

Region: Europe

Country: Spain

State/Province: La Pobla De Vallbona

City: Valencia

Summary

Senior Quality Manager - New Production Introduction (NPI) Focus

Detailed Description

• Quality Planning & Strategy: Lead the design and deployment of Quality Management Systems (QMS) processes and tools to ensure NPI objectives and customer requirements are met.
• DFx & Technical Readiness: Drive Design for Excellence (DFx) reviews and oversight on validation strategies (IQ,OQ,PQ) to ensure seamless product transitions from design to mass production.
• Launch Readiness: Manage launch readiness assessments, Monthly Operations Reviews, and Customer Satisfaction Surveys to ensure operational excellence at the HealthTech sites.
• Regulatory Oversight: Ensure site-wide conformance to international regulations and customer certifications (e.g., ISO 13485, ANSI/ESD ).
• Performance Monitoring: Analyze data from customer scorecards, regulatory audits, and operational performance to identify gaps and communicate action plans to stakeholders.
• Global QMS process ownership: Develop and support key QMS processes to ensure regulatory compliance and mitigate operational risks.
• Process Deployment: Document and deploy global quality processes (Audit Compliance, Customer Feedback) in alignment with strategic corporate initiatives.
• Training & Capability Building: Educate sites on global procedures to build independent, high-functioning quality teams capable of maintaining long-term quality initiatives.

Knowledge/Skills/Competencies

• Quality Frameworks: Expert-level knowledge of ISO 13485, 21 CFR 820 (QMSR) and ANSI/ISO/ESD standards.
• NPI Quality Planning: Deep proficiency in defining critical quality business processes, tools, and system applications required to meet site-level and customer-specific quality objectives.
• Advanced Quality Tools: Mastery of core quality methodologies, including FMEA (Failure Mode and Effects Analysis), 8D Methodology, Change Control Board (CCB) protocols, and Manufacturing Quality Standards (MQS).
• Validation & DFx: Technical understanding of validation strategies (IQ/OQ/PQ) and Design for Excellence (DFx) to ensure seamless transitions from design to mass production.
• Performance Analytics: Ability to assess quality performance data to establish metrics, targets, and improvement strategies (e.g., Monthly Operations Reviews, Quality Excursion Reporting).

Typical Experience

15+ years of progressive experience in Quality Management, with a proven track record in NPI , manufacturing scale-up, and global QMS deployment.

Typical Education

• Bachelor's Degree or higher in Engineering, Quality Management or a related technical field.
• Industry certifications preferred (ASQ, Six Sigma, ISO13485 Lead Auditor, etc).

Notes

This job description is not intended to be an exhaustive list of all duties and responsibilities of the position. Employees are held accountable for all duties of the job. Job duties and the % of time identified for any function are subject to change at any time.

Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law).

At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them.

COMPANY OVERVIEW

Celestica (NYSE, TSX: CLS) enables the world's best brands. Through our recognized customer-centric approach, we partner with leading companies in Aerospace and Defense, Communications, Enterprise, HealthTech, Industrial, Capital Equipment and Energy to deliver solutions for their most complex challenges. As a leader in design, manufacturing, hardware platform and supply chain solutions, Celestica brings global expertise and insight at every stage of product development - from drawing board to full-scale production and after-market services for products from advanced medical devices, to highly engineered aviation systems, to next-generation hardware platform solutions for the Cloud. Headquartered in Toronto, with talented teams spanning 40+ locations in 13 countries across the Americas, Europe and Asia, we imagine, develop and deliver a better future with our customers.

Celestica would like to thank all applicants, however, only qualified applicants will be contacted.

Celestica does not accept unsolicited resumes from recruitment agencies or fee based recruitment services.