Quality Assurance Professional

2 weken geleden


Eindhoven, Noord-Brabant, Nederland Yacht Voltijd
{"Functieomschrijving

Product Reliability Specialist

As a Product Reliability Specialist, you will play a pivotal role in achieving high-quality performance, ensuring compliance, and fostering sustainability in our factory operations. You will drive continuous quality improvement across all phases of the manufacturing lifecycle, including overseeing products, parts, and services, and managing sustaining change throughout production.

Responsibilities:

  • Ensure Product Quality: Oversee product quality and ensure full compliance, contributing to manufacturing excellence.
  • Drive Product Reliability: Facilitate timely releases of products, ensuring high quality and reliability.
  • Collaborate Cross-Functionally: Work closely with Quality Engineers and Reject Handlers, acting as the primary point of contact for specific modalities, customers, and key stakeholders such as the legal manufacturer and operations manager.
  • Lead Cross-Functional Partnerships: Strengthen collaboration between multiple stakeholders, supporting cross-functional partnership efforts.
  • Support Change Management: Guide and assist in change management processes related to manufacturing and control adjustments.
  • Analyze Nonconformances: Assess defects, manage nonconformance (NC) processes, and determine appropriate dispositions for quality issues.
  • Monitor Operations Performance: Contribute to monitoring, reporting, and driving improvements in operational performance, assisting with improvement programs within the factory.
  • Manage Supplier Quality: Collaborate with Supplier Quality teams to investigate and resolve issues, managing Factory Holds and providing regular status updates.

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Requirements:
  • Experience: Minimum of 2 years in quality engineering within an operational environment, preferably in medical devices, pharmaceuticals, automotive, or aerospace industries.
  • Education: Bachelor's degree or higher, ideally with a technical background.
  • Regulatory Knowledge: Familiarity with Medical Device Regulations and standards such as FDA CFR and ISO 13485:2016 is highly preferred.
  • Language Skills: Proficiency in English is required; Dutch is a plus.
  • Coordination Skills: Prior experience coordinating quality-related tasks and initiatives is advantageous.

We welcome candidates from a range of experience levels—junior, medior, and senior. If you're ready to advance quality standards in a collaborative and challenging environment, we encourage you to apply.

Arbeidsvoorwaarden

Primary employment conditions

· A good salary as per market standards.

· 8.33% holiday pay calculated over 12 monthly salaries.

Secondary employment conditions

· Pension Plus scheme (build-up from day 1);

· Net €750 to set up your home workplace;

· 13th month (paid periodically on a pro-rata basis) or the possibility of a bonus (4 to 8% per quarter - average of 1 month's salary per year);

· 25 days of vacation per year based on 40 hours;

· Travel expenses reimbursement;

· Options for working from home with a home work allowance;

· Yacht Academy with a training budget of up to €3,500 per year;

· Referral bonuses up to €1,500;

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