Quality Assurance Specialist - Alphen aan den Rijn

Why Sakura?

When it comes to diagnosing cancer, there’s no time to waste!

At Sakura, we’re driven by our desire to advance cancer diagnosis through fully automated anatomic pathology and by providing our partners & patients with best-in-class innovations, quality and customer care.

What we do:

We empower pathology professionals all over the world by providing integrated solutions to deliver accurate & fast diagnoses of cancer, to optimize treatment success for each life we touch!

The opportunity:

We're seeking an experienced quality assurance specialist who will take responsibility of the overall compliance of Sakura Finetek Europe Quality Management System to the relevant ISO standards, while promoting a collaborative atmosphere of quality awareness and continuous improvement.

You report directly to the Manager RA&QA EMEAI.

Key responsibilities:

• Maintain and improve the Quality Management System (QMS) in accordance with relevant ISO standards.
  
• Drafting the quality assurance procedures.
• Conduct and supervise internal audits.
• Assisting in product and process risk management activities.
• Collect and compile statistical quality data.
• Analysing data to identify areas for improvement in the quality system.
• Monitor and drive corrective and preventive actions.
• Preparing reports to communicate the results of quality activities.
• Identify training needs and organize training to meet quality standards.
• Support on-site audits conducted by external providers.
• Evaluate audit findings and ensure appropriate corrective and preventive actions are implemented.
• Achieve personal and team objectives as outlined in the departmental plan.
• Support the release of (reworked) products from the supply chain.

We perfectly match if

you have

• a bachelor's degree.
• certifications as Quality Auditor, Quality Engineer, Quality Improvement Associate or Six Sigma are preferred.
• proven working experience in an international technical area- medical devices is a plus.
• at least 3 years of experience with ISO 13485.
• quality inspection, auditing and testing experience.
• experience with implementation of corrective action programs.
• Experience in change management.
• knowledge of tools, concepts and methodologies of QA.

and you

• have a good command of English & preferably Dutch.
• have a strong presentation, negotiation & communication skills.
• IT skills including Microsoft Office, QA applications and databases.
• connect easily & make an impact at all levels.
• are self-organised, structured and independent.
• have a pragmatic can-do attitude.

We offer you:

• an attractive salary package, including 8% holiday pay, a yearly bonus of max. 8%, a fully paid pension plan (according to the Dutch low), 29 paid holidays (full-time), hybrid working, laptop, a daily freshly prepared lunch and a gym discount.
• a great international collaborative work environment.

and last but not least, a great job opportunity where you have full ownership of your work, recognition of your achievements and professional development opportunities.

The invitation:

Our culture is friendly and open. We believe that the development of our people enables the company's growth.

Apply today & join:

• an inspiring community with a mission that matters! ''advancing cancer diagnostics''.
• our International organization who's leaded by a supportive & inspiring management.
• a financial healthy & privately owned company.

Acquisition in response to our job postings is not appreciated. This means that we think we can find a suitable colleague on our own.

*Please note that only candidates with valid EU work visa will be considered as viable candidates.