Do you have experience in quality assurance/regulatory affairs in a medical device & diagnostics industry?

Do you feel deeply motivated at the right job when your role best fits your aspirations and values? If so, then read on!

Our client is a leading supply chain company aiming to offer innovative approaches to improve health and wellbeing around the world! They’re looking to hire a Product Quality Assurance Officer to support them and share the organization’s values.

Responsibilities:

  • Manage and maintain product dossiers or technical documentation submitted as part of client’s product prequalification process.
  • Support operational units in defining product eligibility and quality requirements and corresponding QA documentation, specifically for medical devices and diagnostics.
  • Liaise with Strategic Supply Chain and Client Service Units to ensure completeness and accuracy of product dossiers received from vendors, as part of RFQ/RFP process.
  • Compile and complete initial screening of product dossiers to make any required recommendations for their approval to the QA and Regulatory Manager.
  • Ensure proper filing, access, and retrieval of product dossiers and records related to QA decisions.
  • Track the Global Fund’s eligible list of diagnostics on a weekly basis and coordinate with the Product QA Data Officer to ensure that only approved products are maintained in PFSCM item master in the ERP system.
  • Centralize product QA requirements in a relevant tool/platform to serve as a quick reference for operational units.
  • Collaborate with Strategic Sourcing to streamline catalogue management by contributing insights from medical devices and diagnostics regulations.
  • Monitor field safety notices (FSN) and field safety corrective actions (FSCA) issued by manufacturers and liaise with suppliers and internal units to ensure required actions are completed.
  • Support Logistics and 4PL Units in shipment planning and ensuring compliance with local regulatory requirements by providing insights on product characteristics, stability profile and storage requirements.
  • Summarize and verify shipment/data logger reports under the supervision of the QA and Regulatory Manager, notify Logistics Unit on the disposition of the delivered goods.
  • Support QA-related incidents by gathering information, providing input for investigation and contributing to the resolution.
  • Support QMU by preparing reports on incidents that communicate status, trends and outstanding actions for management review, project management, and KPI reporting to the client.
  • Assist in the development and revision of QAU-related Standard Operating Procedures and Work Instructions in line with client’s Quality Management System.

Requirements:

  • Bachelor’s degree in Healthcare and Life Sciences or other relevant field.
  • 3+ years’ work experience in quality assurance/regulatory affairs in a medical device & diagnostics industry, healthcare organization.
  • Knowledge about Good Manufacturing Practices, Good Distribution Practices, ISO 13485, and other relevant standards.
  • Understanding of the medical device & diagnostics regulatory environment both at international and country level.
  • Knowledge of the international health products market with specific reference to essential diagnostics required for COVID-19, HIV/AIDS, Tuberculosis, and Malaria.
  • Strong interpersonal skills and an ability to work across disciplines and in diverse locations internationally.
  • Ability to work comfortably with Microsoft Office software, specifically Word, Excel, and PowerPoint. Advanced user level of Excel preferred.
  • Excellent written/verbal communication and interpersonal skills with strong sense of customer service. English fluency required, including speaking, writing, understanding, and reading.
  • Demonstrated analytical skills; solution oriented with a high sense of quality, attention to detail, accuracy, efficiency, and meeting tight deadlines.
  • Team player who is also able to work independently and handle conflicting priorities while maintaining consistent, quality performance standards.
  • Willingness and availability to travel, and perform other duties as needed.
  • Must be authorized to work in the Netherlands.

Ready for this new challenge? Apply now and let’s get in touch!

Octagon Professionals International is a full-service recruitment and HR services firm with 30 years of experience in the European and international market. Our large network of professionals across multiple functional areas, and multi-national team provide flexible solutions customized to individual client needs.

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Job Information

Job Reference: BBBH2252_1641402320
Salary:
Salary From: £
Salary To: £
Job Industries: Life Sciences & Pharmaceuticals
Job Locations: Utrecht area
Job Types: Permanent
Job Skills: quality assurance, healthcare, medical devices , regulatory affairs, ISO 13485

Apply now


Octagon Recruitment

Recruitment Team

+31 (0)70 324 9300