Associate Director, Medical Device & Combination Product Quality Assurance
Heist op den Berg, Antwerp, Belgium, Oss
5 dagen geleden


The Associate Director, MedicalDevice & Combination Product Quality Assurance reports to the Director of MedialDevice and Combination Product Quality (MDCPQ) and is responsible forindependent compliance support of Medical Devices including the deviceconstituent part of Combination Products.

This position will interact withcross functional teams working with all levels of employees. Activities willinclude developing, documenting, and maintenance of technical businesssolutions or audits of data, policies, procedures, and systems to ensurecompliance with Medical Device (21CFR 820s) and Combination Product currentGood Manufacturing ruling (21CRFT part 4.

Device Risk Management (ISO 14971)and other worldwide regulations and MSD Requirements.

The primary purpose of this position is to provide Device Quality Assurancesupport and leadership to ensure sustaining / remediation activities andsuccessful quality oversight of prospective combination products.

The AssociateDirector will be expected to apply his / her knowledge of product development,design control principles, risk management and quality engineering techniquesto positively influence commercial and new product launches to ensure they aredeveloped and manufactured in accordance with regulatory, company, and customerrequirements.

The Associate Director will review and evaluate scientific andtechnical data as it pertains to product and product testing and lead teams toidentify and solve complex problems.

This individual will :

  • Actively represent DeviceDesign Quality function on commercial and product / core development teamssupporting quality issues related to medical devices or the device constituentof a combination product.
  • Review and approve DesignControl and Device Risk Management documentation for regulatory filings,clinical supply, development and design transfers qualification.
  • Evaluatedeficiencies and assess impact on compliance status.

  • Contribute todeveloping / revising policy and procedures for Medical Device and Combination ProductQuality and / or supported areas.
  • Remain informed of industrytrends as described in worldwide regulations and industry standards.
  • Provide guidance to our manufacturing divisions and ourresearch labs device functions and other personnel to ensure end to end Qualityby Design, Six Sigma, Reliability, and Design Control principals areimplemented effectively.
  • Participate in design reviews,CAPA reviews, and ad-hoc technical reviews of combination products.
  • Be a hands-on participant inall stages of combination product development including but not limited tooversight of purchasing controls and supplier quality.
  • Work with external partners todevelop products.
  • Author retrospective designcontrol documentation that encompasses the life cycle and risk-based approachof development and sustaining activities.
  • Reports to ensure that thetesting is sufficient to meet regulatory requirements and quality objectives.
  • Provide input to design andmanufacturing documentation including material specifications, drawings,inspection procedures, and manufacturing procedures, to ensure that theresulting products can be adequately manufactured and tested.
  • Facilitate translation of vaguecustomer needs into critical to quality and design inputs / output requirements,including but not limited to chemical, physical, and performancespecifications.
  • Solliciteren
    Bij de favorieten invoegen
    Verwijder van favorieten
    Mijn E-mail
    Door op "voortzetten" te klikken, gaat u ermee akkoord dat neuvoo uw persoonlijke gegevens verzamelt en verwerkt die u in dit formulier hebt verstrekt, om een ​​neuvoo-account te maken en u te abonneren op onze e-mailwaarschuwingen, in overeenstemming met ons Privacybeleid . U kunt uw toestemming te allen tijde intrekken door te volgen deze stappen .