Cantel Medical

QA Specialist

IT-Pomezia
Job ID
2017-3498
# Positions
1
Category
Quality / Regulatory
Cantel Italy

Company Overview

Cantel Medical is a leading global company dedicated to delivering innovative infection prevention and control products and services for patients, caregivers, and other healthcare providers, which improve outcomes, enhance safety and help save lives.  Our products include specialized medical device reprocessing systems for endoscopy and renal dialysis, advanced water purification equipment, sterilants, disinfectants and cleaners, sterility assurance monitoring products for hospitals and dental clinics, disposable infection control products primarily for dental and GI endoscopy markets, dialysate concentrates, hollow fiber membrane filtration and separation products. Additionally, we provide technical service for our products. 

Job Overview

Provide quality assurance support to Manufacturing Operations by resolving quality related issues, improving product quality and investigating customer complaints.
Utilize the Correction and Preventive Action system to pursue continuous improvement of the Quality System and Cantel Medical products. Prepare and maintain accurate audit working papers and files to support audit findings

Main Responsibilities

  • Manage NC’s process for Chemistry products and EM machines (including support to management of raw materials/components issues raised in Incoming and Production areas).
  • Support CAPA’s process and follow-up on corrective actions to ensure that they are implemented on time and are effective.
  • Ensure product complaints are promptly investigated and, where needed, adequate corrective/preventive actions are accordingly raised and implemented.
  • Participation on demand in preparation of PFMEAs.
  • Evaluate opportunities for improvements to the operation of the QA department.
  • Support periodic review of department internal control procedures.
  • Where necessary, gather and trend quality data for periodic review and Quality Management Reviews.
  • Support the QA Manager for internal and external audits activities.
  • Assist the QA Manager in developing the corrective action plans for any findings resulting from internal and external audits.
  • Ensure that personal training records are maintained in conjunction with HR department.

Qualifications

 

  • Master degree in Life Sciences.
  • Knowledge of GMP requirements.
  • Experience in audit activities.
  • Good interpersonal and professional communication skills.
  • Minimum of one to three years related experience required.
  • Ability to work from designated office for collaborative/interactive fulfillment of duties.
  • Flexibility and resilience in the face of constraints, frustrations or adversity.
  • Appropriately and directly interact with other staff members and/or outside associates.
  • Operate office equipment such as computer and telephone.
  • Attend and participate in meetings via phone, computer, or in person.

Minimum Qualifications

 

 

Preferred Qualifications

 

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