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QA Leader - Africa at GE Healthcare

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Company Details
Industry: Pharmaceuticals
Description: GE Healthcare provides transformational medical technologies and services that are shaping a new age of patient care. Our broad expertise in medical imaging and information technologies, medical diagnostics, patient monitoring systems, drug discovery, biopharmaceutical manufacturing technologies, performance improvement and performance solutions services help our customers to deliver better care to more people around the world at a lower cost. In addition, we partner with healthcare leaders, striving to leverage the global policy change necessary to implement a successful shift to sustainable healthcare systems. Our "healthymagination" vision for the future invites the world to join us on our journey as we continuously develop innovations focused on reducing costs, increasing access and improving quality around the world. Headquartered in Chicago, IL, GE Healthcare is a unit of General Electric Company (NYSE: GE). Worldwide, GE Healthcare employees are committed to serving healthcare professionals and their p
Job Description

The Quality Assurance Leader is responsible for the zone’s compliance to GEHC QMS and the local regulatory requirements. She/he is responsible for the quality management system, controls and continuous improvement and establishing best practice standards to assure product safety and quality.

Key responsibilities include:

Participate in the development and maintenance of the region Quality Management System (QMS) and relevant processes to assure product quality and safety.

Ensure company procedures and proper documentation practices are followed per GE Healthcare QMS requirements

Attend region/zone QMS and metrics reviews with service and business management functions

Coach and mentor functional teams on the development, maintenance and implementation of local procedures (if any)

Provide advice & counsel the business managers in the zone with QMS related processes

Assist the Quality Assurance Site Manager (when applicable) in preparation for internal/external audits and implementation of corrective actions to address non-conformities.

Work closely with other functional areas (e.g. Marketing, Engineering, Service) to ensure compliance to applicable regulations

Lead and support continuous improvement activities assigned, which may include such areas as: ISO standards compliance, Risk management, and metrics development/implementation.

Qualifications:

  • Bachelor's degree in Engineering, Medical Device Technology or Scientific Field 
  • Experience and understanding of product development, manufacturing, quality control and servicing in the medical equipment or pharmaceutical industry 
  • Knowledge and experience with ISO9001 and 13485, and/or other international quality systems requirements
  • Proven track record in performing external and internal audits preferred.  
  • Ability to read, analyze and interpret business plans, technical procedures and governmental regulations 
  • Strong computer skills
  • Ability to communicate fluently in English
  • Front line operational responsibility in Field Service but also support technology transfer projects, guide/support sourcing for compliant purchases and support supplier quality initiatives where necessary
Salary: Discuss During Interview
Education: Diploma
Employment Type: Full Time

Key Skills

manufacturing 
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