Gerente de Aseguramiento de Calidad de Laboratorio

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions).

• Bachelor's Degree in Life Sciences (Biology, Pharmacy, Biotechnology or related fields)
• Minimum 3-5 years of experience in a related field.
• Organized and able to manage time effectively.
• Ability to work within a highly regulated, labor intensive environment.
• Ability to understand, explain, follow, and enforce SOPs.
• Ability to plan, communicate and execute activities for the improvement of overall operations.
• Strong integrity and commitment to Quality and Compliance.
• Excellent oral and written communication skills to produce clear and concise factual findings.
• Advanced level of Spanish and English.
• This position requires significant travel and on-site presence in Egypt, with approximately 50% of the role based in Egypt.

It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.

Information about Grifols is available at www.grifols.com. If you are interested in joining our company and you have what it takes for such an exciting position, then don't hesitate to apply!

We look forward to receiving your application!

We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help.

Grifols is an equal opportunity employer.

To review and ensure that all procedures, testing methods and reports established in GEPD Plasma Testing Laboratories are in compliance to Egyptian regulations, and in accordance to cGMP, following Plasma Testing Specifications established and European Regulation. To manage and supervise Plasma Testing Laboratories Quality projects. To propose continuous improvement measures related to the quality systems of the Laboratories. To supervise the Quality Risk Management (QRM) process for the Laboratories.

• To review and ensure that all procedures established are in accordance to cGMP.
  • To supervise GEPD Plasma Testing Laboratories quality system and quality culture.
  • To ensure investigation for incidents are initiated, as well as root cause analysis are properly in place.
  • To participate and support internal and external regulatory inspections and audits performed in the Laboratories.
• To manage and supervise Plasma Testing Laboratories Quality projects.
  • Actively participate in Laboratory meetings for the follow-up of activities related to open Change Controls.
  • Coordinate the tasks required to be developed within the different areas of the company.
  • Review new procedures and processes to be implemented in the Laboratory under the scope of the Change Controls open.
• To ensure continuous improvement measures related to the quality systems of the Laboratories.
  • To supervise the monitoring of corrective and/or preventive actions implemented within the Laboratories. Ensure their proper implementation and effectiveness.
  • To monitor quality system indicators.
  • To propose improvements in the Laboratory's processes to enhance the quality system.
• To supervise the Quality Risk Management (QRM) process for the Laboratories.
  • To supervise Quality Risk assessment studies and reports, as well as coordinate mitigation tasks

Flexibility for U Program: Occasionally Remote.