Job Openings

Position Summary

• Location: Cairo, Egypt
• Department: MedTech TCT
• Reporting to : Regional Director

Job Purpose:

Act as a hands-on Service Engineer responsible for the installation, commissioning, maintenance, and troubleshooting of TCT equipment across the Middle East. This role serves as the primary field representative for TCT, ensuring equipment reliability, timely issue resolution, and an excellent customer experience.

Responsibilities / Duties:

Key Responsibilities

1. Install, commission, calibrate, and maintain equipment at customer sites across MEA.
2. Diagnose and resolve hardware and software issues, both onsite and remotely.
3. Execute preventive maintenance and performance checks and document findings.
4. Prepare detailed service reports, including root cause, actions taken, parts used, and recommendations.
5. Train customers, partners, and internal teams on safe operation and best practices.
6. Manage spare parts, RMA, and service tickets according to SLA requirements.
7. Collaborate with Sales and Product Management on escalations and service improvement plans.
8. Always uphold EHS standards and site compliance requirements.
9. Perform other duties as assigned.
10. Report Adverse Drug Reactions (ADRs) and complaints about Fresenius Kabi products from Market Unit MENA to the responsible function at mena.vigilance@fresenius-kabi.com immediately after receipt, and no later than within 1 business day

Competence Requirements:

• Bachelor’s degree in Electrical, Mechatronics, Mechanical, or Electronics Engineering.
• 3–8 years of experience in Field or Service Engineering, including installations, commissioning, and diagnostics.
• Strong troubleshooting mindset with the ability to work effectively under time pressure.
• Fluency in English and Arabic is required. French language skills are preferred.
• Valid passport and willingness to travel 50–70% across the GCC, Levant, and North Africa.
• Familiarity with service documentation, including ISO/OEM standards, ticketing tools, and basic reporting tools such as Excel and Word.
• Prior experience in the healthcare or pharmaceutical industry is preferred.

Required Skills:

• OEM experience, including install base ownership and warranty/after-warranty service.
• Experience in one or more of the following areas: industrial automation, instrumentation, power systems, BMS/HVAC, healthcare/biomedical equipment, oil and gas, or high-tech equipment.
• Vendor certifications such as Siemens, ABB, Schneider, or Honeywell are preferred.

to apply click here

Position Summary

• Legal Entity: Fresenius Kabi Saudi Arabia / MENA Region
• Location: Riyadh, Saudi Arabia
• Department: Regulatory Affairs & Quality Assurance – MENA Region
• Reporting to : Head of Regulatory Affairs & Quality Assurance - MENA Region

Job Purpose:

The Regulatory Affairs Associate supports Regulatory Affairs activities across the MENA region, with primary focus on Saudi Arabia. This junior role supports regulatory submissions, maintenance of product registrations, and compliance with local Health Authority requirements. The position contributes to ensuring timely approvals and lifecycle management of products under supervision of Head of  Regulatory Affairs & Quality assurance.

Responsibilities / Duties:

Key Responsibilities

• 1.    Support preparation, compilation, and submission of regulatory dossiers (new registrations, variations, renewals) for Saudi Arabia and MENA countries.

  2.    Assist in tracking submission timelines, approvals, and regulatory commitments.

  3.    Support lifecycle management activities for registered products.

  4.    Maintain and update regulatory databases and trackers (e.g., submission status, HA queries).

  5.    Liaise with internal , Regional & global stakeholders (Quality, Pharmacovigilance, Supply Chain, Commercial) to collect required regulatory documents.

  6.    Support responses to Health Authority queries under guidance of senior RA staff.

  7.    Ensure regulatory documents are archived in compliance with internal procedures and eDMS requirements.

  8.    Support implementation of regional regulatory projects and digitalization initiatives.

  9.    Performs other duties as assigned

   

  Reporting & Compliance

  Report Adverse Drug Reactions (ADRs) and Complaints about Fresenius Kabi’s products from Market Unit MENA to the responsible function, i.e., mena.vigilance@fresenius-kabi.com, immediately after receipt, but latest within 1 business day.

Competence Requirements:

• Bachelor’s degree in Pharmacy.
• Saudi National with 1–2 years of experience in Regulatory Affairs, preferably within Multinational company
• Understanding of Saudi FDA (SFDA) regulatory requirements is a must.
• Experience in regulatory documentation and submission processes In other MENA countries.

Required Skills:

• Strong attention to detail and good organizational skills.
• High level of integrity and ability to maintain confidentiality
• Good written and verbal communication skills.
• Ability to work collaboratively in a cross-functional and multicultural environment.
• Basic MS Office proficiency (Word, Excel, PowerPoint).
• Ability to manage multiple tasks and meet deadlines.
• Willingness to learn and develop regulatory expetise.
• High level of integrity and ability to maintain confidentiality.

to apply click here