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Senior Healthcare Quality Engineer; m​/f​/d

Job in Westphalia, Prince George's County, Maryland, USA
Listing for: FedEx Group
Full Time position
Listed on 2026-02-01
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
Job Description & How to Apply Below
Position: Senior Healthcare Quality Engineer (m/f/d)
Location: Westphalia

We are looking for a seasoned Healthcare Quality Engineer with deep expertise in pharmaceutical logistics and cold chain operations to ensure compliance with global regulatory and industry standards. The ideal candidate will have experience supporting CEIV Pharma-certified operations, applying WHO PQS standards, and conducting temperature mapping and validation activities across transportation and storage environments.

Who we are:

Fed Ex is the largest express transportation company in the world, connecting more than 220 countries and territories. We work every moment to deliver the most important package of someone’s day. Our team of passionate people know their day-to-day work is invaluable in delivering outstanding experience to our customers. 530,000 team members strong, we are as diverse as the world we serve.

We love what we do, and we do it well. Our reach is big, and so are our dreams. Join us and let's write our next chapter together.

What you will be doing:

  • Support and maintain the Quality Management System (QMS) to meet GDP, CEIV Pharma, and ISO 9001 standards for pharmaceutical transport and cold chain logistics.

  • Lead or support temperature mapping and validation of cold chain lanes, vehicles, packaging systems, and storage areas in alignment with WHO PQS and regulatory expectations.

  • Analyze and respond to temperature excursions and deviations, performing structured root cause analysis and implementing effective CAPAs.

  • Prepare and maintain validation protocols, reports, and mapping records for audits and client reviews.

  • Participate in CEIV Pharma audits, ensuring ongoing compliance and alignment with IATA standards for pharmaceutical air freight.

  • Conduct vendor and carrier qualification audits, including risk assessments, technical evaluations, and QTA development.

  • Interpret and apply WHO Performance, Quality and Safety (PQS) guidelines for equipment and process control in global health supply chains.

  • Collaborate cross-functionally to implement risk-based controls, corrective actions, and improvements to cold chain operations.

  • Generate and manage controlled documentation, including SOPs, work instructions, deviation reports, and training guides.

  • Deliver training and coaching to operations staff on temperature-sensitive handling, GDP requirements, and audit preparedness.

  • Design, implement, and optimize processes for pharmaceutical clients, with a focus on temperature-sensitive products and regulatory compliance.

  • Conduct process mapping, time studies, and data analysis to identify inefficiencies and recommend improvements. PFMEA,

  • Support customer onboarding and solution design, including RFQ responses, SOP development, and KPI definition.

  • Collaborate with Quality, Operations, and IT teams to implement process improvements.

  • Perform root cause analysis and corrective action planning related to cold chain excursions or supply disruptions.

  • Stay up-to-date with pharmaceutical regulations, CEIV Pharma, WHO PQS, and other applicable industry standards.

  • Provide technical leadership during customer audits and continuous improvement initiatives.

What do you bring with you:

  • Bachelor’s degree in Engineering, Pharmaceutical Sciences, Logistics, or a related technical discipline.

  • 5+ years of experience in pharmaceutical cold chain logistics, GDP compliance, or regulated quality systems.

  • Demonstrated experience with CEIV Pharma certification requirements and audit processes.

  • Knowledge of WHO PQS standards, particularly as they apply to cold chain equipment and procedures.

  • Strong technical understanding of temperature mapping, validation protocols, and cold chain risk mitigation.

  • Skilled in quality tools and methodologies: CAPA, RCA, 5 Whys, 8D, FMEA.

  • Excellent written and verbal communication skills, with the ability to interface with internal teams, clients, and regulatory auditors.

  • Mandatory Fluent English and German language.

Preferred Qualifications:

  • Certifications:

    GDP, ISO 9001 Lead Auditor, ASQ CQE, or CEIV Pharma-trained.

  • Experience working with global health organizations, vaccines, or biologic product distribution.

  • Familiarity with QMS platforms, data loggers, IoT-enabled temperature monitoring systems, and thermal…

Position Requirements
10+ Years work experience
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