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Specialist Global Distribution QA

Specialist Global Distribution QA

Specialist Global Distribution QA

Specialist Global Distribution QA

Abbott GmbH

Medizintechnik

Basel

  • Art der Beschäftigung: Vollzeit
  • Vor Ort

Specialist Global Distribution QA

Über diesen Job

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.

Abbott Established Pharmaceutical Division (EPD) is looking for a

Specialist Global Distribution QA

for its global Pharma Division Headquarter based in Allschwil- Basel.

( This is a fixed-term, one-year assignment offered via a third-party vendor .)

Are you passionate about quality and compliance in pharmaceutical distribution? Do you thrive in a dynamic, cross-functional environment? If so, this role could be your next career move!

What You’ll Do:

As a key member of our Quality team, you’ll ensure our Allschwil site maintains its Pharmaceutical License and GDP authorization, while supporting the safe and compliant distribution of medicinal products, nutritional items, cosmetics, and medical devices across global markets.

Your responsibilities will include:

  • Maintaining and improving the site’sQuality System(training, documentation, change control, deviations, audits)

  • Managingcomplaints, returns, and supportingmarket actions

  • Qualifying and monitoringlogistics and distribution partners

  • Ensuringcustomer verificationand maintaining theApproved Supplier List

  • Providing QA input intoglobal distribution projects, including:

    • Counterfeit prevention

    • Temperature monitoring and excursion management

    • Product transportation optimization

    • Serialization and aggregation

    • Supply chain validation

    • Material listing approvals

You’ll collaborate closely with teams acrossSupply Chain, Global QA, Master Data, and Product Protectionto ensure compliance with GxP standards.

What You Bring:

  • A degree inPharmacy, Chemistry, Biology, Microbiology, Engineering, or a related scientific field

  • At least1 year of experiencein QA or operations within a pharmaceutical setting

  • Solid understanding ofEU GMP/GDPand international standards (PIC/S, WHO, ICH)

  • Strong problem-solving and communication skills

  • A collaborative mindset and ability to work cross-functionally

  • FluentEnglish(additional languages are a plus)

  • Willingness to travel within Europe (approx. 10%)

Why Join Us?

At Abbott, you’ll be part of a global team that’s committed to improving lives through innovation and quality. You’ll work in a supportive, fast-paced environment where your contributions truly matter.

If this sounds like the right opportunity for you, we’d love to hear from you. Please submit your CV (PDF format preferred). We welcome applicants from all backgrounds and are committed to building a diverse and inclusive team.

(If you want to upload several documents, don`t save in between uploading them to be able to do so. Once you save your uploads, you will not be able to add more documents)

Unternehmens-Details

company logo

Abbott GmbH

Medizintechnik

10.001 oder mehr Mitarbeitende

Wiesbaden, Deutschland

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