Drug Product Delivery Operator

Hays AB / Laborantjobb / Göteborg
2026-02-25


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Drug Product Delivery Operator - Consultancy Assignment in Gothenburg

Are you motivated by structure, precision and contributing to life-changing clinical research? We're looking for a detail-oriented DPD Operator to support a global biopharmaceutical company committed to advancing innovative medicines. This is a unique chance to be part of a highly regulated, science-driven environment where your work will directly support clinical trials across the world.

What you will be working with

In the Drug Product Delivery (DPD) function, you will be involved in the end-to-end handling of investigational medicinal products. Your tasks play a central role in ensuring that clinical trial materials reach patients safely, correctly and on time.

You will be part of a team specialising in:

* Material Management
* Packing & Labelling
* Distribution of investigational medicinal products

This is a hands-on operational role where accuracy, documentation and compliance are essential.

Your core responsibilities:

* Receiving, handling and packing investigational medicinal products
* Ensuring full traceability of items, batches, packaging materials and labels
* Preparing and reviewing GMP-compliant documentation
* Acting as a point of contact for distribution-related study questions
* Maintaining equipment and facilities according to GMP standards
* Supporting improvement initiatives and deviation management
* Contributing to the development of internal procedures within GMP and SHE

Who we are looking for

This role suits someone who thrives in structured environments and enjoys working within established quality systems. You are analytical, solution-oriented and able to work independently while being a reliable team contributor.

Essential qualifications:

* BSc/MSc in chemistry, pharmacy, engineering, logistics or similar
* Approximately 2 years' experience in pharmaceutical development or related field
* Comfortable working in a regulated GMP environment
* Strong communication skills in English
* Experience working in complex, multicultural environments

Beneficial skills:

* Understanding of SHE and GMP requirements in R&D or manufacturing
* Knowledge of supply chain processes within pharma
* Familiarity with clinical trial materials and distribution standards

What you can expect

You will join a highly collaborative team passionate about delivering high-quality clinical trial materials. The environment is fast-paced and dynamic, offering great opportunities to grow your skills within pharmaceutical operations and regulatory frameworks.

Ready for your next step?

If this sounds like the right challenge for you, click "Apply now" to submit your CV or get in touch with us directly to learn more.

If this particular role isn't the perfect match, feel free to contact us for a confidential career discussion.

About Hays

At Hays, we connect talented professionals with opportunities that help them grow, thrive and make an impact. With deep industry expertise and a global network, we support organisations in finding the right skills - and help candidates discover roles aligned with their ambitions.

Our purpose is simple: to empower people and organisations to succeed. Whether you're seeking your next challenge or looking to strengthen your team, Hays is here to support you every step of the way.

Ersättning
Not Specified

Så ansöker du
Sista dag att ansöka är 2026-03-07
E-post: Hays.47195.3101@haysse.aplitrak.com

Arbetsgivarens referens
Arbetsgivarens referens för detta jobb är "900839".

Omfattning
Detta är ett heltidsjobb.

Arbetsgivare
Hays AB (org.nr 556640-6103)

Kontakt
Linnea Killander
linnea.killander1@hays.com
+46 8 588 043 00

Jobbnummer
9763229

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