My client is a leading engineering company in the Pharma industry, and for them I am currently looking for 2 Quality QA/QCV Engineers (m/f/x)- who can support immediately on-site in Denmark in their on-going project.
Framework:
Start: latest by 23rd of March 2026
Capacity: 100%
Length of contract: until end of September extensions
Client location: Kalundborg, Denmak
Workplace: 100% on-site at customer location
Project phase: acceptance phase/commissioning
Contract: Freelance
Main tasks:
Prepare GDP-compliant documentation ( test packages, pressure test reports, personnel certificates, measurement certificates, weld documentation, pressure tests, plant cleaning, test packs, SAT documentation)
Train the line walkers and turnover staff and review the documentation they return.
Direct communication with the customer is key-aspect of this role, including analyse of documentation together with the customer and discussing the topics that must be reviewed or modified.
Requirements:
Possibility to work fully on-site for the contract length in Denmark.
Fluency in English is a must- fluency in Danish as nice to have but is not mandatory for this role.
Senior experience in Quality, Qualification and Validation in pharma engineering plants (+ 5 years)
Deep knowledge of GDP/GMP Documentation.
If you are qualified for the role and ready to take the next challenging project in Denmark, do not hesitate to send your updated cv (only in English) and your hourly rate for on-site work (all travel costs inclusive, in Euros) to:
I will review the applications and if there is a good fit to my client's requirements, I will call you via phone to discuss further details.
Kind regards,
Julia
Desired Skills and Experience
Pharmaceutical, Life science, plant engineering, Pharma, QA, Quality Assurance, Quality engineer, QVC, validation, commissioning quality, GDP, GMP, Plant quality engineer
SThree_Germany is acting as an Employment Business in relation to this vacancy.