About the Position

We are now looking for an experienced Validation Engineer with specialist competence in computerized systems for an initial consulting assignment with one of QRIOS Life Science's partners in Södertälje. The assignment starts as a parental leave cover but will transition into a permanent position with QRIOS with a 6-month probationary period.

This is your first assignment as a consultant with QRIOS Life Science – with very good opportunities for continued assignments and long-term development within our consulting network. As a consultant with us, you will have the chance to work in technically advanced environments, broaden your skills, and quickly build a strong professional network within Life Science.

QRIOS operates throughout the Mälardalen region (from Södertälje to Uppsala), Gothenburg, and Skåne. We always take into account where you want to work, and our assignments are geographically concentrated.

Start: Mid-February (flexible until mid-March for the right person)
Scope: Full-time
Employment type: Permanent with QRIOS (6-month probationary period)
Workplace: Södertälje with some possibility for remote work
Application deadline: January 22

Your Main Responsibilities

In this role, you will work with the validation of technically advanced laboratory instruments and associated computerized systems in a GMP-regulated environment. The assignment requires you to be self-sufficient from day one in validation methodology.

Plan, write, and execute validation protocols (IQ/OQ/PQ)
Ensure that computerized systems meet regulatory requirements and internal guidelines
Work according to GAMP 5, Data Integrity, and applicable GMP requirements
Collaborate with technical experts, QA, and the business
Document and report validation activities according to established quality processes

Who Are You?

You are an experienced validation engineer who thrives in complex technical environments and has the ability to quickly familiarize yourself with new systems. You appreciate clear requirements, a fast pace, and responsibility – and see the consulting role as an opportunity for both professional and personal development.

5+ years of experience in validation within Life Science
Very good knowledge of CSV and validation of computerized systems
Confident in working independently with IQ/OQ/PQ
Experience working in a GMP-regulated environment
Fluent in Swedish and English, both spoken and written

Desirable Qualifications

Experience with complex laboratory equipment or advanced automation solutions

About the Company

QRIOS is your reliable partner in the Life Science sector. We are experts in recruitment and consulting solutions for specialist and managerial roles within pharmaceuticals, medical technology, biotechnology, chemical engineering, and food technology. Our strength lies in the fact that our employees have extensive experience from the industry, which gives us a unique understanding of our clients' needs and challenges.

As a consultant with QRIOS, you will have the opportunity to try out different assignments, develop quickly, and build a broad network within Life Science. Together, we drive innovation and contribute to a better future.

QRIOS MINDS GO FURTHER.