Vacant job

Job Description

Laboratory Engineer specializing in Validation and Qualification (GxP).

Are you looking for a challenging consulting assignment starting after the summer, where your expertise in validation and quality makes a real difference? On behalf of a client, we are now seeking a structured and analytical Laboratory Engineer for an exciting role at an analytical laboratory.

About the Role

In this consulting role, you will support the business with the planning, execution, and documentation of validation and qualification activities in accordance with current regulatory requirements (GxP). Your main focus will be on the qualification of equipment and systems, as well as conducting risk assessments.

Scope: Full-time, consulting assignment for 6 months.

Start Date: After summer 2026.

Location: Flexible/Hybrid (possibility for some remote work, but parts of the assignment require presence at the analytical laboratory).

This is a consulting assignment via Randstad Life Sciences. Randstad Life Sciences specializes in Life Science competencies. As a consultant with us, you will receive a market-competitive salary, benefits, and a collective agreement. Your consulting manager is always there for you and ensures you receive varied and developmental assignments at different companies across various industries. At Randstad Life Sciences, your personal development is the focus, and you are offered a large network as well as many social activities.

Responsibilities

Your Main Tasks

• Plan, execute, and document validation and qualification activities.
• Focus on the qualification of laboratory equipment and systems.
• Conduct risk analyses and risk assessments.
• Ensure that work is carried out in accordance with current regulatory requirements (GxP).

Who are we looking for?

To succeed in this role, we require a relevant university degree in chemistry, pharmacy, biotechnology, or similar. You have extensive experience with validation in a laboratory environment, as well as qualification (IQ/OQ/PQ) and risk analyses. You are accustomed to working in a quality-controlled environment within the pharmaceutical or medical technology sector (GMP, GLP, ISO13485).

Desirable qualifications:

• Experience with analysis using chromatography systems (GC, GC headspace, HPLC).
• Good understanding of computerized systems.

Language Requirements:

• Good knowledge of both Swedish and English, in both spoken and written form, is required.

Does this sound like your next assignment?

Apply today! Selection and interviews are conducted on an ongoing basis.

Qualifications

Personal Attributes

We place great emphasis on your personal attributes. As a person, you are structured and meticulous in your work, which is a prerequisite for handling documentation and regulatory requirements. You are analytical with strong problem-solving skills and thrive working independently and driving your processes forward.

About the Company

Randstad

At Randstad, we know that every person has a place in the labor market. With operations throughout the country and across all competency areas, we help people find a job that feels right, where they have the opportunity to grow, develop, and achieve their full potential.

With nearly 600,000 employees in 38 countries, Randstad is a world leader in HR services, with the goal of becoming the world's leading and most appreciated partner in the labor market. By combining our passion for people with the power of today's technology, we help people and companies achieve their full potential. We call it Human Forward.