Vacant job

Mpya Sci & Tech was created by and for people who love technology and science. We’re not here to do what everyone else is doing. We believe that real talent lies in individuals who dare to keep growing throughout their entire lives. With extensive experience and deep industry knowledge, we’ve built a forward-leaning and cutting-edge company—our way. At Mpya Sci & Tech, we believe in a sustainable working life where we build a culture together based on genuine involvement, eager curiosity, and the freedom to be yourself. Learn more at: www.mpyascitech.com.

Quality is rarely noticed when everything works. But it is noticed immediately when something doesn’t.

Behind stable processes, reliable systems, and safe production are people who see the details, understand the requirements, and know how quality is built in practice.

We are now looking for you who want to work as a Validation Engineer and Consultant within the pharmaceutical and medtech industry – where technology, quality, and problem-solving meet every day.

⚡ Why consultants thrive with us

At Mpya Sci & Tech, we combine specialist competence with a human and long-term consulting career. Here you get the opportunity to work in varied assignments in the industry – without losing your sense of belonging to a team that understands your daily life.

We believe in freedom under responsibility, close leadership, and that the right people make the biggest difference when given the right conditions. Therefore, we place great importance on matching assignments based on both competence and motivation.

With us, you become part of a network where knowledge exchange, collaboration, and development are a natural part of everyday life.

⚙️ What does the role involve?

As a Validation Engineer, you work on assignments where quality and regulatory compliance are central. Depending on the assignment, you can contribute within:

• IQ/OQ/PQ and qualification of equipment, processes, and facilities
• Validation planning and strategies
• Risk analysis and requirement specification
• Change control and design control
• CSV and computerized systems
• Improvement work and standardization

🧩 Who do we think you are?

You thrive in environments where structure and quality are important, but where flexibility, collaboration, and the ability to find forward-looking solutions are also required.

You are accustomed to working in regulated environments and feel confident taking responsibility, driving your work, and quickly getting up to speed in new contexts. At the same time, you are communicative and build trust through a professional and non-hierarchical approach.

📌 To succeed in the role, we see that you have:

• An academic education in fields such as biotechnology, medical technology, chemical engineering, or equivalent work experience.
• Several years of experience in validation/qualification (IQ/OQ/PQ).
• Experience from GMP-regulated operations and/or ISO 13485.
• Good communication skills in Swedish and English.

💬 Curious about the next step?

This is a proactive advertisement for upcoming assignments. We meet candidates continuously and are happy to have a dialogue about what you are looking for and how we can match it. Are you curious about the role or the consulting life with us? Reach out and let’s talk further.

We look forward to getting to know you!