Vacant job

Do you want to ensure quality within Life Science alongside some of the sharpest minds in the industry? Then this is where you belong. Here, you will find assignments that require curiosity, a solution-driven mindset, and sharp skills, giving you the chance to develop in new contexts. Together, we contribute to a better tomorrow and shape future solutions that make a difference for people and society.

You will become part of our business area Life Science Compliance and the Quality & Validation unit, which consists of 6 teams with broad expertise in quality, validation, and production.

As a consultant with us, you will work on varied assignments where you have the opportunity to quickly build experience and develop within several areas you are passionate about.

Examples of what you might work with:

• Validation, qualification, and commissioning of equipment, systems, and processes.
• Improving our customers' quality management systems.
• Improvement work within manufacturing and operational processes.
• Roles such as Quality or Process Engineer, Validation Engineer/Manager, or Sub-project Manager.

You have your own responsibility in your assignments, but never alone – you always have the support of a team with senior expertise to bounce ideas off.

We have offices in several locations in Sweden; this position is based at our office in Uppsala.

Here you get the best of the consulting role:

• Variety – different assignments, technologies, and businesses
• Rapid Development – a steep learning curve where you build both breadth and depth
• Impact – you drive improvement and quality for our customers

We are at the forefront of our field and work as advisory partners. This is evident in that we:

• Drive complex and developmental projects for our customers
• Train and lecture within our specialist areas
• Actively share knowledge – both internally and externally

With us, you always belong to a context – a team where we learn from each other and where senior colleagues contribute to your development.

You are curious, solution-oriented, and thrive in a role where you take responsibility and collaborate with others. You build trust, communicate clearly, and have a strong focus on quality.

We believe you have:

• At least 3 years of experience from GMP/GxP-regulated operations within Life Science
• A university or civil engineering degree in technology or natural sciences
• Experience in validation or technical production, preferably combined with a strong interest in quality and problem-solving
• The ability to work systematically and drive work forward
• Very good skills in Swedish and English

With us, you get something different.

We do not recruit for a specific assignment – we recruit to build our team long-term. This means we look at you, your competence, and your development over time, creating the right conditions for you to continue growing.

We work as advisory partners to our customers and value long-term relationships – both externally and internally. The team has a strong culture of knowledge sharing, where consultants learn from each other and contribute to the whole.

Our culture is something we are truly proud of. We are a Great Place to Work, year after year – and we see it as a testament to the environment we build together every day.

And yes – if our culture were in the walls, they would be soft.

During the summer period, it may take slightly longer before we can get back to you. Selection and interviews will begin as soon as we return from leave.

Apply today!

If you have questions about this position, please contact Helena Bomfim at 076-720 91 84 or [email protected].

Instead of applying for a specific position, please connect with us via our career page and indicate that you are interested in working as a sub-consultant – we will get in touch when a suitable opportunity arises.