Vacant job

Do you want to help ensure quality in Life Science together with the sharpest minds in the industry? Then this is where you should be.

With us, exciting assignments await that thrill the stomach – assignments that require curiosity, analytical ability, and a desire to find solutions. The variation in our projects means that you will constantly develop and put your skills to the test in new contexts. At the same time, you will contribute to something greater.

Through our work, we help shape tomorrow's solutions – we make a difference for people, society, and the future. We do all this together, in teams filled with some of the industry's sharpest and most experienced colleagues. Here, we inspire each other, generously share knowledge, and drive development forward – with quality, curiosity, and sharpness as our common foundation.

This will be your role

We are looking for a consultant for the Life Science Compliance business area and the Quality & Validation unit. The unit consists of about 70 consultants distributed across six teams. With a broad spectrum of skills and experiences, our consultants help clients with everything from validation to process and production technology as well as quality assurance. This means that you as a consultant will have great opportunities to further develop in the area you are passionate about.

You already have a few years of experience in the industry and are confident in taking responsibility for your tasks, while also being curious to continue developing.

Your role may involve:

• Validation, qualification, and commissioning of process equipment, laboratory instruments, and computerized systems
• Quality assurance and work with quality management systems
• Improvement work within manufacturing and work processes
• Roles such as quality or process engineer, validation lead/engineer, or sub-project manager
• Contributing with a holistic view and communication skills that create understanding between technology, business, and customer
• Being part of a team where we learn from each other and develop together

You will have independent responsibility in assignments, while also having access to support from colleagues with broad experience. The role suits you who are ready to take the next step in your consulting career.

We have offices in several locations in Sweden, this position is based at our office in Kista.

This is how you will shine

You have a good ability to build relationships, communicate clearly, and focus on the customer's needs. You are solution-oriented, technically curious, and like to take the initiative to drive the work forward with energy and commitment.

We believe that you enjoy planning and structuring your work, while actively contributing to the team's collective development. You are happy to share knowledge and experiences – that’s how we grow, both as individuals and as a team.

To succeed in the role, you have:

• At least 3 years of experience working in a GMP/GxP-controlled environment within Pharma/Biotech
• A technical or natural science university degree or engineering degree
• Experience in validation, quality assurance, or technical production, preferably combined with an interest in quality and problem-solving
• You are pragmatic and solution-oriented, with a commercial mindset and a strong commitment to product quality, patient safety, and data integrity
• You have good communication skills, customer focus, and enjoy collaborating in cross-functional teams
• You express yourself fluently in both Swedish and English, in both speech and writing

Being part of Team PV

We are a consulting company passionate about being part of Life Science in Sweden. From the small startup in MedTech to the global pharmaceutical giant and everything in between. This means an opportunity to follow the entire chain – from manufacturing to use in healthcare – and work with everything from regulations and audits to project management, standards, and evaluations. Helping our clients achieve their goals is what drives us. So, if you want to be part of something bigger, something that makes a real difference and can ultimately save lives and secure patients – then you have come to the right place. With us, some of the industry's sharpest minds work, and as part of Plantvision Compliance, you will become an incredibly important cog in our constant strive to make a difference. For real.

Awards and accolades are not everything, but we are certainly proud to be a certified Great Place To Work company (for the tenth year in a row, in fact), which means we are one of the best employers in Sweden. With us, you get something different. We stand out from traditional consulting companies through our unique culture, which permeates everything we do. Inclusive, supportive, and developmental. We see you. You and your colleagues are indeed the most important thing we have.

Together we can move mountains. Today, tomorrow, and beyond.

Application

Welcome to submit your application as soon as possible. Selection and interviews are ongoing, and the position may be filled before the application deadline, which is November 30.

If you have questions about this position, please contact Ida Holmberg at 076 - 108 84 87,  [email protected] (mailto:[email protected]).

Do you have your own company and are interested in collaborating with us as a subcontractor?

Instead of applying for a specific position, please connect with us through our career page (https://plantvision.se/karriar/) and indicate that you are interested in working as a subcontractor – we will get back to you when something suitable comes up.