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. Exciting assignments that tickle the stomach await you here – assignments that require curiosity, sharp minds, and a willingness to find solutions where others see challenges. The variety 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. All of this we do together, in teams filled with some of the industry's sharpest and most experienced colleagues. Here we inspire each other, share knowledge generously, and drive development forward – with quality, curiosity, and sharpness as our common foundation.

This will be your role

You will work with our clients in both the private and public sectors, supporting them in their organizations. You will, among other things, lead projects, be involved in or drive audits, work with regulations, clinical evaluations, standards, and participate in development projects. Being a consultant in this role requires responsibility and can be challenging, but is above all very fun! The role gives you ample room to influence your own development through the assignments you work on.

The role involves:

• You will be the one guiding our clients correctly in the regulatory world.
• You will be part of the Healthcare Compliance unit.
• You will share your assignments between both the private and public sectors and see the entire chain of a medical technology product – from manufacturing to use in healthcare.
• You will take a natural place in a team that enjoys discussing quality, regulatory compliance, and project management.
• You will belong to a team that is growing, flexible, and loves to share their knowledge!

We would prefer that you live in Stockholm, but location is not decisive for the role.

This is how you will shine

We shine by sharing our knowledge, and you will do the same. Through your social and communicative skills, you create trust with the people you meet. You have the ability to make complex information easy to understand while thoroughness and quality permeate everything you do. You are independent with good self-leadership, even though you appreciate being part of a team and working with colleagues who are passionate about the same issues as you are.

To succeed in the role, you have:

• At least 4 years of experience in public operations regarding participation in procurements, organizational change, or project management.
• Experience in quality management and/or regulatory issues within medical technology/IVD or healthcare.
• A bachelor's or master's degree in Life Science (Engineering degree, Master's degree, BMA, or PhD). Alternatively, you can demonstrate equivalent experience through work life.
• High-level proficiency in both Swedish and English, both spoken and written.

It is also meritorious if you have worked with one or more of the following:

• You have worked in a medical technology department in a hospital.
• You have worked with in-house manufacturing in healthcare according to MDD/MDR or IVDD/IVDR.
• You have experience working with National Medical Information Systems (NMI).
• You have worked with the development, updating, or assessment of technical documentation related to medical technology products.
• ISO 13485, ISO 9001, ISO 27001
• You have been driving the development of requirements in procurement.

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 that can ultimately save lives and secure patients – then you have come to the right place. Here, 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 proud to be a certified Great Place To Work company (for the tenth year in a row, actually), which means we are one of the best employers in Sweden. With us, you get something different. We stand out from traditional consulting firms 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

If you believe that we are the right workplace for you and that you are the right fit for us, send in your application today! Selection is ongoing. The latest application date is December 31.

We look forward to receiving your application.

If you have questions about the position, you are warmly welcome to contact: Beatrice Orback at 076-138 52 14, [email protected]. For this recruitment, we have chosen a strategy and therefore kindly ask for no calls from recruitment, staffing, and advertising companies.

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 via 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.