82 jobs in Kista

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How many job openings are there in Kista?
We currently list 82 jobs in Kista. The average offered salary is —.
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The most common professions are Utesäljare (5), Innesäljare (5), Telefonförsäljare (4), Key account manager/KAM (4).
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JOB

Senior Validation Consultant

Do you want to help ensure quality within Life Science alongside the sharpest minds in the industry? Then this is the place for you. We offer assignments that require curiosity, problem-solving drive, and sharp expertise – 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. Your Role We're looking for a senior validation leader or expert who wants to take a central role in our most business-critical projects within Life Science. You'll be responsible for ensuring quality, regulatory compliance, and success in customer assignments – from strategy to implementation. You'll be part of Quality & Validation within our Compliance business area – a team with a strong mix of expertise and curiosity. Here you work closely with colleagues at a similar experience level, while sharing your knowledge and mentoring more junior consultants in their development. The role involves: • Ensuring that regulatory requirements and standards according to GMP/GxP are met and thereby contributing to successful, safe, and sustainable projects. • Developing validation strategies and preparing and quality-assuring validation documentation. • Qualifying and validating computerized systems in complex environments. • Driving cross-functional work with requirements definition, risk management, and quality assurance, as well as coordinating validation activities and leading resources in larger projects where close collaboration between customer and colleagues is crucial for results. • Managing deviations, CAPAs, and change requests in a structured and solution-oriented manner. • Acting as an advisor in customer projects and serving as mentor and trainer to share your experience and contribute to the team's development. We have offices in several locations in Sweden; this position is based at our office in Kista. How You'll Excel You're a confident and business-minded consultant who builds trust in customer relationships and drives work forward with structure and quality. You thrive in complex environments, take responsibility all the way to the goal, and enjoy sharing your knowledge. Combining technical depth with a solution-oriented approach comes naturally to you – as does contributing to both team and business development. To succeed in this role, you have: • University degree or equivalent in a relevant field. • At least 5 years of experience in Pharma/Biotech and working according to GMP. • Solid experience validating computerized systems (CSV). • Knowledge of GAMP and experience with systems such as eQMS/ERP/LIMS, FMS, or Historian. • Experience working according to different quality management systems and in electronic systems for document and issue management. • Very good knowledge of Swedish and English. • Experience with additional regulations and guidelines is a merit. Being Part of Team PV We're different here. We don't recruit for a specific assignment – we recruit to build our team long-term. This means we look at you, your expertise, and your development over time, and create 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. In the team, there's a strong culture of knowledge sharing, where senior consultants learn from each other and contribute to the whole. Our culture is something we're genuinely proud of. We're 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'd be soft. Application Welcome to submit your application as soon as possible. Selection and interviews are ongoing. If you have questions about this position, feel free to contact Ida Holmberg at 076 108 84 87 or [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, feel free to connect with us via our career page and indicate that you're interested in working as a subcontractor – we'll get back to you when something suitable comes up.

Vanlig anställning
Kista 21. 6. 2026 1
JOB

Life Science Consultant with Experience

Do you want to help ensure quality within Life Science alongside the industry's sharpest minds? Then this is the place for you. With us, you'll find assignments that require curiosity, drive for solutions, and sharp expertise – and give 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. Your Role You'll become part of our Life Science Compliance business area and the Quality & Validation unit – which consists of 6 teams with broad expertise in quality, validation, and production. As a consultant with us, you'll work on varying assignments where you get the opportunity to quickly build experience and develop within multiple areas you're passionate about. Examples of what you can work with: Validation, qualification, and commissioning of equipment, systems, and processes. Improvement work within manufacturing and work processes. Improving our customers' quality management systems. Roles 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 collaborate with. We have offices in several locations in Sweden; this position is based at our office in Kista. Why You'll Thrive as a Consultant with Us Here you get the best of the consultant role: Variety – different assignments, techniques, and operations Rapid Development – a steep learning curve where you build both breadth and depth Impact – you drive improvement and quality with our customers We're at the forefront of our field and work as an advisory partner. You'll see this through: Driving complex and developmental projects with our customers Educating and lecturing within our specialist areas Actively sharing knowledge – both internally and externally With us, you're always part of a community – a team where we learn from each other and senior colleagues contribute to your development. How You'll Excel You're 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 Pharma/Biotech A degree in engineering or natural sciences (university or master's level) Experience with validation or technical production, preferably combined with a strong interest in quality and problem-solving Ability to work structurally and drive work forward Very good knowledge of Swedish and English Being Part of Team PV With us, you get something different. We don't recruit for a specific assignment – we recruit to build our team long-term. This means we look at you, your expertise, and your development over time, and create the right conditions for you to continue growing. We work as an advisory partner to our customers and value long-term relationships – both externally and internally. In the team, there's a strong culture of knowledge sharing, where consultants learn from each other and contribute to the whole. Our culture is something we're genuinely proud of. We're a Great Place to Work, year after year – and we see it as proof of the environment we build together every day. And yes – if our culture had been in the walls, they would have been soft. Application Welcome to submit your application as soon as possible. Selection and interviews are ongoing. If you have questions about this position, feel free to contact Ida Holmberg at 076 - 108 84 87, [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 via our career page and indicate that you're interested in working as a subcontractor – we'll get in touch when something suitable comes up.

Vanlig anställning
Kista 21. 6. 2026 1
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