Vacant job

Do you want to ensure quality within Life Science alongside the sharpest minds in the industry? Then this is where you belong. With us, you will find assignments that require curiosity, a solution-driven mindset, and sharp competence, offering 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.

We are looking for a senior validation lead or expert who wants to take a central role in our most business-critical projects within Life Science. You are responsible for ensuring quality, regulatory compliance, and success in client assignments – from strategy to execution.

You will become part of Quality & Validation within our Compliance business area – a team with a strong mix of competence and curiosity. Here, you work closely with colleagues of similar experience levels, while sharing your knowledge and acting as a mentor to more junior consultants in their development.

The role involves:

• Ensuring that regulatory requirements and standards according to GMP/GxP are met, thereby contributing to successful, safe, and sustainable projects.

• Developing validation strategies and creating and quality-assuring validation documentation.

• Qualifying and validating computerized systems in complex environments.

• Driving cross-functional work with requirement setting, risk management, and quality assurance, as well as coordinating validation activities and leading resources in larger projects where close collaboration between client and colleagues is crucial for the result.

• Handling deviations, CAPA, and change requests in a structured and solution-oriented manner.

• Acting as an advisor in client projects and serving as a 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.

You are a confident and business-minded consultant who builds trust in client relationships and drives work forward with structure and quality.

You thrive in complex environments, take ownership all the way to the finish line, and are happy to share your knowledge. Combining technical depth with a solution-oriented approach comes naturally to you – as does contributing to both the team's and the business's development.

To succeed in the role, you have:

• A university degree or equivalent in a relevant field.

• At least 5 years of experience within Pharma/Biotech and working according to GMP.

• Extensive experience in validating computerized systems (CSV).

• Knowledge of GAMP and experience with systems such as eQMS/ERP/LIMS, FMS, or Historian.

• Experience working according to various quality management systems and in electronic document and case management systems.

• Very good proficiency in Swedish and English.

• Experience with additional regulations and guidelines is an advantage.

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 clients and value long-term relationships – both externally and internally. The team has a strong culture of knowledge sharing, where senior 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 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.

Welcome to submit your application as soon as possible. During holiday periods, it may take a little while before you hear from us; we start selection and interviews as soon as we are back from leave. If you have questions about this position, please 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 subconsultant? Instead of applying for a specific position, please connect with us via our career page and state that you are interested in working as a subconsultant – so we will contact you when something suitable arises.